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ppAt Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. /p h3The Position /h3 h3Who We Are /h3 pbAt Roche Diagnostics Solutions (RDS) /b, our mission is clear: to diagnose earlier, develop faster, and personalize treatment because every patient is unique. Within bComputational Science Informatics (CSI) /b, we are the bridge between our origin and our future, shaping the next era of human health through precise, data‑driven diagnostics and precision medicine. /p h3The Opportunity /h3 pAs a bSenior Development Engineer/Mathematician/Data Analyst /b, you will be a vital part of our development team in Spain, focusing on our innovative Blood Gas Electrolyte Analyzers. You will transform complex physical measurement data into precise, life‑saving results through mathematical excellence. /p ul liRobust Algorithms: Develop and refine sophisticated methods, algorithms, and failsafes that extract highly reliable results from physical measurement data. Drive projects from initial conception through to rigorous testing and final completion /li liModel the Future: Create mathematical models and provide expert statistical consulting (including Design of Experiments and Validation) to drive data‑driven decision‑making and product excellence /li liBridge Science and Compliance: Implement biometric methods into specification documents, ensuring our products meet the highest health authority requirements and regulatory standards /li liDrive Product Approvals: Support global product launches by developing solid statistical rationales and customized solutions for ongoing product maintenance /li liUnlock Insights: Extract, clean, and visualize large datasets, collaborating with an interdisciplinary team to present actionable insights that drive medical innovation /li liLead as a Technical Expert: Act as a central point of contact and own the technical solutions, providing the rationale necessary to ensure product quality and scientific integrity /li /ul h3Who You Are /h3 pYou are an analytical thinker, solution‑oriented who enjoys working in a team at the intersection of engineering, mathematics, physics, and medical technology. You thrive in collaborative, international environments, not hesitant to proactively raise your voice and you are passionate about using your quantitative skills to improve patient care. /p ul liQuantitative Expert: You hold a Master's degree or higher in Engineering, Mathematics, Physics, or a related quantitative field /li liExperience: You have 7+ years of professional industry related experience /li liControl Engineering/Signal Processing Specialist: You have deep knowledge of system identification, model‑based filtering, and classic or model‑predictive control methods /li liSensor Modeling Pro: You bring experience in modeling electrochemical sensors and optimizing robust calibration methods to ensure precision /li liStatistical Powerhouse: You are highly proficient in modern statistical software such as MATLAB (preferred), Python, R or JMP, with exceptional data wrangling and visualization skills /li liCollaborative Communicator: You possess the ability to translate complex mathematical results into clear, actionable insights for interdisciplinary teams /li liRegulatory Minded: You have an affinity for medical technology and an interest in—or experience with—analytical performance guidelines (such as CLSI) /li liCommunication Skills: Fluent English is required /li /ul ul liThis is an on‑site position and no relocation assistance is provided /li /ul pReady to help us lead the way in healthcare? Together, we’ll create a healthier, brighter future for all. /p pA healthier future drives us to innovate. Together, more than 100,000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life‑changing healthcare solutions that make a global impact. /p pLet’s build a healthier future, together. /p pRoche is an Equal Opportunity Employer. /p /p #J-18808-Ljbffr

pINBRAIN NEUROELECTRONICS in Bellaterra is seeking a Manufacturing and Testing Technician to support fabrication and testing of samples for process development within a regulated semiconductor environment for medical devices. /ppThe role requires a technical bachelor’s degree, 2+ years in manufacturing, and fluency in English. You will work with thin films and semiconductor assembly, ensuring quality and regulatory compliance while supporting supply chain needs. /p #J-18808-Ljbffr

ppAt Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. /ppShape the Future of Secure Engineering with Roche. Are you ready to tackle bold challenges and make a real impact? At Roche, we’re not just building IT infrastructure — we’re engineering secure, scalable, and highly innovative software solutions that protect and empower digital health systems globally. We’re looking for passionate and driven individuals to join our Certman PKI (Public Key Infrastructure) team as a Software Engineer and help us lead the way in cutting‑edge, trust‑based technology. /ph3Who We Are /h3pA Better Tomorrow Starts Today. At Roche, everything we do is powered by our passion to transform patients’ lives. We embrace science, ethics, and innovation. We're bold in our decisions and actions because we know a brighter future depends on it. Every day, we build that future — for a better world, for humankind. Diversity and inclusion aren’t just buzzwords here; they’re essential to who we are. We believe that unique perspectives breed innovation and creativity, which is why we are committed to building teams that reflect the extraordinary range of human potential. /ph3Your Role /h3pRedefine Excellence in Secure Software Engineering. As a Software Engineer within Roche’s Certman PKI team, you will become a driving force behind the design, development, and evolution of our mission‑critical enterprise trust and identity software. Working closely with the latest technology trends, you will build the software layer that manages digital certificate lifecycles, cryptographic keys, and secure authentication. /ppA Key Element of Your Contribution: As an experienced C# engineer, you will design and deliver high‑performance, resilient software services that power Roche’s global operations. This role demands deep expertise across the full .NET stack — from advanced memory management and asynchronous programming patterns to designing secure, scalable backend systems and orchestrating containerized microservices across AWS and Kubernetes at enterprise scale. You’ll apply asynchronous programming practices and design excellence to build high‑throughput, low‑latency APIs that meet the reliability and compliance requirements of medical devices serving patients worldwide. Your commitment to software engineering excellence, clean code principles, and robust design patterns will be fundamental to delivering seamless and secure experiences that uphold Roche’s standards of quality and trust. /ph3What You’ll Do /h3pAs a Software Engineer in the Certman PKI team, you will play a critical role in designing, building, and evolving our certificate issuance API using ASP.NET Core (C#). You will own the end‑to‑end quality of the service. You will design and implement well‑versioned REST APIs, automate cryptographic and certificate lifecycle workflows, and diagnose and resolve complex performance, concurrency, or architectural bottlenecks using profiling and observability tooling. You will deploy and operate our services natively on AWS and AliCloud, working hands‑on with EKS/Kubernetes, KMS for key operations, EC2, IAM, and other core AWS building blocks. You will own and continuously improve our CI/CD pipelines on GitLab and GitHub Actions — building reproducible, secure, and fully automated build, test, scan, and deploy workflows for containerized .NET services. This role involves writing clean, testable, well‑covered code, conducting meaningful peer code reviews, and applying secure‑by‑default best practices across the PKI landscape. You will write technical software documentation, design decisions, and operational runbooks to drive ongoing engineering excellence. You’ll also contribute to building a strong, collaborative, and agile engineering culture. /ph3Your Opportunity to Shine /h3pThis role is about taking ownership and leading the charge toward transformational software architecture, precision engineering, and cutting‑edge cloud integration. Show your skills, grow your career, and make a measurable impact on enterprise security — all alongside a team that has your back. /ph3Why Choose This Role? /h3pAt Roche, you're more than just an employee — you're part of a mission‑driven global team that celebrates diversity, creativity, and modern engineering through inclusion and innovation. Beyond that foundation, you'll find significant growth opportunities to expand your technical horizons in both advanced enterprise security and cloud‑native software engineering, sharpen your architectural skills, and explore exciting, global challenges at the intersection of IT and life sciences. Finally, you'll work in a dynamic environment where no two days are the same, making it an ideal opportunity if you thrive on solving complex, real‑world software and automation problems. /ppReady to elevate your career while playing a pivotal role in saving lives? Join Roche, where your work meets purpose — our shared commitment ensures our software (and teams) are always striving for excellence. /ph3Equal Opportunity Employer /h3pRoche is an Equal Opportunity Employer. We believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future. We are passionate about transforming patients’ lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. We are proud of who we are, what we do, and how we do it. We are many, working as one across functions, across companies, and across the world. We are Roche. /p /p #J-18808-Ljbffr

Principal Data Engineer / Data LeadCandidatar-selocations: Sant Cugat del Vallès: Poznan: Warsaw: Penzbergtime type: Tempo integralposted on: Publicado hojejob requisition id: Na Roche, você pode-se apresentar como você mesmo, abraçado pelas qualidades únicas que traz. Nossa cultura incentiva a expressão pessoal, o diálogo aberto e as conexões genuínas, onde você é valorizado e respeitado por quem você é, e permitindo que você prospere tanto pessoal como profissionalmente. É assim que pretendemos prevenir, deter e curar doenças e garantir que todos tenham acesso aos cuidados de saúde hoje e nas gerações futuras. Junte-se à Roche, onde cada voz é importante.### A posiçãoWho We Are We are seeking an exceptionally skilled and influential Principal Data Engineer / Data Leadto join and provide technical leadership for the digital solution navify Cervical Screening. You will be a top-tier expert, driving architectural decisions, overseeing data integration and ensuring delivery of features and improvements. This is a critical leadership role for someone who is passionate about data, delivery and technical excellence.As Data Lead, you will provide orchestration within cross-functional agile product teams, influencing the strategic direction and delivery of data-driven features. While hands-on contributions are expected, your primary focus as a Data Lead will be on ensuring the strategic differentiation of products through data and innovation, orchestrating DAR capabilities.Key Responsibilities Drive data integration and data fabric adoption across the domains, bringing together data, business and development domains. Ensure best practices and support organization-wide standards for data quality, governance, security, and observability. Act as a technical subject matter expert, mentoring Senior and Staff Engineers and collaborating closely with engineering leadership, data scientists, and business stakeholders. Partner with cross-functional stakeholders to shape data strategy, translate business needs into scalable technical solutions, and influence decision-making at both domain and enterprise levels. Spearhead the evaluation and integration of new technologies to continuously improve the performance and reliability of the data ecosystem. Troubleshoot and resolve the most complex performance and architectural challenges across the data ecosystem. You will be accountable for defining and ensuring timely delivery of all data-related requirements, including data integration, migration, storage, structure, legal compliance, privacy, quality, and insights generation. You will orchestrate DAR engagement and delivery for digital products, activating the right DAR capabilities. You will act as a key liaison, building and maintaining strong working relationships with cross-functional experts (other data experts, product owners, software engineers, clinicians) to jointly explore business opportunities and data assets.Required Qualifications 8+ years of professional experience in a Data Engineering role, with significant experience operating at a Principal or Staff-level capacity. Expert proficiency in SQL and Python. Extensive experience architecting and managing large-scale cloud data platforms (e.g., AWS Glue, Google Dataflow, Azure Data Factory) and deep expertise in containerization and orchestration (Docker/Kubernetes). Deep, hands-on expertise in data warehousing concepts, advanced modeling techniques (e.g., dimensional modeling, data vault), and establishing data governance frameworks. Proven track record of building, optimizing, and leading the deployment of massive-scale, highly concurrent data pipelines using distributed processing frameworks (e.g., Apache Spark, Flink). Exceptional communication, negotiation, and influencing skills, with the ability to present complex technical concepts to both technical and executive audiences.Preferred Qualifications Good command of Spanish. Deep experience with workflow orchestration tools (e.g., Apache Airflow, Dagster) and managing them at scale. Experience with NoSQL and graph databases (e.g., MongoDB, Cassandra, Neo4j). Expertise in stream processing architectures and technologies (e.g., Kafka, Kinesis, Pulsar).* Extensive experience with Terraform, CloudFormation, or other advanced Infrastructure as Code (IaC) tools and GitOps methodologies.Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Sant Cugat del Vallès. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process.### Quem nós somosUm futuro mais saudável nos leva a inovar. Juntos, mais de 100 mil funcionários em todo o mundo se dedicam ao avanço da ciência, garantindo que todos tenham acesso à saúde hoje e nas próximas gerações. Nossos esforços resultam em mais de 26 milhões de pessoas tratadas com nossos medicamentos e mais de 30 bilhões de testes realizados usando nossos produtos de diagnóstico. Nós nos capacitamos para explorar novas possibilidades, promover a criatividade e manter as nossas ambições altas, para fornecer soluções de saúde que mudem a vida e causem um impacto global.Vamos construir juntos um futuro mais saudável.A Roche é um empregador que pratica políticas de igualdade de oportunidades.### About UsAcreditamos ser necessário oferecer soluções médicas agora – mesmo quando desenvolvemos inovações para o futuro. Nosso compromisso é transformar a vida dos pacientes. Temos coragem para decidir e agir. Acreditamos também que bons negócios significam um mundo melhor. É para isso que trabalhamos diariamente. Temos compromissos com o rigor científico, com a ética e com o acesso a inovações médicas para todos. Fazemos isso hoje para construir um amanhã melhor. Temos orgulho de quem somos, do que fazemos e de como fazemos. Somos muitos, trabalhando como um em todo o mundo. Somos Roche. br#J-18808-Ljbffr

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position Who We Are We are seeking an exceptionally skilled and influential Principal Data Engineer to join and provide technical leadership for the digital solution navify Cervical Screening. You will be a top-tier expert, driving architectural decisions, overseeing data integration and ensuring delivery of features and improvements. This is a critical leadership role for someone who is passionate about data, delivery and technical excellence. As Data Lead, you will provide orchestration within cross-functional agile product teams, influencing the strategic direction and delivery of data-driven features. While hands-on contributions are expected, your primary focus as a Data Lead will be on ensuring the strategic differentiation of products through data and innovation, orchestrating DA&R capabilities. Key Responsibilities - Drive data integration and data fabric adoption across the domains, bringing together data, business and development domains. - Ensure best practices and support organization-wide standards for data quality, governance, security, and observability. - Act as a technical subject matter expert, mentoring Senior and Staff Engineers and collaborating closely with engineering leadership, data scientists, and business stakeholders. - Partner with cross-functional stakeholders to shape data strategy, translate business needs into scalable technical solutions, and influence decision-making at both domain and enterprise levels. - Spearhead the evaluation and integration of new technologies to continuously improve the performance and reliability of the data ecosystem. - Troubleshoot and resolve the most complex performance and architectural challenges across the data ecosystem. - You will be accountable for defining and ensuring timely delivery of all data-related requirements, including data integration, migration, storage, structure, legal compliance, privacy, quality, and insights generation. - You will orchestrate DA&R engagement and delivery for digital products, activating the right DA&R capabilities. You will act as a key liaison, building and maintaining strong working relationships with cross-functional experts (other data experts, product owners, software engineers, clinicians) to jointly explore business opportunities and data assets. Required Qualifications - 8+ years of professional experience in a Data Engineering role, with significant experience operating at a Principal or Staff-level capacity. - Expert proficiency in SQL and Python. - Extensive experience architecting and managing large-scale cloud data platforms (e.g., AWS Glue, Google Dataflow, Azure Data Factory) and deep expertise in containerization and orchestration (Docker/Kubernetes). - Deep, hands-on expertise in data warehousing concepts, advanced modeling techniques (e.g., dimensional modeling, data vault), and establishing data governance frameworks. - Proven track record of building, optimizing, and leading the deployment of massive-scale, highly concurrent data pipelines using distributed processing frameworks (e.g., Apache Spark, Flink). - Exceptional communication, negotiation, and influencing skills, with the ability to present complex technical concepts to both technical and executive audiences. Preferred Qualifications - Good command of Spanish. - Deep experience with workflow orchestration tools (e.g., Apache Airflow, Dagster) and managing them at scale. - Experience with NoSQL and graph databases (e.g., MongoDB, Cassandra, Neo4j). - Expertise in stream processing architectures and technologies (e.g., Kafka, Kinesis, Pulsar). - Extensive experience with Terraform, CloudFormation, or other advanced Infrastructure as Code (IaC) tools and GitOps methodologies. Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Sant Cugat del Vallès. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process. Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer.

