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Experteer Overview In this role you develop and optimize tools and automation for coating application, collaborating with cross-functional teams to translate needs into tested, scalable solutions. You’ll work with internal and external stakeholders to ensure safe, reliable field implementation. The position centers on hands-on tool development, integration of mechanical and electrical components, and driving repeatable, high-quality application methods. This is an opportunity to shape tooling in a global, impact-focused coatings company. Compensaciones / Beneficios • Develop, prototype, and enhance tools and equipment for coating application, emphasizing automated and semi-automated solutions • Support manufacturability, serviceability, and safe operation in industrial coating environments • Contribute to automated coating concepts by integrating mechanical parts, electronics, sensors, actuators, and control elements • Test, troubleshoot, and optimize tool performance in lab, workshop, and field settings • Assist in selecting and validating components and suppliers for tool projects • Prepare drawings, specs, test plans, and development documentation for new tools or modifications • Coordinate with application specialists, coating advisors, Ru0026D, and vendors to ensure timely delivery and practical implementation • Contribute to continuous improvement of application methods, reliability, and repeatability in automated coating processes • Deliver fit-for-purpose tools and equipment and ensure on-time milestones and documentation • Enhance reliability, repeatability, and safety in coating application processes • Support automation initiatives and field implementation Responsabilidades • Bachelor in Mechanical Engineering • 3-7 years in product/tool development, industrial equipment, automation, or related fields • Hands-on mechanical design and/or electronics integration • Experience with testing, troubleshooting, root cause analysis, and documentation • Knowledge of automation, robotics, or coating application processes (advantage) • Fluency in English Requisitos principales •

Experteer Overview In this role you will shape and manage the virtualization and Wintel infrastructure to support Grifols’ global IT landscape. You will serve as the Technical Product Owner for core platforms, driving roadmaps, improvements, and best practices. You’ll lead cross-functional initiatives, coordinate with providers, and maintain strong client relationships to ensure reliable, scalable systems that underpin critical healthcare operations. This is a chance to influence high-availability environments at a world‑leading pharmaceutical company. Compensaciones / Beneficios • Act as Technical Product Owner for Wintel and Virtualization platforms, guiding roadmap and lifecycle • Define and implement technical roadmaps and best practices • Optimize global infrastructure and drive continuous improvement • Collaborate on cross-strategic projects and ensure timely, budget-conscious delivery • Supervise providers and maintain positive client/colleague relationships • Provide technical reference within the company to enable informed decision-making Responsabilidades • Bachelor’s degree in Information Technology, Computer Science, or related field • Strong communication, conflict resolution, problem-solving skills • Team player with collaborative mindset • Analytical with prioritization and decision-making abilities based on impact • Polyvalent, eager to learn and adapt • Deep operational knowledge in high-availability environments (e.g., Stretched Clusters, Disaster Recovery) • Technical knowledge of Wintel technologies (Windows Server, Clusters, Windows Admin Center) and related services (DNS, DFS, NAS, File Service, IIS, FTP, Printer) • Experience with Automation and Infrastructure as Code tools (Terraform, Ansible) • Strong server hardware knowledge; SME / senior specialist experience • In-depth knowledge of VMware and Nutanix, Wintel and infrastructure best practices • Scripting skills (PowerShell, Bash) • Knowledge of Networks, Security, Storage, and Backup systems • High level of spoken and written English Requisitos principales • Hybrid work model • Flexible schedule • Benefits package • Permanent contract • Career development opportunities

Experteer Overview In this role you will lead the design, planning and delivery of office refurbishment and fit-out projects across multiple locations to optimize space use, ensure regulatory compliance, and maintain budget alignment with Grifols strategy. You will collaborate with Facilities, IT and Security, coordinate with external vendors, and manage multi-site projects. The role emphasizes continuous improvement of design and execution processes and requires travel between sites. This is a chance to shape efficient, compliant workplaces within a global healthcare company. Compensaciones / Beneficios • End-to-end management of office refurbishment and fit-out projects across multiple locations • Design and planning of corporate spaces tailored to local needs • Coordinate with internal and external stakeholders (Facilities, IT, Security, suppliers) • Monitor budgets and timelines to meet deadlines and cost controls • Site supervision and validation of corporate standards • Risk management and issue resolution throughout projects • Continuous improvement of design and execution processes Responsabilidades • Bachelor’s or Master’s degree in Architecture, Building Engineering, Engineering or related field • Project Management certification is a plus • 3–5 years of experience in managing office, retail or corporate space projects • Experience in managing multi-site projects is highly desirable • Strong background in coordinating multidisciplinary teams and external vendors • Proficiency in AutoCAD or similar design tools • Experience in budget management and project scheduling • Site supervision and construction management experience • Fluent English (minimum B2/C1) • Strong organizational, communication and stakeholder management skills • Problem-solving abilities and adaptability • Continuous improvement mindset • Willingness to travel 15%–50% Requisitos principales • Permanent contract • Flexible schedule • Occasional remote work • Location: Parets del Vallès, Spain • Benefits package • Global, inclusive culture