ph3Role Overview /h3 pWe’re looking to bring a Software Developer (Electronic Invoicing) to join a small, technically focused team building and maintaining a B2B electronic invoicing platform. We work with international standards and integrate with national tax systems worldwide. In this role, you’ll take end-to-end ownership of backend systems — from design and implementation to production operations. /p h3About B2Brouter /h3 pB2Brouter is a leading European provider of electronic document exchange solutions, specializing in e-invoicing, e-procurement, and B2B data integration. We help companies automate, secure, and optimize their electronic transactions through reliable, scalable, and compliant digital platforms. /p h3Key Responsibilities /h3 ul liDesign, build, and maintain REST APIs for invoice processing, document exchange, and third-party integrations. /li liDevelop and manage asynchronous processing pipelines using background jobs and queue systems. /li liBuild and maintain integrations with external platforms, including government tax authorities and document exchange networks. /li liOptimize database queries, ensure data consistency, and manage concurrency in high-throughput environments. /li liParticipate in code reviews, technical discussions, and contribute to backend architecture decisions. /li liSupport production operations, including incident response, monitoring, and troubleshooting. /li liWrite and maintain technical documentation (systems, APIs, integration specs, and operational runbooks). /li /ul h3Required Skills Qualifications /h3 ul li4+ years of experience developing with Ruby on Rails in production environments. /li liStrong experience designing and maintaining RESTful APIs. /li liHands‑on experience with background job/queue systems and asynchronous workflows. /li liSolid SQL knowledge and experience in database performance tuning optimization. /li liComfortable working with XML-based formats and transformations (e.g., XML, XSLT) as well as JSON. /li liProven ability to work with third‑party integrations and external dependencies. /li liEnglish proficiency, as technical documentation, standards, and specifications are primarily in English. /li liFamiliarity with modern development workflows: Git and CI/CD. /li /ul h3Valuable / Nice‑to‑Have Skills /h3 ul liKnowledge of Redis and caching strategies. /li liExperience with observability tools: logging, monitoring, metrics, alerting. /li liUnderstanding of security best practices for APIs (auth, data protection, auditability). /li liExperience working in high‑availability / high‑throughput backend environments. /li liExperience in electronic invoicing standards and structured formats (e.g., UBL, CII, Factur‑X/ZUGFeRD, etc.). /li liExperience integrating with government tax authority systems (clearance/reporting models). /li /ul h3What We Offer /h3 ul liOpportunity to work in a fast‑growing international SaaS company, building a product used by businesses across multiple markets. /li liExposure to European and global digital transformation projects, working with international e‑invoicing standards and integrations with tax authorities. /li liA collaborative, innovative, and supportive team culture, with strong technical ownership and knowledge sharing. /li /ul pB2Brouter simplifies electronic invoicing and document exchange for businesses of all sizes. Our cloud‑based platform helps companies connect with public administrations and private companies ensuring compliance and saving time through fully digital and secure processes. /p /p #J-18808-Ljbffr

Experteer Overview As Software Engineer in Roche’s Certman PKI team, you shape secure, enterprise-grade software that manages certificates, keys, and authentication for health systems. You’ll design and evolve an API-driven certificate issuance platform, collaborating across a security-conscious organization. Expect work on high-performance, scalable services deployed in cloud environments with a strong emphasis on reliability and compliance. You’ll grow your skills in modern tech while contributing to Roche’s mission to improve global health and trust in digital health solutions. Compensaciones / Beneficios • Design, build, and evolve the certificate issuance API (ASP.NET Core, C#) • Own end-to-end quality of REST services and ensure secure-by-default practices • Automate cryptographic and certificate lifecycle workflows • Diagnose performance, concurrency, and architectural bottlenecks using profiling and observability tools • Deploy and operate services on AWS and AliCloud with Kubernetes (EKS) • Own and improve CI/CD pipelines (GitLab, GitHub Actions) for containerized .NET services • Write clean, testable code and perform peer reviews; produce technical docs and runbooks • Contribute to a collaborative, agile engineering culture Responsabilidades • Experienced C# engineer with deep .NET stack expertise • Design secure, scalable backend systems and REST APIs • Experience with AWS, Kubernetes, containerized microservices • Knowledge of cryptography, certificate lifecycle management, and PKI concepts • Familiarity with CI/CD pipelines (GitLab, GitHub Actions) and cloud-native deployment • Focus on quality, performance, and security in software development • Ability to document decisions and operate runbooks Requisitos principales •

ppAt Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. /p h3The Position /h3 h3What will your main responsibilities be? /h3 ul liInternal advisory: Support the resolution of employee queries related to the collective bargaining agreement, employment rights, leave policies, vacation entitlements, and Spanish labour legislation /li liEmployee and labour relations: Assist in the preparation of documentation and reports for Employee Representatives (Works Council), labour inspections, and collective bargaining processes. Prepare meeting minutes and presentations related to employment and labour relations topics /li liCase management and compliance: Support the administration and follow-up of disciplinary processes, organisational restructuring initiatives, administrative conciliation procedures, and employment litigation matters, while ensuring compliance with Spanish labour legislation and internal policies /li liReporting and international projects: Prepare labour relations reports and documentation in English, contributing to the monitoring of key metrics and supporting the global People Culture team /li /ul h3What are we looking for? /h3 ul liEducation: You are currently pursuing a Bachelor's degree in Labour Relations and Human Resources, Law, or a Master's/Postgraduate qualification specialising in Labour Law or Employment Law in Spain /li liLanguages: Fluent English (minimum B2/C1 level), both written and spoken, with the ability to collaborate with international teams and interpret corporate documentation /li liEligibility: You must be eligible to sign an internship agreement (Convenio de Prácticas) with a university or educational institution in Spain /li liKey competencies: Strong attention to detail, analytical mindset, ability to handle confidential information with discretion, excellent communication skills, and a proactive attitude /li liTechnical skills: Proficiency in Microsoft Office (particularly Excel and PowerPoint). Knowledge of HR systems such as Workday will be considered an advantage /li /ul h3Who we are /h3 pA healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. /p pLet’s build a healthier future, together. /p pbRoche is an Equal Opportunity Employer. /b /p /p #J-18808-Ljbffr

pBlackBerry Inc. is seeking a skilled IT Administrator to manage and optimize IT infrastructure at our new office in Sant Quirze del Vallès, Barcelona. You will work closely with team members in Zurich to ensure smooth operations and compliance with corporate IT policies. /ppThe ideal candidate has over 5 years of experience in IT administration and valid cybersecurity certification. Join us to contribute to innovative robotics solutions and enjoy flexible work arrangements and career development opportunities. /p #J-18808-Ljbffr

pGrifols seeks a Pharmacovigilance professional to provide operational support for global PV activities, ensuring high-quality safety data analysis, data review, and regulatory deliverables across investigational and marketed products. /ppThe role includes safety data extraction, development of safety reports, and collaboration with Regulatory Affairs, IT, and QA to maintain compliance. Strong Excel/SQL skills and English fluency are required. /p #J-18808-Ljbffr

ppChez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement. Voici comment nous visons à prévenir, arrêter et guérir les maladies et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Rejoignez Roche, où chaque voix compte. /ph3La position /h3pbGPC Training and Service Quality Lead /b /ppbDepartment: /b Global Patient Care (GPC)brbArea: /b Global Customer Support (GCS)brbReports to: /b GPC Support LeadbrbLocation: /b Sant Cugat, Spain /ppbAbout the Role /b /ppThe Training and Service Quality Lead for Global Patient Care (GPC) plays a pivotal role in shaping service excellence across Roche Diagnostics' customer support network. Leading a dedicated team of Training and Service Quality Specialists, this role ensures the development and implementation of robust training programs and quality assurance frameworks that enable consistent, high-quality, patient-centered care. /ppCollaborating closely with GPC leadership, you will drive strategies that enhance skill development, align with global service standards, and foster a culture of continuous improvement while ensuring compliance with regulatory and quality standards. Through effective leadership and data-driven insights, you will strengthen the quality and efficiency of interactions with patients and customers, advancing Roche's mission to deliver transformative healthcare solutions. /ppbYour Responsibilities /b /ppbStrategic Program Development: /b /pullipIdentify training and service quality improvement opportunities by collaborating with regional Customer Support hubs, Business Implementation Specialists, and other GPC functions to ensure services evolve with business needs /p /lilipDesign, enhance, or discontinue training and quality programs to uphold service excellence while ensuring compliance with auditable training standards /p /lilipLead projects related to improvements and changes within Global Patient Care to meet evolving business needs /p /li /ulpbCustomer Experience Operational Excellence: /b /pullipEstablish and continuously improve a global training and service quality framework to deliver consistent, high-standard customer and patient experiences /p /lilipDefine and implement operational standards to ensure excellence in Training and Service Quality across all regions /p /lilipImplement a robust quality monitoring framework for external Customer Support operations /p /lilipUtilize customer satisfaction metrics, feedback, and operational data to identify trends and improvement areas /p /li /ulpbTraining Program Design and Delivery: /b /pullipLead the development and execution of training programs tailored to enhance competencies of frontline teams and specialists /p /lilipEnsure training initiatives align with global service delivery objectives and support achievement of organizational KPIs /p /lilipWork with external partners to define and implement global training standards /p /li /ulpbQuality Assurance Compliance: /b /pullipImplement a robust quality assurance framework to monitor and improve interactions with patients and customers /p /lilipEnsure compliance with global standards for CRM systems, contact center operations, and regulatory requirements /p /lilipReport directly to GPC Leadership to guarantee consistent, high-standard experiences while supporting delivery of Roche's innovative products and digital solutions /p /li /ulpbKPI Management Analysis: /b /pullipTrack, analyze, and report key performance indicators related to training effectiveness and service quality /p /lilipProvide actionable insights to leadership teams and regional operations to drive continuous improvement /p /li /ulpbTeam Leadership Development: /b /pullipFoster a culture of excellence, inclusivity, and collaboration while driving team and individual performance /p /lilipLead by example as a VACC (Visionary, Architect, Catalyst, Coach) leader; set clear goals, provide continuous guidance, motivation, coaching, and feedback /p /lilipCultivate an inspiring, inclusive team environment that promotes diversity and cross-functional collaboration; overcome multi-location challenges proactively /p /lilipEnable exceptional customer service while optimizing efficiency and effectiveness; strive for continuous improvement in all areas of Customer Care /p /lilipDrive talent acquisition and hiring processes; focus on retention by maintaining low attrition and providing a positive work environment /p /lilipProvide proactive feedback, coaching, performance evaluations, and support compensation reviews; contribute to succession planning and talent management /p /lilipManage employee performance, address conflicts, and implement performance improvement plans as necessary; ensure adherence to HR and compliance policies /p /li /ulpbStakeholder Collaboration: /b /pullipCollaborate with regional Customer Support hubs, Business Implementation Specialists, and other Support Functions to identify training needs and quality assurance opportunities /p /lilipProvide insights that inform decision-making and promote strategic alignment across regions /p /lilipSupport Supplier Operation Manager in planning, managing, and controlling business processes related to external Partner Management /p /li /ulpbYour Experience Skills /b /ppbRequired: /b /pullipUniversity Degree/Bachelor's or equivalent postgraduate qualification /p /lilipMinimum 3–5 years in Customer Care Management, Training Management, Quality Management, or related roles in a regulated environment /p /lilipProven excellent people management and coaching skills with a VACC leadership mindset /p /lilipProven experience implementing global training and QA frameworks in a multi-regional context /p /lilipAbility to understand, explain, follow, and enforce SOPs, Contact Center KPIs, and protocols /p /lilipExperience leading, inspiring, and developing high-performing teams while managing operations during strategic transformation /p /lilipProject Management experience, preferably with Agile Methodology knowledge /p /lilipChange Management experience /p /lilipFluent command of English; other languages based on local/regional needs /p /lilipExcellent customer service, communication, and organizational skills /p /lilipAbility to de-escalate and resolve customer complaints effectively /p /lilipExperience building business cases and presenting to stakeholders /p /lilipEffective negotiation skills /p /lilipExperience working with executive stakeholders /p /lilipExcellent IT navigation skills; fast learner of new technologies /p /lilipResult-oriented, customer-centric, service-oriented with a growth mindset; enjoys diverse, inclusive, intercultural environments /p /lilipFlexibility to travel /p /li /ulpbPreferred: /b /pullipExperience in product quality management and compliance /p /lilipSupplier management experience /p /lilipDigital solutions and healthcare industry experience in a contact center /p /lilipKnowledge and expertise in the diabetes therapeutic area and use of technology-based solutions in healthcare /p /li /ulpbWho we are /bbrA healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. /ppbrLet’s build a healthier future, together. /ph3Qui nous sommes /h3pUn avenir plus sain nous pousse à innover. Ensemble, plus de 100 000 employés à travers le monde sont dédiés à faire progresser la science et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Nos efforts aboutissent à plus de 26 millions de personnes traitées avec nos médicaments et plus de 30 milliards de tests réalisés avec nos produits de Diagnostique. Nous nous encourageons mutuellement à explorer de nouvelles possibilités, à favoriser la créativité et à conserver nos grandes ambitions, afin de fournir des solutions de santé qui changent des vies et ont un impact mondial. /ppConstruisons ensemble un avenir plus sain. /ppbRoche est un employeur offrant l'équité en matière d'emploi. /b /p /p #J-18808-Ljbffr

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position About Our Team We at Global Diagnostics Procurement (DOP) are a team of about 200 enthusiastic professionals, committed to driving value with our suppliers worldwide. From locations around the world and with a diverse and multicultural team, we source, manage our supplier base, develop & execute category strategies and constantly develop & digitize processes that enable us to best support our business to grow sustainably. If you aspire to make an impact and want to be part of a high performing and world-class Procurement team, this is for you. We are DOP. At Roche, we do now what patients need next. The Opportunity Are you ready to architect the global digital process landscape and lead the strategic optimization of systems that drive our end-to-end global procurement operations? As our Business Capability Lead (BCL) located in Sant Cugat, Spain, you will take strategic and operational ownership over critical segments of the global Demand-to-Pay process landscape. In this high-impact role, you will define process governance, integrate complex interfaces across corporate ecosystems, and serve as a vital change agent to accelerate the myBuy solution adoption across the enterprise. myBuy is Roche's digital procurement platform, designed to enhance the procure-to-pay process by providing transparency, timely transactions, and automation for our buying operations. - Reporting Line: Reports directly to our Sourcing Lead and is part of the Procurement Center of Excellence (CoE). - Wider team and stakeholders: Leads a global Business Capability Community formed by SMEs. You will manage cross-functional relationships across the DOP Leadership Team (DPLT), CoE LT, DOP Delivery, DOP Sourcing Teams, RSS Demand to Pay, Global Procurement, and external technology providers. - Role Type: As BCL, you represent DOP`s business interests globally in relevant forums, and you are responsible for the development and continuous improvement of DOP`s procure-to-pay strategy. - Impact: You drive global operational efficiency, process compliance, and large-scale digital adoption. Specifically, you are accountable for: - Process Design & Strategy: Developing and deploying the DOP roadmap for myBuy, in alignment with functional partners like DIA Global Supply Chain and RSS Demand to Pay. - Automation & Innovation: Proactively identifying opportunities for process automation and digitalization in close collaboration with Delivery, Category, Digital & Process Management, and RSS Demand to Pay. - SME Analysis & Governance: Acting as a deep subject matter expert to analyze, elaborate options, and design solutions that resolve process, system, performance indicator, or data concerns, while supporting data and rule definitions. - Transformation Project Delegation: Serving as a responsible delegate on major corporate initiatives (such as the ASPIRE program; our overarching process and digital transformation) to support global template adoption and evaluate localized change impacts. - Continuous Improvement: Leading continuous improvement initiatives, managing global requirement alignment, and partnering with fellow BCLs and Business Capability Owners (BCOs) to optimize end-to-end cross-functional performance. - Community & ARTS Representation: Leading the Business Capability Community of SMEs and representing DOP in communities and Agile Release Trains (ARTs). - Knowledge Management: Governing the development, structural maintenance, and delivery of global system process documentation and training materials. - Conflict & Exposure: Resolving matrix conflicts regarding competing project priorities or process expectations, while delivering high-frequency monthly or quarterly KPI updates (such as cycle times and compliance) to the CoE LT and DPLT. Who you are We look for process-driven champions with an entrepreneurial mindset who can lead collaborative communities and remove friction from digital operations. - Education: University degree with a business or life sciences focus is required; a Master's degree (MBA or equivalent) and professional certifications (such as CIPS) are highly preferred. - Experience: Deep expert knowledge of procurement systems and enterprise architectures (e.g., SAP S/4HANA, GEP Smart / GEP Nexxe), coupled with a robust understanding of the broader procurement technology provider landscape. - Process Expertise: Extensive experience in the design, management, and continuous improvement of complex business processes, with distinct experience operating within the Demand-to-Pay landscape. - AI & Digitalization: Advanced knowledge in AI application and a strong affinity to explore AI-driven solutions broadly, particularly regarding the digital transformation of operations (Digital 2.0 / Industry 4.0). - Change & Stakeholder Management: Proven track record of guiding stakeholder groups, managing escalations, navigating communication lines, and leading cross-functional project teams without direct headcount authority. - Mindset & Soft Skills: A self-organized, motivated professional with a solution-oriented "Can-Do" attitude and an end-to-end business perspective. You possess excellent negotiation and conflict resolution skills, acting as a customer-oriented partner who champions an open speak-up and error culture. - Languages: Business-level fluency in English is required; German language skills are a strong asset. Ready for the next step? We look forward to hearing from you. Apply now to discover this exciting opportunity! Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer.