pNovartis is seeking an Associate Director to build and lead a Barcelona-based team for Clinical Data Analytics and Technology. You will guide a small agile team, connect with global colleagues, and turn strategic priorities into practical data, analytics, and technology solutions across clinical trial delivery. /ppThe role emphasizes AI-driven innovation, risk-based quality management, and compliance with GxP, GDPR, and data governance standards, with a mix of onsite and hybrid work at the /p #J-18808-Ljbffr

Experteer Overview You will own and evolve the As-Is and Target Architecture for the Supply Chain domain, aligning business capabilities with the application landscape. In this role you act as a technical authority, guiding decisions and shaping long-term direction across sectors. You’ll partner with Business and Solution Architects and senior stakeholders to reduce technical debt, simplify and innovate, while keeping the landscape secure and aligned with priorities. This is a chance to influence enterprise strategy at the intersection of business understanding and architecture, delivering measurable impact. Compensaciones / Beneficios • Define and continually evolve the As-Is and Target Architecture for the Supply Chain domain • Drive a harmonized cross-sector view linking business capabilities to applications • Provide expert input to Architecture Governance Boards and influence governance decisions • Shape long-term direction of a critical business domain • Collaborate with Business Architects, Solution Architects, and senior stakeholders to reduce technical debt • Identify opportunities for simplification and innovation while maintaining stability and security of the landscape • Translate complex architectural concepts into clear, actionable decisions • Balance strategic guidance with pragmatic delivery to support priorities Responsabilidades • 5+ years of experience in Enterprise, Domain, or Solution Architecture in complex IT environments • Proven track record shaping and governing domains at cross-functional or cross-sector levels • Solid understanding of Supply Chain processes and related application landscapes • Experience in architecture modeling, target architecture development, and application portfolio planning • Ability to prepare and support decisions in architecture governance forums • Strong analytical and problem-solving skills • Business-fluent English, written and spoken Requisitos principales •

Experteer Overview In this Analytics Architect role, you design and deliver scalable data and AI solutions to power smarter work practices across the organization. You’ll join a cross-border team delivering analytics and data products within a product-oriented delivery model. You’ll own data platforms, promote governance and security, and translate business needs into technical solutions. The role spans diverse AI use cases, including automation and procurement intelligence, contributing to a global, innovative data culture. Compensaciones / Beneficios • Design, build, and maintain scalable data pipelines and platform components • Develop interfaces that replace manual processes with intuitive experiences • Own data platforms with focus on governance, security, and full lifecycle compliance • Collaborate with delivery pod stakeholders to shape technical direction • Shape future data engineering within Enabling Functions leveraging Snowflake, AWS, and Palantir Foundry • Contribute to a Spain-based hub and high-visibility AI use cases across organization Responsabilidades • 4–8 years of software engineering experience in enterprise environments • Proficiency in Python and Spark • Experience with CI/CD, version control, and automated testing • Hands-on with Palantir Foundry, Snowflake, and PySpark • Understanding of data pipeline architecture, data governance, privacy, and security in enterprises • Strong communication of technical concepts to non-technical stakeholders • University degree or equivalent in a technical field • Willingness to work in a distributed international team and travel in Europe • Familiarity with AI workflows, MLOps, AI safety, or CI/CD for AI is a plus Requisitos principales •

The Associate Director, Scientific Content (Neuroscience) is a strategic and execution-focused role within the International Medical Centre of Excellence (IMACE), accountable for supporting the planning, development, and delivery of high-quality scientific and medical content for the Neuroscience (NS) portfolio. Reporting to the Head of Scientific Content Portfolio (NS), this role plays a critical part in translating International Medical and Therapeutic Area (TA) strategies into clear, actionable scientific communication plans and content roadmaps. The Associate Director ensures that scientific and medical materials are scientifically robust, aligned with NS medical objectives, and delivered in a timely and consistent manner across regions and countries. Working closely with IMACE colleagues, International Medical Affairs (IMA), Global Medical Affairs (GMA), cross-functional partners and countries, this role supports the coordinated execution of scientific content strategies, contributes to launch readiness and lifecycle activities, and helps maintain a coherent and high-quality scientific narrative across channels. The Associate Director also contributes to continuous improvement by enabling scalable content development approaches, supporting governance and quality standards, and leveraging insights from markets to refine and enhance scientific communication. Through strong collaboration and operational leadership, this role helps ensure that NS scientific content effectively supports scientific engagement, medical excellence, and evolving stakeholder needs. La siguiente información tiene como objetivo proporcionar a los posibles candidatos una mejor comprensión de los requisitos para este puesto. Location Barcelona, Spain (Hybrid) Key Responsibilities • Strategic Enablement & Portfolio Execution: Support the team in defining and delivering the Scientific Content pillar strategy, objectives, metrics, and key initiatives for the NS portfolio. Translate International Medical and NS TA strategies into clear, executable scientific content plans and roadmaps aligned to product lifecycle and evidence plans. Provide portfolio-specific insights to shape scientific communication strategies, including execution considerations and prioritization recommendations. Monitor the external NS scientific landscape and proactively flag emerging data, competitive developments, and content implications. Prepare portfolio updates, content strategy reviews, and materials for governance forums, leadership reviews, and planning cycles., • Scientific Content Development & Delivery: Support the planning, coordination, and delivery of high-quality, compliant scientific and medical materials across the NS portfolio (e.g. slide decks, iSEC, core HCP materials, MSL training). Ensure all content is scientifically accurate and aligned with approved labels, positioning, and evidence. Ensure consistent application of content frameworks, templates, modular content principles, and reuse strategies. Provide scientific and strategic oversight of complex or high-priority materials, including launch-critical content. Support launch readiness and lifecycle activities through proactive management of timelines, dependencies, and delivery milestones., • Cross-Functional & Stakeholder Collaboration: Partner closely with IMACE, IMA, GMA TA teams and other stakeholders to define content needs, key messages, and fit-for-purpose solutions. Act as the primary NS content interface for regions and countries, supporting localization while maintaining strategic alignment and scientific integrity. Incorporate field insights and feedback to continuously refine and improve content. Support optimization of content formats, personalization, and channel delivery to enhance engagement and customer experience. Coordinate with agencies/vendors as a day-to-day scientific content partner (e.g., briefing, review cycles, scientific direction), as applicable., • Compliance, Governance & Quality: Ensure all NS scientific content complies with applicable regulations, company policies, SOPs, and industry standards. Apply and reinforce content governance and review processes to enable timely, high-quality approvals. Partner with Medical Writing, Scientific Operations, Legal, Compliance, and Regulatory teams to support efficient content development. Champion scientific rigor, ethical standards, and quality across all content activities., • Leadership, Culture & Capability Building: Role model IMACE values and ways of working, fostering collaboration, accountability, and continuous improvement. Support the team in building a high-performing Scientific Content team culture rooted in scientific excellence and ownership. Support team members and partners, contributing to onboarding, capability building, and knowledge sharing., • Operational Excellence & Continuous Improvement: Drive operational excellence across NS content planning, development, review, and deployment. Enable scalable, modular content approaches to support reuse, localization, and rapid response to emerging data.Essential Requirements, • Education: Advanced degree in life sciences/healthcare (e.g., PhD, PharmD, MD) or equivalent., • 5+ years of experience in pharmaceutical, healthcare, or life sciences organizations, with a substantial focus on Medical Affairs and Scientific Content., • Strong track record in designing and overseeing development of a wide range of assets, including slide decks, training materials, congress materials, digital assets, and omnichannel content., • Demonstrated success in developing and executing scientific content and communication strategies, including launch and lifecycle communications, at an international scale., • Experience across both country-level and regional/global roles., • Ability to work independently and collaboratively, strong leadership and organizational skills, and able to drive multiple projects to successful, timely completion., • Proven experience collaborating with cross-functional partners and managing external vendors or agencies., • Fluent oral and written English required. Additional country or regional language(s) desirable.Desirable Requirements, • Previous experience in neuroscience therapeutic area.Benefits, • Read our handbook to learn about all the ways we'll help you thrive personally and professionally:, • Novartis Life Handbook, • Expected Annual Base Salary Range for role: 73,1 ,700.00 EUR, • The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically., • In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters., • The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs., • In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave., • Long-term equity awards granted at group level may also be part of your package., • Further details will be provided during the application process., • Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. xkdbapo Commitment to Diversity & Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. #J-18808-Ljbffr