ph3Responsibilities /h3 ul liAct as key operational partner for regulatory compliance for sustainability. /li liDrive day-to-day execution and provide regulatory insights. /li liEnsure global compliance of HP products with environmental regulations and market access requirements. /li liMaintain visibility on regulations, trends, implementation status, risks, and challenges across regions. /li liPrepare and support monthly compliance reviews and reporting. /li liTrack and resolve off-track items, driving actions and mitigation plans. /li liSupport the development and quality of Working Assumptions and regulatory interpretations. /li liAct as packaging sustainability SME for customer inquiries and requirements. /li liCollaborate with HP product stewards to set and drive HP’s sustainability strategies and goals across functions. /li liMonitor industry trends, technologies, and competitor landscape. /li /ul h3Requirements /h3 ul liBachelor's or Master's degree in sustainability, Environmental Science or related field. /li liKnowledge and understanding of sustainability topics (ESG, recycling, circular economy, etc.) /li liStrong project management skills /li liUsing data and AI tools /li liTypically, 2+ years’ experience in packaging design, sustainability, compliance or with relevant work experience. /li liDesirable: experience/specialist knowledge of Extended Producer Responsibility (including WEEE and Batteries), Packaging or Product Repair Longevity /li liProven project management skills to lead projects and programs with team members from diverse technical backgrounds. /li liAbility to collaborate successfully, coordinating and directing virtual, matrixed teams and resources to manage multiple projects and deadlines, and solve complex problems. /li liEffective written and verbal communication skills; mastery of English. /li liWillingness to thrive in an ambiguous and dynamic environment. /li liExcellent data analysis and problem-solving skills. /li liSelf‑motivated to make progress towards goals autonomously as needed. /li liAbility to balance multiple projects and meet deadlines. /li liExperience or understanding of productivity software and tools, including AI, Power BI, Microsoft Word, PowerPoint, Excel, SharePoint, and Teams. /li liAbility to effectively communicate program plans, proposals, results, and requests at the senior management level. /li /ul /p #J-18808-Ljbffr

ppYour role mission: Provides operational support for global pharmacovigilance activities for Grifols investigational and marketed products. Ensures pharmacovigilance deliverables are of the highest quality and meet global regulatory reporting timelines. Responsible for data reviews and management of the integrated database utilized by worldwide Grifols pharmacovigilance personnel. /p h3What your responsibilities will be /h3 ul liParticipate in safety data collection, review, processing, evaluation, analysis and compilation. /li liProcess adverse event case reports for marketed products, define required submissions, and conduct follow‑up with reporters. /li liCompile and reconcile information to prepare documentation required by pharmacovigilance legislation. /li liReview weekly literature and updates in pharmacovigilance legislation, ensure compliance with archiving tasks, and compile information for periodic safety update reports. /li liEnsure quality and compliance with legal requirements, support staff in audits and inspections, provide training, and support review and update of SOPs. /li liPerform PV database operating activities: query data extraction, ensure data consistency and integrity, and support updates in database configuration. /li /ul h3Who you are /h3 ul liBachelor's degree in Health Sciences (Pharmacy, Biology, Chemistry). A Master's or Postgraduate degree in the pharmaceutical sector and/or in Pharmacovigilance is valuable. /li li1–2 years of experience in a similar position within the pharma industry (CRO or pharmaceutical company), highly valued. /li liKnowledge of MS Office and SAP. /li liAdvanced level of English. /li /ul h3Benefits package /h3 pSchedule: Monday‑Thursday 7‑10 to 16‑19h and Friday 8‑15h (with the same flexible start time). /p pContract of Employment: Permanent position. /p pGrifols is an equal opportunity employer. /p /p #J-18808-Ljbffr

ph3Company Culture /h3pAt Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. We aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. /ph3Position Overview /h3pThe Position At Roche, we believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future. We are passionate about transforming patients’ lives and we are brave in both decision and action. And we believe that good business means a better world. Join Our Team: Make a Difference in International Regulatory Affairs! /ppRoche is seeking a dynamic and highly motivated individual to join our team as an International Regulatory Affairs Professional. We are looking for candidates who bring an innovative and creative mindset to the table, along with a proven track record in the Regulatory Affairs field. If you are passionate about making a positive impact on global healthcare through regulatory excellence, we invite you to be part of our dedicated team. /ph3Key Responsibilities /h3ulliLeading and supporting regulatory strategies for global IVD/MD instruments and software submissions /liliEnsuring compliance with international regulatory requirements and standards /liliCollaborating with cross-functional teams, including RD, Quality, and Clinical, to drive regulatory initiatives /liliProviding regulatory guidance to support product development and lifecycle management /liliStaying abreast of evolving regulatory trends and updates, and implementing best practices /li /ulh3Requirements /h3ulliBachelor’s Degree in Life Sciences, Regulatory Affairs, or a related field /lili5 to 7 years of experience in Regulatory Affairs (Regulatory, RD, Quality and/or Clinical), with some experience in healthcare regulatory affairs /liliIn-depth knowledge of global regulatory requirements, guidelines, and procedures especially for IVD instruments software /liliStrong organizational and communication skills /liliAbility to multitask and effectively manage multiple projects simultaneously /liliSelf‑motivated and capable of working independently in a self‑management environment /liliExperience in IVD instrument and/or software development /li /ulh3Benefits /h3ulliCollaborative and innovative work environment /liliOpportunity to make a meaningful impact on patients' lives globally /liliCompetitive compensation and benefits package /liliProfessional development and growth opportunities within a leading global healthcare organization /li /ulpRoche is an Equal Opportunity Employer. /p /p #J-18808-Ljbffr

ppWould you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well‑being of people around the world. We are leaders in plasma‑derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. /p pWe believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding. /p h3Mission /h3 pProvides operational support for global Pharmacovigilance (PV) activities for Grifols investigational and marketed products. Ensures Drug Safety, Pharmacovigilance deliverables are of the highest quality and meet global Regulatory Reporting timelines. Responsible for Safety Data Analysis, Data Review, and management of the integrated Safety Database utilized by worldwide Grifols pharmacovigilance personnel. /p h3What Your Responsibilities Will Be /h3 ul liParticipate in the safety data collection, review, processing, evaluation, analysis and compilation: ul liExtraction, review and analysis of information from the pharmacovigilance database, performing Safety Information Analytics, Safety Data Analysis, Data Extraction, Data Review, and Data Management. /li /ul /li liCompilation and reconciliation of information in order to prepare documentation required by pharmacovigilance legislation: ul liProcess and review safety data to develop Aggregate Safety Reports. /li liSupport responses to requests from regulatory agencies, ensuring Regulatory Compliance. /li liCoordinate and manage creation of SQL queries for Data Extraction used in different PV documents. /li liDevelop training documentation and/or work instructions to determine methods and procedures. /li liWork as Signal Analyst during Signal Detection and Signal Management activities, including extraction of signal detection reports and ensuring document filing and archiving. /li /ul /li liEnsure quality and compliance with the legal requirements for pharmacovigilance tasks and responsibilities: ul liSupport pharmacovigilance staff involved in audits and inspections (Quality Assurance, GVP Compliance). /li liProvide training to concerned personnel based on the training plan. /li liSupport the review and update of SOPs. /li liInteract with Regulatory Affairs Department regarding Aggregate Safety Reports and other documents required by Regulatory Authorities. /li /ul /li liPV database operating activities: ul liUse SQL queries for Data Extraction for different PV documents. /li liEnsure Data Consistency, Data Integrity, and Data Quality within the Safety Database. /li liSupport updates in the database configuration, collaborating with IT and Database Administration activities. /li /ul /li /ul h3Who You Are /h3 ul liBachelor's degree in Health Sciences (Pharmacy, Biology, Chemistry), with a Master's or Postgraduate degree in the pharmaceutical sector and/or Pharmacovigilance, Bioinformatics, Biostatistics, or Data Analytics considered an asset. /li li1–2 years of experience in a similar position within the pharmaceutical industry (CRO or pharmaceutical company). /li liExperience with Excel, Excel Macros, SQL, Business Objects, RStudio, Data Analytics, or Business Intelligence tools is highly valued. /li liKnowledge of E2B(R2), E2B(R3), MedDRA, WHO Drug Dictionary, and medical terminology is considered an advantage. /li liAdvanced level of English. /li /ul h3What We Offer /h3 pIt is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment. /p pGrifols is an equal opportunity employer. /p h3Flexibility for U Program /h3 pHybrid Model. /p h3Benefits Package /h3 h3Contract of Employment /h3 pPermanent position. /p h3Location /h3 pSant Cugat del Vallès, Spain. /p pFor more information, visit /p /p #J-18808-Ljbffr

pGaming Laboratories International (GLI) seeks a Document Specialist I to support the QA team in Spain, reviewing engineering files for regulatory compliance and compiling certification documents. The role focuses on LATAM Spanish and English, with the ability to read, write, and research across jurisdictions. /ppKey duties include reviewing documentation, maintaining certification processes, and using Protrack to manage QA reports. /p #J-18808-Ljbffr

ppAt Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. /ppThe Position Are you passionate about driving scientific strategies that transform clinical practice and improve patients' lives? We are looking for a Medical Affairs Lead to define and execute the comprehensive medical strategy for Roche Diagnostics Spain. In this high-impact role, you will serve as the primary liaison between the scientific community, international expert networks, and Roche’s global medical teams. Your mission will be to lead evidence generation, shape the scientific positioning of our diagnostic solutions, and act as a key internal strategic partner—ensuring that science and clinical excellence guide our business decisions. /ph3Your Main Responsibilities /h3ulliIntegrated Medical Strategy Leadership: Develop and execute integrated medical plans across key therapeutic areas, aligning local priorities in Spain with Roche’s global medical strategy. /liliKOL Engagement Scientific Partnerships: Lead engagement with a broad national network of Key Opinion Leaders (KOLs) and Tier-1 international experts. You will foster long-term scientific partnerships and capture high-quality clinical insights to inform strategic decision-making. /liliEvidence Generation Early Adoption: Drive the generation of required medical evidence (both company-sponsored and Investigator-Initiated Studies) in alignment with strategic priorities, enabling the early adoption of Roche’s technologies into clinical practice guidelines and consensus statements. /liliMedical Education Capability Building: Design and deliver medical education and training programs for field teams, enhancing scientific communication, technical accuracy, and engagement effectiveness. /liliCross-Functional Strategic Partnership: Provide scientific leadership and influence decision-making across internal stakeholders (Marketing, Market Access, Sales, and Medical), ensuring accuracy, regulatory compliance, and alignment with the overall medical strategy. /li /ulh3Who You Are /h3pWe are looking for a candidate with a strong scientific background, business acumen, and proven leadership through influence. /ph3Education /h3pDegree in Life Sciences (MD, MSc, PhD). /ph3Professional Experience /h3p2 to 5 years of experience in evidence generation and project management within the healthcare sector (Medtech, IVD, or Pharma). /ph3Capabilities Core Skills /h3ulliStrategic Mindset: Ability to translate complex scientific data into actionable value propositions. /liliLeadership Drive: Results-oriented with a strong commitment to operational excellence. /liliEffective Assertive Communication: Skilled in tailoring complex technical messages for diverse audiences—from scientific boards to senior management. /liliCollaboration Teamwork: Strong interpersonal skills for cross-functional collaboration within a matrix organization. /li /ulh3Languages /h3pHigh level of English and Spanish (essential for daily interaction with global medical teams and international networks). /ph3Location /h3pSant Cugat, Barcelona. /ph3What is here for You? /h3ulliReal Impact on Healthcare: A high-visibility role where your strategic input and evidence generation projects directly contribute to transforming diagnostic solutions and personalized healthcare. /liliGlobal Exposure: Direct collaboration with global leadership teams, cross-border projects and international expert panels. /liliCulture of Innovation Development: A dynamic, flexible, and collaborative environment that fosters continuous learning, autonomy, and professional growth. /li /ulh3Who we are /h3pA healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer. We believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future. We are passionate about transforming patients’ lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. We are proud of who we are, what we do and how we do it. We are many, working as one across functions, across companies, and across the world. We are Roche. /p /p #J-18808-Ljbffr

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. Are you passionate about driving scientific strategies that transform clinical practice and improve patients' lives? We are looking for a Medical Affairs Lead to define and execute the comprehensive medical strategy for Roche Diagnostics Spain. • Integrated Medical Strategy & Leadership: Develop and execute integrated medical plans across key therapeutic areas, aligning local priorities in Spain with Roche’s global medical strategy, • KOL Engagement & Scientific Partnerships: Lead engagement with a broad national network of Key Opinion Leaders (KOLs) and Tier-1 international experts. You will foster long-term scientific partnerships and capture high-quality clinical insights to inform strategic decision-making, • Evidence Generation & Early Adoption: Drive the generation of required medical evidence (both company-sponsored and Investigator-Initiated Studies) in alignment with strategic priorities, enabling the early adoption of Roche’s technologies into clinical practice guidelines and consensus statements, • Medical Education & Capability Building: Design and deliver medical education and training programs for field teams, enhancing scientific communication, technical accuracy, and engagement effectiveness, • Cross-Functional Strategic Partnership: Provide scientific leadership and influence decision-making across internal stakeholders (Marketing, Market Access, Sales, and Medical), ensuring accuracy, regulatory compliance, and alignment with the overall medical strategy We are looking for a candidate with a strong scientific background, business acumen, and proven leadership through influence. • Education: Degree in Life Sciences (MD, MSc, PhD), • Professional Experience: 2 to 5 years of experience in evidence generation and project management within the healthcare sector (Medtech, IVD, or Pharma), • Capabilities & Core Skills:, • Strategic Mindset: Ability to translate complex scientific data into actionable value propositions, • Leadership & Drive: Results-oriented with a strong commitment to operational excellence, • Effective & Assertive Communication: Skilled in tailoring complex technical messages for diverse audiences—from scientific boards to senior management, • Collaboration & Teamwork: Strong interpersonal skills for cross-functional collaboration within a matrix organization, • Languages: High level of English and Spanish (essential for daily interaction with global medical teams and international networks), • Location: Sant Cugat, Barcelona, • Real Impact on Healthcare: A high-visibility role where your strategic input and evidence generation projects directly contribute to transforming diagnostic solutions and personalized healthcare, • Global Exposure: Direct collaboration with global leadership teams, cross-border projects, and international expert panels, • Culture of Innovation & Development: A dynamic, flexible, and collaborative environment that fosters continuous learning, autonomy, and professional growth A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer. #J-18808-Ljbffr

ph3La position /h3 pAbout Our Team /p pWe at Global Diagnostics Procurement (DOP) are a team of about 200 enthusiastic professionals, committed to driving value with our suppliers worldwide. From locations around the world and with a diverse and multicultural team, we source, manage our supplier base, develop execute category strategies and constantly develop digitize processes that enable us to best support our business to grow sustainably. If you aspire to make an impact and want to be part of a high performing and world-class Procurement team, this is for you. We are DOP. At Roche, we do now what patients need next. /p h3The Opportunity /h3 pAre you ready to optimize the sourcing operations for the advanced sensor technologies and external manufacturing networks that make near-patient testing possible? As our Sourcing Manager in Sant Cugat, Spain, you will execute end-to-end tactical procurement within our Near Patient Care (NPC), Sensors Cartridges, and External Manufacturing (EM) portfolios. In this role, you will elevate standard transactional requests into strategic, value‑add opportunities, drive bottom‑line cost savings, and ensure global supply reliability. /p ul liReporting Line: The position directly reports to the Sourcing Lead – NPC, Sensors Cartridges, and EM, and is part of the Procurement Center of Excellence (CoE). /li liWider team and stakeholders: Partners with DOP Category, DOP Delivery, RSS Demand to Pay, global operations stakeholders, and external suppliers/contract manufacturers to resolve administrative bottlenecks and inform future strategies. /li liRole Type: An Individual Contributor role focused on end‑to‑end sourcing execution, master data management, and value creation. /li liImpact: You drive global procurement efficiency, value execution, and compliance across your portfolios. Specifically, you are accountable for: ul liSourcing Execution: Executing global sourcing activities, standard processes (RfIs, RfQs, RfPs), and market benchmarking for on‑market products and New Product Introductions (NPI). /li liDemand Aggregation: Analyzing user requirements to identify value‑driving methods, aggregating global demand to maximize leverage, and escalating non‑standard requests to Category Management. /li liProject Risk Management: Developing comprehensive project plans (timelines, milestones, resources), participating in project teams, and proactively identifying and mitigating risks to objectives. /li liContract Lifecycle: Setting up template‑based contracts (such as CDAs and SOWs) and managing their full lifecycle, repository tracking, and potential renewals or improvements. /li liOperational Excellence: Utilizing enterprise tools (SAP, myBuy) to simplify new and existing workflows, managing purchasing documentation, and ensuring strict compliance with global procurement policies. /li liMetrics CSR: Tracking and delivering on key operational targets and customer service metrics (such as cycle times) while championing supplier diversity, sustainability, and ethical practices. /li liConflict Exposure: Managing process expectations and competing activity priorities, while presenting regular KPI and project updates to the Sourcing Lead and global stakeholders. /li /ul /li /ul h3Who you are /h3 ul liEducation: A University degree (Business or Life Sciences preferred) is required; an MBA or CIPS certification is highly desirable. /li liExperience: 3–5+ years in sourcing, specializing in tactical sourcing (spot buying) and contract management, with a proven track record of driving cost‑reduction initiatives. /li liMarket Expertise: Relevant procurement experience within direct categories in the medical device, healthcare, or high‑tech manufacturing sectors, with hands‑on knowledge or strong exposure to Near Patient Care (NPC) technology, Sensor technology, Cartridge production, or working with External Manufacturers (EM). /li liAI Digitalization: Advanced knowledge in AI application and a strong affinity to explore AI‑driven solutions broadly, particularly regarding the digital transformation of operations (Digital 2.0 / Industry 4.0). /li liSystems Analytics: Strong, hands‑on experience with Enterprise Systems (specifically SAP), Procure‑to‑Pay (P2P) workflows, eSourcing/eAuction platforms, and BI tools like Tableau. /li liMindset Soft Skills: An analytical problem‑solver with a strong customer‑service focus. You excel at translating complex business needs into clear, compliant procurement specifications while managing project timelines and navigating conflicting priorities. /li liLanguages: Business‑level fluency in English is required; Spanish and German language skills are a strong asset. /li /ul pbRoche est un employeur offrant l'équité en matière d'emploi. /b /p /p #J-18808-Ljbffr

Experteer Overview In this role you will lead and optimize critical development processes to ensure safe, effective products and regulatory compliance. You will work cross-functionally within the Design Control Excellence team to manage requirements, risk, configuration, defects, and Vu0026amp;V across complex projects. You will drive simplification for faster time-to-market while upholding quality. This is a hands-on, global role that shapes how we deliver patient-centered solutions at Roche. Compensaciones / Beneficios • Provide expert guidance on governance for complex system, software, and assay projects across risk, requirements, configuration, and defect management. • Support multi-level requirements traceability with a streamlined, database-driven approach. • Lead strategic product risk assessments with cross-functional teams. • Build and maintain configuration management for complex projects. • Ensure Verification u0026 Validation activities meet internal standards and global regulatory requirements (e.g., ISO 13485). • Identify opportunities to simplify processes to improve time-to-market without compromising quality. • Collaborate in a global, agile, cross-cultural environment to deliver results for patients. Responsabilidades • Master’s degree in Engineering, Life Sciences, Natural Sciences, or a related field. • Minimum of three years’ experience in a regulated environment within product development or process management. • Strong understanding of Design Control processes and global standards such as ISO 13485 or IEC 62304. • Digital fluency with ALM tools (e.g., Jira, Azure DevOps) and specialized requirements management software. • Excellent English communication skills for collaboration across international sites. Requisitos principales •

Senior Business Product Owner AI & Knowledge Management ¿Todo listo para enviar su solicitud? Por favor, lea la descripción al menos una vez antes de hacer clic en "Solicitar". The Senior Business Product Owner (Sr BPO) delivers scalable, high-impact solutions and automated processes for global customer service. The Sr BPO steers agile teams, aligns stakeholders, and drives adoption to deliver business value. As Sr BPO AI & Knowledge Management you are responsible for advanced Service Knowledge Management solutions, centered around AI and AI‑ready data pipelines. This role requires a blend of technological expertise and functional judgment to meet quality goals and the service community’s needs. Field experience in the Roche Diagnostics service business, or a comparable environment, is a major plus. Your Key Responsibilities • Product Strategy & Roadmap: Own the end-to‑end product vision, translating field‑user needs and business priorities into a strategic digital roadmap, • Process Optimization & Automation: Architect scalable global use cases and identify automation opportunities to streamline technical service operations, • Data Strategy: Shape the information architecture in collaboration with IT and subject matter experts, ensuring fitness for purpose and interoperability. Ensure data compliance, design platform‑specific governance, and align with overarching standards., • Lifecycle & Delivery Management: Manage the complete product lifecycle from concept to deployment, ensuring on‑time delivery while managing cross‑program dependencies and risks, • Agile Team Leadership: Guide, mentor, and align multiple agile squads – including IT Solution Owners, Product Designers, and developers – toward successful delivery, • Stakeholder & IT Collaboration: Partner with senior business leaders to align product strategies with corporate goals, and collaborate with IT/Architecture teams to ensure technical scalability Who you are • Master’s degree in STEM or Economics / Business Administration, or equivalent experience; exhibiting excellence and fluidity on the intersection of business and technology. 5‑10 years work experience in a high‑tech, engineering, or service‑oriented business, • Technical Service Domain: Understanding of global field operations and service workflows is a distinct advantage, • AI & Tech Stack Savvy with a User Focus: Combine a confident understanding of LLMs and their surrounding tech stack (e.g. RAG architectures, prompt engineering, vector databases, and AI‑ready data pipelines) with a strong capacity for the functional, content‑driven dimension, effectively translating technical capabilities into high‑impact solutions for the service user community., • Product Lifecycle Ownership: Expert at architecting scalable global workflows and driving digital automation, with end‑to‑end delivery of solutions from concept to global rollout and user adoption, • Agile Team Steering: Proven experience leading and aligning multiple cross‑functional agile squads, • Stakeholder Alignment: Strong ability to bridge the gap between senior business executives and IT/Architecture teams. Skilled at building data‑driven business cases, defining KPIs, and maximizing product ROI This is a unique opportunity to shape the future of AI‑powered service intelligence at Roche Diagnostics. If you are passionate about technology‑driven business transformation, we’d love to hear from you! Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Sant Cugat del Vallès. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process. xkdbapo Roche is an Equal Opportunity Employer. #J-18808-Ljbffr

ph3Position Title /h3 pSecurity Affiliate Manager EMEA-LATAM /p h3About the Role /h3 pThe Security Affiliate Manager EMEA-LATAM will support affiliates with their product security needs by designing, coordinating, and governing a security network across our affiliates. /p pWe look for someone with expertise in product security and direct experience working with customers in that field. /p h3Your Responsibilities /h3 ul liBe an ambassador and evangelist for Roche Diagnostics product security to affiliates. /li liDevelop strong working relationships with key stakeholders within the regions and around the global organization. /li liDesign, coordinate, and govern a product security network across our affiliates consisting of colleagues who interface with customers on product security topics. /li liGather intake from affiliates on customer needs and expectations (e.g., data localization, support topics, etc.) to drive global product security privacy strategy improvements. /li liSupport affiliates with their product security needs, e.g., hosting training sessions, QA's, and other materials to meet customer needs; join affiliates for customer meetings, etc. /li liMake relevant product security information on products, services and ecosystem accessible to affiliates. /li liBuild the bridge between affiliate and global teams, e.g., by facilitating knowledge sharing between those (within PSPO, product teams, etc.), leading cross‑functional projects to establish processes, drive implementation of product security changes, etc. /li liCreate and maintain a knowledge base of the most common product security questions to allow affiliates to respond faster to tenders/questionnaires. /li liGather product security‑related metrics and provide report‑outs to affiliates and management. /li liCollaborate within the chapter and other PSPO chapters to ensure affiliate needs are tracked and served; be a reference for stakeholders and actively share ideas and expertise, leading or moderating discussions. /li liEnable affiliate leaders and customer‑facing roles including commercial and service to achieve greater promotion on topics of security with customers. /li /ul h3Your Experience Skills /h3 ul liBA/BS in Information Systems, Computer Science, or relevant area of study, required. /li liExpertise in working directly with customers in the product security field is required. /li liCommercial mindset. /li liFluent in English on a business level with excellent verbal and written skills; other languages welcome, but not required. /li liDemonstrated proficiency in communicating security and privacy strategy, products, and ecosystems. /li liExceptional demonstration, presentation, and interpersonal communication (written and verbal) skills are essential. /li liHighly influential relationship builder. /li liExperience with compliance standards and regulatory mandates, security and privacy laws, regulations and standards. /li liGoal‑oriented individual, with proven positive leading in the matrix ability, strong business acumen, strong focus motivating and developing teams. /li liEU residence/citizenship preferred. /li /ul h3Equal Opportunity Statement /h3 pRoche is an Equal Opportunity Employer. /p /p #J-18808-Ljbffr

ppbBuscamos especialistas hipotecarios para equipo comercial. /b /p p¿Tienes experiencia en bhipotecas, intermediación financiera o asesoramiento hipotecario /b y buscas un proyecto donde crecer profesionalmente? /p pEstamos incorporando btalento especializado /b para bdesarrollar cartera propia /b, asesorar a clientes y, si lo deseas, bliderar tu propio equipo /b dentro de un proyecto en expansión. /p h3A quién buscamos /h3 pProfesionales con experiencia en el sector hipotecario, financiero o inmobiliario, con clara orientación al cliente y a resultados, capaces de ofrecer un acompañamiento experto en todo el proceso de financiación. /p pPersonas con iniciativa, ambición y ganas de impulsar su carrera, con la opción de desarrollar un bproyecto de liderazgo /b. /p ul libAltos incentivos sin límite /b ligados a producción /li libFlexibilidad y autonomía real /b para organizar tu actividad /li libFormación continua /b, certificaciones y actualización regulatoria (LCCI, compliance, normativa bancaria) /li libSoporte comercial, marketing digital y herramientas de captación /b /li libAcompañamiento y plan de carrera /b, con posibilidad de escalar a puestos de coordinación y dirección /li liAcceso a bacuerdos con entidades financieras /b /li liCartera ampliada con productos complementarios: reunificación, ampliación de capital, seguros vinculados y soluciones de protección... /li /ul /p #J-18808-Ljbffr

ppAt Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. /p h3The Position /h3 pEstamos comprometidos no sólo con el avance de soluciones diagnósticas que puedan ayudar a los profesionales sanitarios a tomar decisiones críticas para la salud de sus pacientes, sino también con la mejora de la forma en que estas herramientas esenciales se integran en los sistemas sanitarios de todo el mundo, a un coste menor, sin dejar de obtener los mejores resultados posibles. /p pEn más de 100 países, ofrecemos la cartera de pruebas de diagnóstico in vitro más completa del sector, combinada con apoyo a la toma de decisiones clínicas, consultoría, diagnóstico digital, gestión de enfermedades, automatización de laboratorios y soluciones de software para proporcionar soluciones integradas a laboratorios, clínicos y sistemas sanitarios. /p h3What is your Mission? /h3 pYou will be the key operational engine within Roche Diagnostics Spain (RDE), reporting directly to the leadership team. Your main mission is to ensure business agility and efficiency, freeing up high-value time for our strategic and customer-facing teams. /p pYou will combine excellence in administrative management with innovation, optimizing processes through the implementation of Artificial Intelligence and ensuring regulatory compliance at a national level. If you are passionate about efficiency, technology, and strategic impact, this is your place. /p h3Your Key Responsibilities /h3 ul liExecutive Management and Agile Coordination: Administer and coordinate complex agendas, plan travel, and organize key events for leadership and commercial teams, always prioritizing direct business impact /li liStrategic External and Internal Articulation: Facilitate and coordinate the leaders' interaction with strategic external and internal partners to drive commercial success, strategic initiatives, and cross-functional projects in our commercial headquarters /li liCommercial Strategic Support: Provide direct support to key account teams, including preparing client briefings, managing data in the CRM system, and administrative follow‑up on executive actions /li liPioneer in AI and Automation: Proactively identify repetitive tasks in various areas and design and implement automation solutions, using AI agents (such as generative models) /li liCompliance Assurance: Act as a liaison to ensure that all administrative processes strictly comply with internal policies for Finance, Human Resources, and Business Integrity /li liCross‑functional Collaboration and Support: Participate in coordinating mutual support among assistants, ensuring service continuity and a balanced workload across the organization /li /ul h3What We Look for in You /h3 ul liEducation: Professional degree or equivalent. Training in project management will be especially valued /li liExperience: Minimum of 5 years of demonstrable experience in executive support roles, team coordination, or administrative management in large‑scale corporate environments (ideally in matrix or network structures) /li liLanguages: Fluent command (oral and written) of English and Spanish (essential) /li liDigital and Technological Experience and Mindset: Advanced user of cloud ecosystems (Microsoft 365/Google Workspace) and a proactive, demonstrable curiosity for the application of Generative Artificial Intelligence /li /ul h3Competency /h3 ul liBusiness and Operation Skills /li liProcess Architecture: Ability to analyze a complex activity and break it down into logical, efficient, and automatable flows /li liPrompt Engineering: Practical ability to interact with AI tools (e.g., ChatGPT, Copilot) for content generation, summarization, and data analysis /li liProject Management: Familiarity with and mastery of agile methodologies (e.g., Kanban) and project management tools (e.g., Trello, Monday, Planner) /li liData Literacy: Ability to interpret dashboards and ensure data quality and hygiene in systems /li liLeadership and Impact /li liStrategic Thinking: Capacity for systemic thinking, understanding the overall impact of decisions and consistently prioritizing long‑term and organizational benefits over short‑term gains /li liInfluence and Vision: You will be a role model, with a Visionary, Architect, and Catalyst mindset, capable of inspiring and aligning stakeholders /li liInterpersonal Skills and Resilience /li liEmpathic Communication: Excellent active listening skills to understand and empathize with diverse internal and external stakeholders /li liConflict Management: Comfort in constructively expressing and debating different opinions, seeking to generate better results and innovative solutions /li liCultural Agility: Demonstrated ability to navigate and adapt to difficult or complex situations, maintaining calm and focus, and having lived or worked in culturally diverse environments /li liDisruption and Innovation: Ability to embrace the unexpected and foster disruptive thinking in the search for solutions /li /ul h3Who we are /h3 pA healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life‑changing healthcare solutions that make a global impact. /p pLet’s build a healthier future, together. /p pbRoche is an Equal Opportunity Employer. /b /p /p #J-18808-Ljbffr

ppChez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement. Voici comment nous visons à prévenir, arrêter et guérir les maladies et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Rejoignez Roche, où chaque voix compte. /p h3La position /h3 pAbout Our Team /p pWe at Global Diagnostics Procurement (DOP) are a team of about 200 enthusiastic professionals, committed to driving value with our suppliers worldwide. From locations around the world and with a diverse and multicultural team, we source, manage our supplier base, develop execute category strategies and constantly develop digitize processes that enable us to best support our business to grow sustainably. If you aspire to make an impact and want to be part of a high performing and world-class Procurement team, this is for you. /p pWe are DOP. At Roche, we do now what patients need next. /p h3The Opportunity /h3 pAre you ready to shape the long-term supplier strategies and project pipelines that deliver medical innovation to patients worldwide? As our Associate Category Manager (ACM) in Sant Cugat, Spain, you will support the development, validation, and execution of global category strategies and annual strategic initiatives. In this role, you will leverage rigorous procurement analytics to transform market intelligence into actionable category guidance, ensuring global supply resilience and portfolio value. /p pWe are looking to fulfill one Associate Category Manager position per team. Successful candidates will be aligned to support one of the following dedicated procurement categories: Biologicals Chemicals, Plastics Packaging, Electronics Systems, Mechanicals, Logistics. /p ul libReporting Line: /b Directly reports to the respective Category Lead within the Category organization. /li libWider Team and Stakeholders: /b Collaborates closely with Category Managers, Sourcing Managers, Delivery Managers, Finance, Legal, and external market intelligence providers. Participates in a global ACM Community of Practice (CoP) coordinated by the Category Integration Excellence Lead to ensure consistency of methodologies, reporting standards, strategic planning processes, and cross-category collaboration. /li libRole Type: /b An Individual Contributor role in support of the allocated Category, focused on strategic enablement, market data intelligence, and stakeholder management. /li libImpact: /b You drive category compliance, data integrity, and strategic execution across the global operations network. Specifically, you are accountable for: /li ul liStrategy Pipeline Support: Collation of supplier, market, and internal business data to help formulate the long-term Category Strategy and build a proactive pipeline of future initiatives. /li liStrategic Initiative Deployment: Supporting Category Managers, Project Delivery, Delivery, and Sourcing Managers in executing and deploying complex projects in strict compliance with global standards and procedures. /li liNegotiation Contracting Preparation: Supporting contract drafting and vendor negotiations for strategic, key, or bottleneck suppliers by delivering comprehensive analytics, fact‑bases, and market benchmarks. /li liStrategic Sourcing: Support selected high‑value strategic sourcing initiatives and complex RFx activities to convert pipeline targets into realized business value. /li liReporting Analytics: Collaborating with data analytics experts to generate Category‑specific insights, generating monthly spend/savings metrics, and conducting data validation to safeguard governance. /li liImplementation Support: Converting strategic outcomes into clear category guidance documents and support materials to ensure category strategies can be effectively implemented across the organization. /li /ul /ul h3Who you are /h3 pWe look for analytical problem‑solvers with excellent interpersonal competencies who can seamlessly guide stakeholders through complex procurement processes. /p ul libEducation: /b University degree (Business or Life Sciences focus preferred). Professional purchasing (e.g., CIPS), project management (e.g., PMP, Prince 2), or Finance‑related licenses are highly advantageous. /li libExperience: /b 2+ years of procurement or supply chain experience focused on strategic sourcing, enterprise cost reduction, or operational efficiency initiatives. /li libMarket Knowledge: /b Demonstrated understanding of major direct spend categories, spend levers, and supply market fundamentals. /li libSystems Analytics: /b Strong experience driving insights from large data sets, utilizing data visualization applications (specifically Tableau and ThoughtSpot), enterprise systems (SAP/Oracle), and eSourcing/eAuction platforms. /li libAI Digitalization: /b Advanced knowledge in AI application and a strong affinity to explore AI‑driven solutions broadly, particularly regarding the digital transformation of operations (Digital 2.0 / Industry 4.0). /li libMindset Soft Skills: /b A strong communicator capable of effective upwards management and conflict resolution. You possess the ability to translate messy data into clear procurement specifications with a proactive, customer‑centric focus. /li libOperating Principles: /b Driven to live the Roche Operating Principles daily - simplifying radically, acting as one team, thinking long‑term, and prioritizing patient outcomes above all else. /li libTravel: /b Ability to travel domestically and internationally up to 10% of the time for supplier and internal network meetings. /li /ul pbRoche est un employeur offrant l'équité en matière d'emploi. /b /p /p #J-18808-Ljbffr

pK-LAGAN is seeking a Quality Engineer for a technical project in Terrassa, Spain, focused on product quality in the automotive sector. The role requires hands-on experience in validation and development of mechanical components and is ideal for candidates with a degree in Engineering and 2-3 years of experience. /ppKey responsibilities include leading FMEA activities, ensuring compliance with quality requirements, and collaborating with engineering teams. The position offers a permanent contract, opportunities for career development, and various social benefits. /p #J-18808-Ljbffr

ph3The Opportunity /h3pAs our Business Capability Lead (BCL) located in Sant Cugat, Spain, you will take strategic and operational ownership over critical segments of the global Demand-to-Pay process landscape. In this high‑impact role, you will define process governance, integrate complex interfaces across corporate ecosystems, and serve as a vital change agent to accelerate the myBuy solution adoption across the enterprise. /ph3Reporting Line /h3pReports directly to the Sourcing Lead and is part of the Procurement Center of Excellence (CoE). Leads a global Business Capability Community formed by SMEs. Manages cross‑functional relationships across the DOP Leadership Team, CoE LT, DOP Delivery, DOP Sourcing Teams, RSS Demand to Pay, Global Procurement, and external technology providers. /ph3Impact /h3pDrive global operational efficiency, process compliance, and large‑scale digital adoption. Specifically, you are accountable for: /ph3Responsibilities /h3ullibProcess Design Strategy: /b Developing and deploying the DOP roadmap for myBuy, in alignment with functional partners like DIA Global Supply Chain and RSS Demand to Pay. /lilibAutomation Innovation: /b Proactively identifying opportunities for process automation and digitalisation in close collaboration with Delivery, Category, Digital Process Management, and RSS Demand to Pay. /lilibSME Analysis Governance: /b Acting as a deep subject matter expert to analyse, elaborate options, and design solutions that resolve process, system, performance indicator, or data concerns, while supporting data and rule definitions. /lilibTransformation Project Delegation: /b Serving as a responsible delegate on major corporate initiatives (such as the ASPIRE program) to support global template adoption and evaluate localised change impacts. /lilibContinuous Improvement: /b Leading continuous improvement initiatives, managing global requirement alignment, and partnering with fellow BCLs and Business Capability Owners to optimise end‑to‑end cross‑functional performance. /lilibCommunity ARTS Representation: /b Leading the Business Capability Community of SMEs and representing DOP in communities and Agile Release Trains (ARTs). /lilibKnowledge Management: /b Governing the development, structural maintenance, and delivery of global system process documentation and training materials. /lilibConflict Exposure: /b Resolving matrix conflicts regarding competing project priorities or process expectations, while delivering high‑frequency monthly or quarterly KPI updates to the CoE LT and DPLT. /li /ulh3Qualifications /h3ullibEducation: /b University degree with a business or life sciences focus is required; a Master's degree (MBA or equivalent) and professional certifications (such as CIPS) are highly preferred. /lilibExperience: /b Deep expert knowledge of procurement systems and enterprise architectures (e.g., SAP S/4HANA, GEP Smart / GEP Nexxe), coupled with a robust understanding of the broader procurement technology provider landscape. /lilibProcess Expertise: /b Extensive experience in the design, management, and continuous improvement of complex business processes, with distinct experience operating within the Demand‑to‑Pay landscape. /lilibAI Digitalisation: /b Advanced knowledge in AI application and a strong affinity to explore AI‑driven solutions broadly, particularly regarding the digital transformation of operations. /lilibChange Stakeholder Management: /b Proven track record of guiding stakeholder groups, managing escalations, navigating communication lines, and leading cross‑functional project teams without direct headcount authority. /lilibMindset Soft Skills: /b Self‑organised, motivated professional with a solution‑oriented "Can-Do" attitude and an end‑to‑end business perspective. Excellent negotiation and conflict resolution skills, acting as a customer‑oriented partner who champions an open speak‑up and error culture. /lilibLanguages: /b Business‑level fluency in English is required; German language skills are a strong asset. /li /ulpRoche is an Equal Opportunity Employer. /p /p #J-18808-Ljbffr

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position About Our Team We at Global Diagnostics Procurement (DOP) are a team of about 200 enthusiastic professionals, committed to driving value with our suppliers worldwide. From locations around the world and with a diverse and multicultural team, we source, manage our supplier base, develop & execute category strategies and constantly develop & digitize processes that enable us to best support our business to grow sustainably. If you aspire to make an impact and want to be part of a high performing and world-class Procurement team, this is for you. We are DOP. At Roche, we do now what patients need next. The Opportunity Are you ready to shape the long-term supplier strategies and project pipelines that deliver medical innovation to patients worldwide? As our Associate Category Manager (ACM) in Sant Cugat, Spain, you will support the development, validation, and execution of global category strategies and annual strategic initiatives. In this role, you will leverage rigorous procurement analytics to transform market intelligence into actionable category guidance, ensuring global supply resilience and portfolio value. We are looking to fulfill one Associate Category Manager position per team. Successful candidates will be aligned to support one of the following dedicated procurement categories: Biologicals & Chemicals, Plastics & Packaging, Electronics & Systems, Mechanicals, Logistics. - Reporting Line: Directly reports to the respective Category Lead within the Category organization. - Wider Team and Stakeholders: Collaborates closely with Category Managers, Sourcing Managers, Delivery Managers, Finance, Legal, and external market intelligence providers. Participates in a global ACM Community of Practice (CoP) coordinated by the Category Integration & Excellence Lead to ensure consistency of methodologies, reporting standards, strategic planning processes, and cross-category collaboration. - Role Type: An Individual Contributor role in support of the allocated Category, focused on strategic enablement, market data intelligence, and stakeholder management. - Impact: You drive category compliance, data integrity, and strategic execution across the global operations network. Specifically, you are accountable for: - Strategy & Pipeline Support: Collation of supplier, market, and internal business data to help formulate the long-term Category Strategy and build a proactive pipeline of future initiatives. - Strategic Initiative Deployment: Supporting Category Managers, Project Delivery, Delivery, and Sourcing Managers in executing and deploying complex projects in strict compliance with global standards and procedures. - Negotiation & Contracting Preparation: Supporting contract drafting and vendor negotiations for strategic, key, or bottleneck suppliers by delivering comprehensive analytics, fact-bases, and market benchmarks. - Strategic Sourcing: Support selected high-value strategic sourcing initiatives and complex RFx activities to convert pipeline targets into realized business value. - Reporting & Analytics: Collaborating with data analytics experts to generate Category-specific insights, generating monthly spend/savings metrics, and conducting data validation to safeguard governance. - Implementation Support: Converting strategic outcomes into clear category guidance documents and support materials to ensure category strategies can be effectively implemented across the organization. Who you are We look for analytical problem-solvers with excellent interpersonal competencies who can seamlessly guide stakeholders through complex procurement processes. - Education: University degree (Business or Life Sciences focus preferred). Professional purchasing (e.g., CIPS), project management (e.g., PMP, Prince 2), or Finance-related licenses are highly advantageous. - Experience: 2+ years of procurement or supply chain experience focused on strategic sourcing, enterprise cost reduction, or operational efficiency initiatives. - Market Knowledge: Demonstrated understanding of major direct spend categories, spend levers, and supply market fundamentals. - Systems & Analytics: Strong experience driving insights from large data sets, utilizing data visualization applications (specifically Tableau and ThoughtSpot ), enterprise systems (SAP/Oracle), and eSourcing/eAuction platforms. - AI & Digitalization: Advanced knowledge in AI application and a strong affinity to explore AI-driven solutions broadly, particularly regarding the digital transformation of operations (Digital 2.0 / Industry 4.0). - Mindset & Soft Skills: A strong communicator capable of effective upwards management and conflict resolution. You possess the ability to translate messy data into clear procurement specifications with a proactive, customer-centric focus. - Operating Principles: Driven to live the Roche Operating Principles daily - simplifying radically, acting as one team, thinking long-term, and prioritizing patient outcomes above all else. - Travel: Ability to travel domestically and internationally up to 10% of the time for supplier and internal network meetings. Ready for the next step? We look forward to hearing from you. Apply now to discover this exciting opportunity! Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position At Roche, we believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future. We are passionate about transforming patients’ lives and we are brave in both decision and action. And we believe that good business means a better world. Join Our Team: Make a Difference in International Regulatory Affairs! Roche is seeking a dynamic and highly motivated individual to join our team as an International Regulatory Affairs Professional. We are looking for candidates who bring an innovative and creative mindset to the table, along with a proven track record in the Regulatory Affairs field. If you are passionate about making a positive impact on global healthcare through regulatory excellence, we invite you to be part of our dedicated team. Key Responsibilities As an International Regulatory Affairs Professional at Roche, you will be responsible for: - Leading and supporting regulatory strategies for global IVD/MD instruments and software submissions - Ensuring compliance with international regulatory requirements and standards - Collaborating with cross-functional teams, including R&D, Quality, and Clinical, to drive regulatory initiatives - Providing regulatory guidance to support product development and lifecycle management - Staying abreast of evolving regulatory trends and up‐ dates, and implementing best practices Requirements - Bachelor’s Degree in Life Sciences, Regulatory Affairs, or a related field - 5 to 7 years of experience in Regulatory Affairs ( Regulatory, R&D, Quality and/or Clinical), with some experience in healthcare regulatory affairs - In-depth knowledge of global regulatory requirements, guidelines, and procedures especially for IVD instruments & software - Strong organizational and communication skills - Ability to multitask and effectively manage multiple projects simultaneously - Self-motivated and capable of working independently in a self-management environment - Experience in IVD instrument and/or software development Why Roche - Collaborative and innovative work environment - Opportunity to make a meaningful impact on patients' lives globally - Competitive compensation and benefits package - Professional development and growth opportunities within a leading global healthcare organization If you are a dedicated professional who thrives in a fast-paced environment and is passionate about contributing to the International Regulatory Affairs landscape, we want to hear from you! Submit your resume and cover letter detailing your relevant experience and qualifications. Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position The Opportunity The Digital Innovation and Operational Services Chapter is a global team in R&D that focuses on internal improvement: increasing productivity, efficiency, and the ability of the R&D organization to collaborate across its global organizational interfaces. Our work involves reducing complexity of our systems, harmonizing processes, tools, and business practices, and building connections across geographical and organizational silos. We are seeking a R&D Enterprise Tools Operations Specialist to join our global support team. You are well organized and detail-oriented. You will be the reliable service provider handling critical system requests within our core business tools, ensuring our scientists and engineers worldwide can focus on developing innovative products for patients. This role requires building organizational know-how—understanding who our internal customers are, how they work, and solving problems in a way that anticipates their support needs. You are quick in learning new software systems and tools, enjoy helping your coworkers every day, and are motivated to innovate internal processes to automate tasks, you will fit right into our team! Key Responsibilities As a part of a global centralized expert support team, execute enterprise tool system tasks based on R&D customer requests, leveraging expert knowledge of business tools, compliance requirements, and R&D teams and processes. - Execute R&D System Requests: Fulfill customer tool requests using expertise in business systems and compliance standards. - Provide Timely Expert Support: Offer professional, empathetic, and quick solutions to R&D operational issues and system problems. - Expert in our Global Business Applications: Act as the subject matter expert for one or more complex R&D business applications. - Specialize in R&D Processes: Develop deep expertise in key processes (e.g., records management, lab data, change requests) for high-accuracy execution. - Maximize Scientist Productivity: Use your expertise across business data and organizational structure to streamline operations and save significant time for R&D scientists. - Anticipate Customer Needs: Build organizational know-how of R&D roles and priorities to deliver proactive system support. - Maintain Global Service Excellence: Demonstrate a strong, collaborative customer service mindset within a diverse, global team. - Drive Process Improvement: Identify manual steps and actively suggest opportunities for digitization and improvement. - Automate Administrative Tasks: Apply or develop automation and AI tools to reduce administrative load on R&D staff. - Ensure Data Integrity and Compliance: Guarantee all activities strictly adhere to regulated R&D processes, supporting audits and data retrieval. Requirements: - Education: Bachelor’s degree, preferably in a technical, scientific, or business discipline. - Experience: 2+ years of professional experience in an operations, technical support, or system administration role, or equivalent academic projects / internships - Language Skills: Excellent written and verbal English Language skills are required to support our global organization. German language skills are a plus. - System Proficiency: Ability to quickly learn new software, systems, and processes is essential. - - Prior experience in enterprise business applications is desirable (e.g., Electronic Document Management Systems, Learning Management Systems, or Project Management tools). - Education and experience in data structures, databases, automation, scripting, AI prompt engineering and/or development of AI agents is desirable - Tools : Experience with SAP, Cornerstone, Google Suite and Office Suite is a plus. - Execution & Focus: A proven ability to complete complex, detailed tasks accurately and efficiently. You have a rigorous and detail-oriented approach to following established processes. - People Skills: Demonstrated ability to work well with others in a hybrid virtual and global team environment Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer.

ppToyota Automated Logistics is a global company specializing in the design, development, and implementation of advanced intralogistics automation solutions. Through cutting‑edge technology and strong engineering expertise, the company optimizes internal material flows, enhancing operational efficiency, safety, and sustainability across industrial environments, in line with the principles of the Toyota Production System. /ph3Your impact /h3pThe HR Generalist plays a key role in the execution and coordination of core Human Resources activities, ensuring efficient, compliant, and people‑focused HR operations. Reporting to the HR Director, the role supports the full employee lifecycle with a strong emphasis on execution, process excellence, and alignment with company policies and business needs. The HR Generalist acts as a trusted point of contact for employees and managers, contributing to a consistent and professional HR service across the organization. /ph3Skills /h3ulliStrong interpersonal and communication skills, with the ability to interact effectively at all organizational levels. /liliHigh level of integrity, discretion, and professionalism when handling confidential information. /liliExcellent organizational and time‑management skills, with the ability to prioritize tasks in a dynamic environment. /liliProactive and solution‑oriented mindset, with strong attention to detail and execution quality. /liliAbility to work independently while collaborating effectively within cross‑functional and international teams. /liliSound judgment and emotional intelligence when addressing employee‑related matters. /liliAdaptability and resilience in a fast‑paced, evolving business environment. /liliCustomer‑oriented approach, with a strong focus on service excellence and employee experience. /li /ulh3Qualifications /h3ulliBachelor’s degree in Labor Relations, Business Administration, or a related field. /liliMinimum of 4–5 years of proven experience in Human Resources, preferably with a focus on labor relations or employment law. /liliHands‑on experience in multidisciplinary HR functions, including employee relations, HR administration, payroll support, recruitment, and performance management. /liliSolid knowledge of Spanish labor laws, HR best practices, and compliance requirements. /liliDemonstrated ability to manage HR processes end‑to‑end with accuracy and attention to detail. /liliExperience working in international or matrix organizations is a plus. /liliStrong analytical, problem‑solving, and organizational skills. /liliAdvanced English level. /li /ulh3General Duties /h3ulliRecruiting (core of the role) /liliJob postings /liliCandidate screening /liliInitial interviews /liliCoordination with managers /lili50 % travel /liliMeetings with managers /liliFollow‑up on new hires /liliResolution of local incidents /liliOperational design of onboarding programs /liliFollow‑up during the first months /liliAdministrative management of exits /liliCommunication with managers /liliVacation requests /liliSick leaves /liliMinor conflicts /liliBasic contractual questions /liliEnsure compliance with labor regulations, internal policies, and corporate HR standards. /liliAct as a first‑level contact for employee queries related to HR policies, procedures, and administrative matters. /liliSupport performance management, training coordination, and employee development initiatives from an operational perspective. /li /ulh3About Us /h3pShape the future of intelligent warehousing. At Toyota Automated Logistics (TAL), you help shape the future of intelligent warehousing. As part of Toyota Industries Corporation (TICO), we are a global partner for integrated warehouse automation. Founded in April 2026, we bring together the strengths of Bastian Solutions, Vanderlande’s Warehousing business, and viastore under one brand. Together, we form an integrated automation hub delivering scalable systems, intelligent software, and lifecycle services to customers around the world. Our ambition is clear: to set industry standards and shape the future of intralogistics. /p /p #J-18808-Ljbffr

ph3Overview /h3 p¿Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? Grifols es una compañía global del sector de la salud que desde 1909 mejora la salud y el bienestar de las personas en todo el mundo. Somos líderes en medicamentos hemoderivados y medicina transfusional y desarrollamos, producimos y comercializamos medicamentos, soluciones y servicios innovadores en más de 110 países y regiones. /p h3Mission /h3 pTo review and ensure that all procedures, testing methods and reports established in GEPD Plasma Testing Laboratories are in compliance to Egyptian regulations, and in accordance to cGMP, following Plasma Testing Specifications established and European Regulation. To manage and supervise Plasma Testing Laboratories Quality projects. To propose continuous improvement measures related to the quality systems of the Laboratories. To supervise the Quality Risk Management (QRM) process for the Laboratories. /p h3Responsibilities /h3 ul liTo review and ensure that all procedures established are in accordance to cGMP. ul liTo supervise GEPD Plasma Testing Laboratories quality system and quality culture. /li liTo ensure investigation for incidents are initiated, as well as root cause analysis are properly in place. /li liTo participate and support internal and external regulatory inspections and audits performed in the Laboratories. /li /ul /li liTo manage and supervise Plasma Testing Laboratories Quality projects. ul liActively participate in Laboratory meetings for the follow-up of activities related to open Change Controls. /li liCoordinate the tasks required to be developed within the different areas of the company. /li liReview new procedures and processes to be implemented in the Laboratory under the scope of the Change Controls open. /li /ul /li liTo ensure continuous improvement measures related to the quality systems of the Laboratories. ul liTo supervise the monitoring of corrective and/or preventive actions implemented within the Laboratories. Ensure their proper implementation and effectiveness. /li liTo monitor quality system indicators. /li liTo propose improvements in the Laboratory's processes to enhance the quality system. /li /ul /li liTo supervise the Quality Risk Management (QRM) process for the Laboratories. ul liTo supervise Quality Risk assessment studies and reports, as well as coordinate mitigation tasks. /li /ul /li /ul h3Who You Are - Qualifications /h3 ul liBachelor’s Degree in Life Sciences (Biology, Pharmacy, Biotechnology or related fields). /li liMinimum 3-5 years of experience in a related field. /li liOrganized and able to manage time effectively. /li liAbility to work within a highly regulated, labor intensive environment. /li liAbility to understand, explain, follow, and enforce SOPs. /li liAbility to plan, communicate and execute activities for the improvement of overall operations. /li liStrong integrity and commitment to Quality and Compliance. /li liExcellent oral and written communication skills to produce clear and concise factual findings. /li liAdvanced level of Spanish and English. /li liThis position requires significant travel and on-site presence in Egypt, with approximately 50% of the role based in Egypt. /li /ul h3Benefits and Location /h3 ul liContract of Employment: Permanent position. /li liLocation: Sant Cugat del Vallès, Spain. /li liFlexibility for U Program: Occasionally Remote. /li /ul h3Equal Opportunity Statement /h3 pGrifols is an equal opportunity employer. /p /p #J-18808-Ljbffr

ph3Job Summary /h3pResponsible Sourcing Program Manager – At HP, our bold ambition is to redefine the Future of Work with technology, creating experiences that drive growth and more fulfilling work experiences for people everywhere. Transforming HP's Value Chain is at the center of our sustainability strategy where we innovate for performance and resilience. /ppThis Intermediate staff level position within HP's Global Responsible Sourcing Team is responsible for drafting and maintaining policies and supplier requirements related to Responsible Sourcing, managing sustainability content in HP's supplier handbook, leading the supplier training program, and supporting strategic initiatives led by senior staff members related to supplier due diligence. The role builds and maintains relationships with internal stakeholders and champions Responsible Sourcing across all components, parts, and products HP procures. /ph3Responsibilities /h3ulliCoordinate the annual update of all policies and work with senior staff to develop new policies as needed to meet future regulations. /liliPartner with colleagues across HP's Global Product Compliance and Sustainability (GPCS) organization to maintain a current list of supplier requirements and ensure up‑to‑date requirements are reflected in HP's Supplier Handbook. /liliDevelop and implement the annual supplier training program across all HP suppliers, collaborating with colleagues on training content development and ensuring effective delivery to target audiences. /liliDrive the implementation of due diligence compliance deliverables as prescribed by senior staff to meet regulatory requirements such as the Corporate Sustainability Due Diligence Directive (CSDDD), Modern Slavery Transparency Statement, and Mitigation and Prevention of Risks to Rights Holders. /liliEstablish and maintain effective working relationships and coordinate with procurement and other stakeholders encountered in the performance of duties. /li /ulh3Education Experience Recommended /h3ulliBachelor or Master’s Degree in Human Rights, Sustainability, Supply Chain, or Engineering. /liliTypically 2–4 years of work experience, preferably in Supply Chain Environmental Social and Corporate Governance or a related field, or an advanced degree with little or no work experience. /liliFluency in English (both written and verbal). /li /ulh3Knowledge Skills /h3ulliEnvironmental Social and Corporate Governance (ESG) /liliHuman Rights /liliInternal Communications /liliProject Management /liliThought Leadership /li /ulh3Cross‑Org Skills /h3ulliEffective Communication /liliResults Orientation /liliLearning Agility /liliDigital Fluency /liliCustomer Centricity /li /ulh3Disclaimer /h3pThis job description describes the general nature and level of work performed in this role. It is not intended to be an exhaustive list of all duties, skills, responsibilities, knowledge, etc. These may be subject to change and additional functions may be assigned as needed by management. /ppEqual Opportunity Employer (EEO) – HP, Inc. provides equal employment opportunity to all employees and prospective employees, without regard to race, color, religion, sex, national origin, ancestry, citizenship, sexual orientation, age, disability, or status as a protected veteran, marital status, familial status, physical or mental disability, medical condition, pregnancy, genetic predisposition or carrier status, uniformed service status, political affiliation, or any other characteristic protected by applicable national, federal, state, and local law(s).The information obtained will be kept in strict confidence. For more information, review HP’s EEO Policy or read about your rights as an applicant under the law: Know Your Rights: Workplace Discrimination is Illegal. /p /p #J-18808-Ljbffr

Experteer Overview As a System Administrator at Kyndryl, you will tackle complex issues across diverse platforms and drive modernization for high-profile clients. You will manage client systems, ensure security compliance, and coordinate ticket queues with technicians. You’ll collaborate with cross-functional teams to identify modernization opportunities and foster strong stakeholder relationships. This role offers growth toward architectural paths, exposure to cloud hyperscalers, and a culture that values belonging and continuous learning. Compensaciones / Beneficios • Manage client systems data and provide day-to-day solutions • Ensure security compliance across platforms and services • Oversee a queue of assignments and prioritize tickets with technicians • Recommend modernization options and identify new business opportunities • Cultivate relationships with other teams and stakeholders • Collaborate with diverse teams to support clients across industries Responsabilidades • 5+ years of middleware administration • Hands-on Linux and Windows Server experience • Experience supporting business-critical production systems • Availability for out-of-hours support and on-call rotations Requisitos principales • Be Well programs: health and wellbeing • hybrid-friendly culture • learning opportunities and certifications (Microsoft, Google, Amazon) • career path and growth • coaching and hands-on experiences

ppbSener /b is currently looking for a bFabrication Manager /b for Offshore Wind Projects to join our team at our work centers in Barcelona, Madrid, Valencia or Bilbao. /p pWe are focused on engineering for the sustainability of industry and society. Therefore, we develop projects oriented towards achieving maximum efficiency in the transition towards a sustainable energy model, through innovation and technology. /p pFurthermore, we are involved in the design, development and construction of power plants and their components, covering from the most conventional technologies such as combined cycle, biomass, etc. to new renewable and future technologies such as offshore wind, green hydrogen, management, circular economy and sustainability. /p pThe Fabrication Manager provides leadership and oversight of all fabrication activities, ensuring that offshore structures are delivered safely, on time, within budget, and in accordance with contractual, technical, and quality requirements. The role interfaces daily with the contractor, supervises site teams, monitors progress, and ensures compliance with HSE, QA/QC and certification standards. /p h3What you will do: /h3 ul libLeadership Coordination /b ul liProvide leadership, direction and support in the fabrication of offshore structures. /li liEstablish and maintain strong working relationships with the Contractor at all organizational levels. /li liManage a team of supervisors and ensure effective coordination across all fabrication activities. /li liEnsure all activities are executed in line with contractual obligations, schedule, cost targets and quality objectives. /li liPromote the highest HSE standards and ensure compliance with site rules and procedures. /li /ul /li libFabrication Progress Performance Monitoring /b ul liMonitor Supplier’s progress against the overall program, milestones and KPIs, identifying risks or delays. /li liProvide regular and ad‑hoc reporting to the project leadership team. /li liIdentify risks and develop mitigation measures as part of the overall risk management process. /li /ul /li libQA/QC Documentation Management /b ul liTake proactive ownership of QA/QC topics related to fabrication. /li liSupport the closure of the EPC contract from a technical, QA/QC, HSE and commercial perspective. /li /ul /li libContractual Commercial Support /b ul liAssist in the technical analysis, monitoring and cross‑checking of variation orders and claims. /li liProvide advice on fabrication solutions, risk levels and commercial implications to ensure cost‑effective decisions. /li liEnsure all activities are aligned with delivering the works on time, within budget and to the required quality. /li /ul /li libInterface Stakeholder Coordination /b ul liManage the transition from fabrication to commissioning and/or OM, including inspections and dossier acceptance. /li /ul /li libReporting Final Deliverables /b ul liProvide progress reports in accordance with project requirements. /li liEnsure all reporting is accurate, timely and aligned with project expectations. /li /ul /li /ul h3What we expect from you: /h3 ul liBachelor or Master's Degree in Engineering or similar. /li liMinimum 10 years relevant experience in similar position. /li liProven background in fabrication oversight for one or more of the following packages: ul liOffshore Substation Topside /li liJackets /li liMonopiles /li liTransition Piece /li liWork experience as Fabrication Manager for at least one offshore wind or large‑scale oil gas project comprising from start of construction throughout equipment installation and commissioning to load out. /li liInternational Site Management experience of EPC contractors /li liProject management training /li liFIDIC Contracts and INCOTERMS /li liFabrication and testing Offshore Structures (DNV-ST-0145, DNV-OS-C401) /li liSafety Management Training for the applicable countries (NEBOSH, VCA…) /li liTraining ISO 9001, Quality Auditing or equivalent /li liExcellent written and oral English communication skills. /li liStrong communicative competence in Spanish, both oral and written, will be positively valued. /li /ul /li /ul h3What we offer: /h3 pThese are some of the benefits you will enjoy at Sener: /p ul liYou will have the opportunity to participate in innovative and high-level technological projects at an international level, collaborating with a multidisciplinary and highly qualified team. /li liYou will enjoy better management of your time thanks to our flexible working hours and remote work policies. /li liYou will be able to optimise your salary with our flexible remuneration plan (meal cards, private medical insurance, childcare vouchers, etc.) and you will have life and accident insurance. /li liWe will take care of you with our physical and emotional wellness programme, which includes sports, workshops, etc. /li liWe will encourage your professional development, with technical training, skills, languages, etc. so that you can continue to grow and achieve your goals. /li liWe promote equal opportunities, diversity and inclusion of all people and we are certified as a Family Responsible Entity (efr). /li /ul pIf you identify with our values and want to be part of a leading international family engineering company, we are waiting for you! We want to go as far as you want to go. /p /p #J-18808-Ljbffr

ppByteTravel is a TravelTech company focused on making international travel simpler through digital solutions. We provide a range of travel-related services, including visas, regulatory compliance, connectivity, mobility, and airport services for both leisure and business travelers. /ppOur products and platforms — including Visagov, Roamic, Globely, VIPLounges, and ImmiAssist — connect with travel agencies, tour operators, airlines, and cruise lines through affiliate partnerships, backend integrations, and APIs. /ppWith offices in Barcelona, Madrid, and Miami, we continue to build scalable and reliable solutions that help our partners deliver a better travel experience. /ph3About the Role /h3pWe are looking for a Chargeback Specialist to join our Operations team. In this role, you will be responsible for managing payment disputes and chargebacks, helping us minimize financial risk while ensuring a fair and efficient resolution process for our customers. /ppYou will work closely with different teams across the company, analyze dispute trends, and contribute to improving our internal processes and prevention strategies. /ph3What You'll Do /h3ulliManage the full chargeback and dispute lifecycle, from investigation and evidence gathering to response submission and follow-up. /liliReview transactions and customer cases to identify the root causes of disputes and potential fraud risks. /liliAnalyze chargeback trends and performance metrics to detect patterns and opportunities for improvement. /liliSupport the optimization of internal processes, controls, and workflows to reduce dispute volumes and improve efficiency. /liliEnsure compliance with card scheme rules, payment provider requirements, and consumer protection regulations. /liliCollaborate with Customer Support, Product, Marketing, and Legal teams to help prevent disputes before they occur. /liliMaintain accurate records and reporting related to chargeback performance, risk indicators, and operational KPIs. /liliContribute to the continuous improvement of tools, procedures, and best practices within the payment operations function. /li /ulh3What We're Looking For /h3ulli1+ years of experience in chargeback management, risk operations, e-commerce, or a related field. /liliUnderstanding of dispute and chargeback processes across payment providers such as PayPal, Stripe, Shopify Payments, and card networks. /liliStrong analytical skills with the ability to interpret data, identify trends, and make data-driven decisions. /liliExcellent attention to detail and organizational skills. /liliAbility to work independently, prioritize tasks, and perform well in a fast-paced environment. /liliStrong communication skills, with the ability to explain complex topics clearly to different audiences. /liliIntermediate level of English (written and spoken). /li /ulh3What We Offer /h3ulliPrivate health insurance. /liliProfessional growth and development opportunities. /liliRemote work on Fridays. /liliThe opportunity to join a fast-growing international TravelTech company. /li /ul /p #J-18808-Ljbffr

pSener is seeking a Fabrication Manager for Offshore Wind Projects to lead our team in Spain. The role focuses on ensuring safe and efficient fabrication activities, managing site teams, and ensuring compliance with quality standards. /ppThe ideal candidate has over 10 years of experience in fabrication oversight and a strong background in managing offshore wind or large-scale oil gas projects. Join us to work on innovative technological projects and enjoy flexible working hours and professional development opportunities. /p #J-18808-Ljbffr

Experteer Overview In this role you will lead aseptic and oral production operations, driving safety, quality and operational excellence within a regulated environment. You’ll manage a multidisciplinary team, ensure timely project milestones, and secure reliable supply across a global network. You will align with cGMP standards and regulatory expectations, fostering continuous improvement and cross-functional collaboration. This is a strategic leadership role with a focus on development, compliance and scalable production impact. Compensaciones / Beneficios • Lead and develop a multidisciplinary production team to deliver objectives • Ensure safe, high-performing, and compliant production operations aligned with cGMP • Manage budgets, resources, and risk to maintain efficient, sustainable processes • Drive timely decision-making and prioritization to hit project milestones • Oversee production documentation, validation, and training programs • Maintain compliance with internal standards and global regulatory requirements • Foster a safety culture and implement EHS practices including action plans • Promote continuous improvement and cross-functional collaboration across OneMP and global network • Support reliable market supply and seamless project transfers across the organization Responsabilidades • u003e6 years of leadership experience in Operations • Strong knowledge of pharmaceutical operations and aseptic manufacturing • Proficiency in cGMP regulations and quality systems • Excellent organizational, communication, and stakeholder management skills • University degree in Health Sciences, Pharmacy, Biopharmaceutical Sciences, Biology, or related field • Ability to motivate and develop people, drive innovation, and collaborate across functions and geographies Requisitos principales • Flexible working conditions • Life and accident insurance • Health insurance at a competitive price • Investment in your learning and development • Gym membership discounts

ppbJoin a leading global pharmaceutical company as an IT EDP Data Migration System Lead. /b You will drive enterprise data migration initiatives, leading the design, governance, and execution of scalable data solutions while collaborating with cross-functional teams and external partners to support key business transformation programs. This is an excellent opportunity to make a global impact in a highly innovative and data-driven environment. /pulliAct as the technical lead for Data Migration and Data Management initiatives across global programs. /liliDefine end-to-end migration strategies, architectures, frameworks, and technical standards. /liliOwn the overall solution design for data migration processes supporting ERP implementations, acquisitions, divestitures, and system transformations. /liliLead data discovery, data assessment, data object definition, and source-to-target mapping activities. /liliDrive data architecture decisions ensuring consistency across systems and platforms. /liliEnsure alignment between business processes, enterprise architecture standards, and migration solutions. /liliReview and approve technical designs, transformation rules, validation procedures, and reconciliation approaches. /liliDefine migration waves, cutover strategies, rollback procedures, and go-live readiness criteria. /liliEstablish best practices, methodologies, templates, and governance models for migration projects. /liliProvide technical leadership and mentoring to project teams, migration specialists, developers, and analysts. /liliCollaborate with Enterprise Architecture, Application Owners, Integration Teams, Data Governance, and Security organizations. /liliSupport solution scalability, maintainability, performance, and compliance requirements. /liliNetwork knowledge in order to be able to stablish the connections to source and target systems for each project where the Data Migration System is required. /liliCloud based ETL solutions architecture, prefereable in Amazon AWS services /liliLeva, GxP system validation knowledge /liliManual and Automated based Testing tools knowledge for testing new system requirements /liliSAP architecture SAP data model knowledge, no ABAP knowledge required, but RFC function and SAP BTP cockpit services /liliDatabase SQL querying tools knowledge /liliWindows Servers advanced knowledge /liliSpanish fluent /lili08/09h -17/18h from Monday to Friday (flexible) /lili4 days remote and 1 day on-site /liliSalary package based on your profile. We will discuss it on our first call. /liliPermanent Contract /liliTicket restaurant included in-office hours. /liliFlexible compensation plan (free of income tax) where we provide you with medical insurance, public transport ticket and childcare check. /liliDiscounts in gym network. /liliLearning Development /liliFriend Referral Program /li /ul /p #J-18808-Ljbffr

ph3Data Migration System Lead /h3 pOmega CRM Consulting is looking for a Data Migration System Lead to collaborate with one of the top global pharmaceutical companies. The role is responsible for leading the design, governance, and execution of enterprise data migration solutions while acting as the technical authority for data-related system implementations and transformations. /p pThis role combines deep expertise in data architecture, ERP data models, system integrations, data quality, and migration methodologies with strong project leadership capabilities. It serves as the primary technical lead across all migration phases, ensuring that business requirements are translated into scalable and sustainable solutions that support organizational objectives. The role works closely with Business Process Owners, Enterprise Architects, Master Data Teams, Analytics functions, and external implementation partners to ensure successful delivery of strategic initiatives. /p h3System Lead Responsibilities /h3 ul liAct as the technical lead for Data Migration and Data Management initiatives across global programs. /li liDefine end-to-end migration strategies, architectures, frameworks, and technical standards. /li liOwn the overall solution design for data migration processes supporting ERP implementations, acquisitions, divestitures, and system transformations. /li liLead data discovery, data assessment, data object definition, and source-to-target mapping activities. /li liDrive data architecture decisions ensuring consistency across systems and platforms. /li liEnsure alignment between business processes, enterprise architecture standards, and migration solutions. /li liReview and approve technical designs, transformation rules, validation procedures, and reconciliation approaches. /li liDefine migration waves, cutover strategies, rollback procedures, and go-live readiness criteria. /li liEstablish best practices, methodologies, templates, and governance models for migration projects. /li liProvide technical leadership and mentoring to project teams, migration specialists, developers, and analysts. /li liCollaborate with Enterprise Architecture, Application Owners, Integration Teams, Data Governance, and Security organizations. /li liSupport solution scalability, maintainability, performance, and compliance requirements. /li /ul h3Technical Skills /h3 ul liNetwork knowledge /li liCloud based ETL solutions architecture, preferabe in Amazon AWS services /li liLeva, GxP system validation knowledge /li liManual and Automated based Testing tools /li liSAP architecture knowledge /li /ul h3What We Offer /h3 ul liPermanent contract. /li liFlexible schedule. We make it easy. Balance your professional and personal life. /li liTrainings Certifications. Improve your skills and get the official certificate from our main partners. /li liHome Office. /li liFlexible retribution (public transport ticket, Ticket restaurant, ...). /li liHealth insurance. /li liOMEGA in action. Our commitment to a better society is not just an intention. /li /ul /p #J-18808-Ljbffr

QA SENIOR MANAGER / QP DEPUTY ALMIRALLPresenta candidaturaremote type: Industrial Operationslocations: SANT ANDREU DE LA BARCAtime type: Full timeposted on: Offerta pubblicata 3 giorni fatime left to apply: Data fine: 31 agosto 2026 (30+ giorni rimanenti per candidarsi)job requisition id: Stiamo costruendo il futuro della dermatologia medica concentrandoci sui bisogni ancora insoddisfatti dei pazienti e dando alle persone lo spazio per pensare in modo indipendente, assumersi responsabilità e generare un impatto che conta davvero.Il nostro purpose è semplice: trasformare la vita dei pazienti rispondendo a bisogni reali. Lavoriamo con rigore, agiamo con coraggio, teniamo le cose semplici e orientiamo l’innovazione dove può davvero fare la differenza.Riconosciuti come Top Employer in Spagna dal 2008 e in Germania dal 2025, continuiamo a investire in un ambiente in cui le persone possono crescere e andare avanti.Se pensi in modo diverso, qui è il posto giusto per te.## Quality Assurance Senior Manager – GDP/GMP Transport Quality¿Te apasiona la calidad farmacéutica y quieres formar parte de una compañía internacional donde tu trabajo contribuya directamente a garantizar que los medicamentos lleguen a los pacientes con los más altos estándares de calidad y cumplimiento normativo?Buscamos un/a Quality Assurance Senior Manager para incorporarse a nuestro equipo y liderar la gestión de calidad asociada al transporte y distribución de medicamentos a nivel global.## Tu misiónSerás responsable de asegurar el cumplimiento de las normativas GMP/GDP en todos los procesos relacionados con la distribución de las especialidades farmacéuticas del Grupo, garantizando los máximos niveles de calidad, seguridad y compliance en la cadena de suministro.Además, tendrás la oportunidad de desarrollarte para actuar como back-up de la Responsible Person de Almirall S.A. en su función como Titular de la Autorización de Comercialización.## ¿Cómo será tu día a día? Definir, implementar y mantener procedimientos y directrices corporativas relacionados con el transporte y distribución de productos farmacéuticos. Garantizar la actualización de los procesos conforme a la regulación sanitaria vigente y a las mejores prácticas del sector. Homologar, evaluar y realizar el seguimiento de proveedores logísticos y empresas de transporte mediante auditorías, gestión contractual y control de calidad. Supervisar la validación y el cumplimiento normativo de los procesos de transporte a nivel global. Gestionar desviaciones, incidencias y planes de acción relacionados con la calidad del transporte. Colaborar con equipos internacionales y áreas transversales como Compras, International Trade y Local Quality Responsibles. Participar activamente en inspecciones regulatorias y auditorías de partners, representando las áreas bajo tu responsabilidad. Definir y monitorizar KPIs de calidad y eficiencia, impulsando iniciativas de mejora continua.## Lo que buscamos### Formación Licenciatura o Grado en Farmacia. Conocimiento sólido de normativas GMP y GDP.### Experiencia* Entre 3 y 5 años de experiencia en Garantía de Calidad, Producción y/o Control de Calidad dentro de la industria químico-farmacéutica. Experiencia trabajando en entornos regulados. Se valorará experiencia con TrackWise u otras herramientas de gestión de calidad.### Idiomas Inglés avanzado (entorno internacional).## Competencias clave Orientación a la calidad y al cumplimiento normativo. Capacidad para desarrollar y mantener procedimientos corporativos. Experiencia en auditorías y gestión de proveedores. Pensamiento analítico y enfoque de mejora continua. Habilidades de colaboración e influencia en entornos multiculturales.* Visión transversal del negocio y orientación a resultados.## ¿Qué encontrarás en este reto? Un entorno internacional y multicultural. Exposición global dentro de la cadena de suministro farmacéutica. Participación directa en proyectos de impacto para la calidad y seguridad de los medicamentos. Oportunidades de desarrollo profesional en el ámbito de Quality Assurance y Compliance.¿Te gustaría contribuir a que los medicamentos lleguen a millones de pacientes con los más altos estándares de calidad? ¡Queremos conocerte! CENTRO TRABAJO: SABGRUPO PROFESIONAL: 6TIPO DE CONTRATO: IndefinidoHORARIO: Central Flexbr#J-18808-Ljbffr

QA SENIOR MANAGER / QP DEPUTY ALMIRALLBewerbenremote type: Industrial Operationslocations: SANT ANDREU DE LA BARCAtime type: Full timeposted on: Vor 5 Tagen ausgeschriebentime left to apply: Enddatum: 31. August 2026 (Noch 30+ Tage Zeit für Bewerbung)job requisition id: Warum Almirall?Wir gestalten die Zukunft der medizinischen Dermatologie, indem wir uns auf unerfüllte Bedürfnisse von Patient:innen konzentrieren und Menschen den Raum geben, eigenständig zu denken, Verantwortung zu übernehmen und Wirkung zu erzielen, die wirklich zählt.Unser Anspruch ist klar: das Leben von Patient:innen zu verbessern, indem wir auf echte Bedürfnisse eingehen. Wir arbeiten mit Präzision, handeln mutig, halten die Dinge einfach und richten unsere Innovation dort aus, wo sie wirklich einen Unterschied macht.Als Top Employer in Spanien seit 2008 und in Deutschland seit 2025 investieren wir kontinuierlich in ein Umfeld, in dem Menschen wachsen und vorankommen können.Wenn du Dinge anders angehst, bist du hier richtig.## Quality Assurance Senior Manager – GDP/GMP Transport Quality¿Te apasiona la calidad farmacéutica y quieres formar parte de una compañía internacional donde tu trabajo contribuya directamente a garantizar que los medicamentos lleguen a los pacientes con los más altos estándares de calidad y cumplimiento normativo?Buscamos un/a Quality Assurance Senior Manager para incorporarse a nuestro equipo y liderar la gestión de calidad asociada al transporte y distribución de medicamentos a nivel global.## Tu misiónSerás responsable de asegurar el cumplimiento de las normativas GMP/GDP en todos los procesos relacionados con la distribución de las especialidades farmacéuticas del Grupo, garantizando los máximos niveles de calidad, seguridad y compliance en la cadena de suministro.Además, tendrás la oportunidad de desarrollarte para actuar como back-up de la Responsible Person de Almirall S.A. en su función como Titular de la Autorización de Comercialización.## ¿Cómo será tu día a día? Definir, implementar y mantener procedimientos y directrices corporativas relacionados con el transporte y distribución de productos farmacéuticos. Garantizar la actualización de los procesos conforme a la regulación sanitaria vigente y a las mejores prácticas del sector. Homologar, evaluar y realizar el seguimiento de proveedores logísticos y empresas de transporte mediante auditorías, gestión contractual y control de calidad. Supervisar la validación y el cumplimiento normativo de los procesos de transporte a nivel global. Gestionar desviaciones, incidencias y planes de acción relacionados con la calidad del transporte. Colaborar con equipos internacionales y áreas transversales como Compras, International Trade y Local Quality Responsibles. Participar activamente en inspecciones regulatorias y auditorías de partners, representando las áreas bajo tu responsabilidad. Definir y monitorizar KPIs de calidad y eficiencia, impulsando iniciativas de mejora continua.## Lo que buscamos### Formación Licenciatura o Grado en Farmacia. Conocimiento sólido de normativas GMP y GDP.### Experiencia* Entre 3 y 5 años de experiencia en Garantía de Calidad, Producción y/o Control de Calidad dentro de la industria químico-farmacéutica. Experiencia trabajando en entornos regulados. Se valorará experiencia con TrackWise u otras herramientas de gestión de calidad.### Idiomas Inglés avanzado (entorno internacional).## Competencias clave Orientación a la calidad y al cumplimiento normativo. Capacidad para desarrollar y mantener procedimientos corporativos. Experiencia en auditorías y gestión de proveedores. Pensamiento analítico y enfoque de mejora continua. Habilidades de colaboración e influencia en entornos multiculturales.* Visión transversal del negocio y orientación a resultados.## ¿Qué encontrarás en este reto? Un entorno internacional y multicultural. Exposición global dentro de la cadena de suministro farmacéutica. Participación directa en proyectos de impacto para la calidad y seguridad de los medicamentos. Oportunidades de desarrollo profesional en el ámbito de Quality Assurance y Compliance.¿Te gustaría contribuir a que los medicamentos lleguen a millones de pacientes con los más altos estándares de calidad? ¡Queremos conocerte! CENTRO TRABAJO: SABGRUPO PROFESIONAL: 6TIPO DE CONTRATO: IndefinidoHORARIO: Central Flexbr#J-18808-Ljbffr

pAlmirall, S.A in Sant Feliu de Llobregat is seeking a QA Senior Manager to maintain and improve the GVP Quality Management System, ensuring compliance with ICH, EU GVP modules, and pharmacovigilance regulations. /ppYou will lead audits, inspections, and QA activities with internal and external partners, fostering continuous improvement while coordinating with safety teams. Fluent English and strong regulatory expertise are required. /p #J-18808-Ljbffr

ph3Sales Compensation Planning Expert /h3pHP is seeking a Sales Planning Expert – Quota Coverage Strategy to lead the design, governance, and continuous improvement of global sales planning processes across the channel business. The role owns the end‑to‑end quota and sales coverage strategy, aligning financial targets, sales capacity, and market potential while driving standardization, automation, and best practices globally. It sits at the intersection of Sales, Finance, and Sales Compensation, enabling scalable, data‑driven planning across HP’s multi‑channel go‑to‑market model in line with internal SPM transformation priorities. /ph3Key Responsibilities /h3ullibQuota Coverage Strategy Leadership /b – Define and evolve HP’s global sales coverage and quota deployment strategy for channel business, ensuring coverage design is defined upfront and aligned with quota deployment timelines. Drive integration of territory design, account segmentation, and quota allocation into a consistent planning framework; establish standard coverage models and role definitions aligned to HP’s go‑to‑market and partner ecosystem. /lilibQuota Planning Deployment Excellence /b – Lead global quota planning cycles across regions, RTMs, and sales roles, ensuring alignment with financial targets and strategic priorities. Design and implement robust quota methodologies that consider sales potential, rep workload, role seniority, and specialization. Drive ongoing quota rebalancing processes to reflect business changes and ensure global consistency in quota deployment processes, governance, and timelines. /lilibProcess Standardization Transformation /b – Lead the definition and rollout of sales planning standards and best practices globally, including standard quota dimensions, deployment granularity, role and plan rationalization, and interlock processes across Sales, Finance, and Compensation. Drive end‑to‑end process simplification and automation, reducing reliance on manual workflows, and support implementation of integrated SPM tools and data architectures. /lilibAnalytics, Modeling Insights /b – Develop advanced coverage and quota modeling capabilities, including scenario planning and optimization. Leverage data, analytics, and AI/ML to assess customer/partner potential, optimize coverage and quota allocation, improve forecasting accuracy and ROI, and establish KPIs for quota accuracy, coverage effectiveness, and sales productivity. /lilibGovernance Cross‑Functional Alignment /b – Act as a global point of accountability for sales planning governance, ensuring consistency and compliance. Drive alignment across Sales leadership, Finance, and Sales Compensation, and enable structured quota change control and governance frameworks. /lilibContinuous Improvement Best Practice Evolution /b – Identify and drive process improvement opportunities based on field feedback and performance insights, promoting industry best practices in coverage design and sales planning efficiency. Lead initiatives to improve planning speed, data quality, and end‑user experience. /li /ulh3Required Qualifications /h3ulli5‑10+ years of experience in sales planning, sales compensation, or sales operations in a global environment. /liliDeep expertise in quota setting methodologies, sales coverage and territory design, and channel business models with partner ecosystems. /liliProven track record delivering global process standardization and transformation programs. /liliStrong analytical capabilities with experience in data‑driven planning and modeling. /liliFluency in Business English (written and verbal). /liliBachelor or Master’s degree in Finance, Economics or a related field. /liliExperience working in complex, matrixed organizations with multiple RTMs and sales roles. /liliAbility to influence senior stakeholders across Sales, Finance and Operations. /li /ulh3Preferred Qualifications /h3ulliExperience with SPM tools such as Anaplan, Forma/Varicent and sales analytics platforms. /liliKnowledge of AI/ML‑based planning approaches. /liliExperience in large‑scale sales transformation programs. /liliFamiliarity with quota governance frameworks and financial planning integration. /li /ulh3Success Criteria (12–18 months) /h3ulliImproved quota accuracy and fairness across channel roles. /liliReduced quota deployment cycle time and manual effort. /liliIncreased coverage effectiveness and sales productivity. /liliAdoption of standardized planning processes globally. /liliStrong alignment between Finance targets and Sales execution. /liliSales and Services Entity (ES11) alignment of deliverables. /li /ulh3Equal Opportunity Employer /h3pHP, Inc. provides equal employment opportunity to all employees and prospective employees, without regard to race, color, religion, sex, national origin, ancestry, citizenship, sexual orientation, age, disability, or status as a protected veteran, marital status, familial status, physical or mental disability, medical condition, pregnancy, genetic predisposition or carrier status, uniformed service status, political affiliation or any other characteristic protected by applicable national, federal, state, or local law(s). You will not be subject to any adverse treatment if you choose to disclose the information requested. The information obtained will be kept in strict confidence. For more information, review HP’s EEO Policy or read about your rights as an applicant under the law here:Know Your Rights: Workplace Discrimination is Illegal. /p /p #J-18808-Ljbffr

QA SENIOR MANAGERSolicitarremote type: Industrial Operationslocations: SANT FELIU DE LLOBREGAT: SANT ANDREU DE LA BARCA: GLOBALtime type: Full timeposted on: Publicado hace 5 díastime left to apply: Fecha final: 31 de agosto de 2026 (Quedan más de 30 días para realizar la solicitud)job requisition id: Estamos construyendo el futuro de la dermatología médica centrándonos en las necesidades no cubiertas de los pacientes y dando a las personas el espacio para pensar de forma independiente, asumir responsabilidades y generar un impacto que de verdad importe.Nuestro propósito es sencillo: transformar la vida de los pacientes abordando necesidades reales. Trabajamos con rigor, actuamos con valentía, simplificamos lo complejo y enfocamos la innovación allí donde realmente marca la diferencia.Reconocidos como Top Employer en España desde 2008 y en Alemania desde 2025, seguimos invirtiendo en un entorno donde las personas pueden crecer y avanzar.Si quieres hacer las cosas de otra manera, este es tu lugar.MissionResponsible for the maintenance, development and continuous improvement of the Almirall GVP Quality Management System ensuring compliance with applicable regulations and guidelines.Functions and responsibilities1. To maintain the Quality System for Pharmacovigilance activities in accordance with Almirall policies, ICH guidelines, EU GVP modules, and other relevant regulatory requirements with the support of the Almirall Corporate Patient Safety department.2. To set up the GVP risk-based audit plan and program and perform (or coordinate and oversee when outsourced) audits at affiliates, partners, CROs/vendors as well as internal audits to the Almirall Pharmacovigilance System on a regular basis.3. To report the observations arising from audits (or any other quality issue) to applicable management and follow-up on the significant findings until completion.4. To lead the preparation and management of inspection by Competent Authorities and audits by third parties to Almirall by developing an inspection readiness plan.5. To edit, review and approve the procedures and any other key documents ensuring that they are aligned and compliant with the applicable regulation applicable to Drug Safety.6. To select, coordinate and oversee the outsourced QA activities applicable to pharmacovigilance (e.g. audits, mock inspections, training).7. Involvement in due diligence of development products, as needed.8. To promote the continuous improvement of the GVP Quality System based on audit findings and changes in regulatory requirements.EducationLife science degree (Pharmacy, Chemistry, Biology, etc.)Specific expertise- Knowledge of GVP's, GMP's and GCP's, drug safety, clinical trials, data management, pharmacokinetics, and statistics.- EU and non-EU regulations applicable to pharmacovigilance.- Training in Quality Assurance, specifically RD areas.- Proficiency in English languageINFORMACIÓN ADICIONAL- CENTRO DE TRABAJO: RD - SANT FELIU DE LLOBREGAT- TIPO DE CONTRATO: Indefinido- GRUPO PROFESIONAL: 6- HORARIO: Central FlexQA RD CPD - GVP Quality Assurance Senior Managerbr#J-18808-Ljbffr

pNovartis Farmacéutica, S.A. in Barcelona is seeking Associate Director, Aggregate Reports Risk Management to lead AR RM operations across the product portfolio, ensuring compliance and cross-functional collaboration. /ppYou will develop and maintain the global aggregate reporting schedule, monitor KPIs, and drive investigations and CAPA; act as a key operational interface with Country Organisations and partners. Hybrid work model in Barcelona; fluent English required. /p #J-18808-Ljbffr

ppAt Roche Diagnostics Solutions (RDS), our mission is clear: to diagnose earlier, develop faster, and personalise treatment because every patient is unique. Our Clinical Development Medical Affairs (CDMA) team drives innovation to improve healthcare outcomes globally. /p h3Position Overview /h3 pAs a Clinical Site Manager for Continuous Glucose Monitoring studies in our Study Delivery Near Patient Care CVMD team, you are responsible for designing, planning, coordinating, and conducting all activities involved in initiating, monitoring, and completing clinical research studies at the clinical study sites. You ensure studies are delivered, recorded, and reported in accordance with protocol, standard operating procedures, good clinical practices, and other applicable regulatory requirements. /p h3Responsibilities /h3 ul liAct as the primary contact and clinical trial expert for assigned study site personnel, coordinating training, certification, and providing technical assistance to ensure successful study execution. /li liPerform site assessments and qualification visits to support the site selection decision process and site activation activities, including contracting and obtaining IRB/EC/Health Authority approvals in compliance with regulatory requirements. /li liDevelop and manage key study site documentation such as Study Monitoring Plans, informed consent documents, source documents, patient instruction guides, and case report forms, while contributing technical expertise to review study protocols, data management plans, reports, and manuscripts. /li liOversee CROs for the delivery of site management activities, including training CRO CRAs, escalating issues, and collaborating with international investigators and key customers while mentoring and supporting colleagues to enhance their skills and expertise. /li liExecute site management activities for sponsored studies in assigned focus areas across all phases of study (start‑up, conduct, and close‑out) for both registrational and non‑registrational purposes. /li liValidate product performance claims, supply data for critical regulatory submissions, define the functional and clinical utility of products, and gather feedback and opinions from laboratories or customers regarding the products. /li liWork in local and global study teams, including virtual teams, demonstrating diversity, cultural awareness, and fostering strong, collaborative relationships with cross‑functional team members, internal stakeholders, and external partners to achieve business goals and ensure operational excellence. /li /ul h3Qualifications /h3 ul liBachelor’s degree in Science, preferably in Health Sciences such as Clinical Diagnostics or Engineering (or equivalent combination of education and work experience). /li liWorking experience in the Medical Device or Diagnostics industry, and solid experience in clinical study of IVD/Medical Device/Drug. /li liExperience particularly in the Continuous Glucose Monitoring field. /li liExcellent understanding of ISO14155:2026, MDR, and ICH GCP guidelines in the execution of clinical trials. /li liAbility to make sound decisions, analyze and solve problems, and take responsibility for independent choices. /li liDemonstrates flexibility and adaptability to perform in a fast‑paced, matrixed environment where fluid, cross‑team collaboration is crucial. /li /ul pWhere pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Motherwell. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process. /p pbRoche is an Equal Opportunity Employer. /b /p /p #J-18808-Ljbffr