Salary Range: €73,100.00 - €135,700.00 Band Level 5 Job Description Summary #LI-Hybrid Location: Barcelona, Spain Usted podría ser el solicitante perfecto para este trabajo. Lea toda la información asociada y asegúrese de presentar su candidatura. The Associate Director, Scientific Content (Neuroscience) is a strategic and execution‐focused role within the International Medical Centre of Excellence (IMACE), accountable for supporting the planning, development, and delivery of high‐quality scientific and medical content for the Neuroscience (NS) portfolio. Reporting to the Head of Scientific Content Portfolio (NS), this role plays a critical part in translating International Medical and Therapeutic Area (TA) strategies into clear, actionable scientific communication plans and content roadmaps. The Associate Director ensures that scientific and medical materials are scientifically robust, aligned with NS medical objectives, and delivered in a timely and consistent manner across regions and countries. Working closely with IMACE colleagues, International Medical Affairs (IMA), Global Medical Affairs (GMA), cross‐functional partners and countries, this role supports the coordinated execution of scientific content strategies, contributes to launch readiness and lifecycle activities, and helps maintain a coherent and high‐quality scientific narrative across channels. The Associate Director also contributes to continuous improvement by enabling scalable content development approaches, supporting governance and quality standards, and leveraging insights from markets to refine and enhance scientific communication. Through strong collaboration and operational leadership, this role helps ensure that NS scientific content effectively supports scientific engagement, medical excellence, and evolving stakeholder needs. Job Description Key Responsibilities: • Strategic Enablement & Portfolio Execution: Support the team in defining and delivering the Scientific Content pillar strategy, objectives, metrics, and key initiatives for the NS portfolio. Translate International Medical and NS TA strategies into clear, executable scientific content plans and roadmaps aligned to product lifecycle and evidence plans. Provide portfolio‐specific insights to shape scientific communication strategies, including execution considerations and prioritization recommendations. Monitor the external NS scientific landscape and proactively flag emerging data, competitive developments, and content implications. Prepare portfolio updates, content strategy reviews, and materials for governance forums, leadership reviews, and planning cycles., • Scientific Content Development & Delivery: Support the planning, coordination, and delivery of high‐quality, compliant scientific and medical materials across the NS portfolio (e.g. slide decks, iSEC, core HCP materials, MSL training). Ensure all content is scientifically accurate and aligned with approved labels, positioning, and evidence. Ensure consistent application of content frameworks, templates, modular content principles, and reuse strategies. Provide scientific and strategic oversight of complex or high‐priority materials, including launch‐critical content. Support launch readiness and lifecycle activities through proactive management of timelines, dependencies, and delivery milestones., • Cross‐Functional & Stakeholder Collaboration: Partner closely with IMACE, IMA, GMA TA teams and other stakeholders to define content needs, key messages, and fit‐for‐purpose solutions. Act as the primary NS content interface for regions and countries, supporting localization while maintaining strategic alignment and scientific integrity. Incorporate field insights and feedback to continuously refine and improve content. Support optimization of content formats, personalization, and channel delivery to enhance engagement and customer experience. Coordinate with agencies/vendors as a day‐to‐day scientific content partner (e.g., briefing, review cycles, scientific direction), as applicable., • Compliance, Governance & Quality: Ensure all NS scientific content complies with applicable regulations, company policies, SOPs, and industry standards. Apply and reinforce content governance and review processes to enable timely, high‐quality approvals. Partner with Medical Writing, Scientific Operations, Legal, Compliance, and Regulatory teams to support efficient content development. Champion scientific rigor, ethical standards, and quality across all content activities., • Leadership, Culture & Capability Building: Role model IMACE values and ways of working, fostering collaboration, accountability, and continuous improvement. Support the team in building a high‐performing Scientific Content team culture rooted in scientific excellence and ownership. Support team members and partners, contributing to onboarding, capability building, and knowledge sharing., • Operational Excellence & Continuous Improvement: Drive operational excellence across NS content planning, development, review, and deployment. Enable scalable, modular content approaches to support reuse, localization, and rapid response to emerging data.Essential Requirements:, • Education: Advanced degree in life sciences/healthcare (e.g., PhD, PharmD, MD) or equivalent., • 5+ years of experience in pharmaceutical, healthcare, or life sciences organizations, with a substantial focus on Medical Affairs and Scientific Content., • Strong track record in designing and overseeing development of a wide range of assets, including slide decks, training materials, congress materials, digital assets, and omnichannel content., • Demonstrated success in developing and executing scientific content and communication strategies, including launch and lifecycle communications, at an international scale., • Experience across both country-level and regional/global roles., • Ability to work independently and collaboratively, strong leadership and organizational skills, and able to drive multiple projects to successful, timely completion., • Proven experience collaborating with cross‐functional partners and managing external vendors or agencies., • Fluent oral and written English required., • Additional country or regional language(s) desirable.Desirable Requirements:, • Previous experience in neuroscience therapeutic area.Benefits:, • Read our handbook to learn about all the ways we'll help you thrive personally and professionally: Novartis Life Handbook, • Expected Annual Base Salary Range for role: 73,1 ,700.00 EUR, • The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically., • In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters., • The rewards of being part of our team go far beyond base pay and incentives., • We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs., • In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave., • Long-term equity awards granted at group level may also be part of your package., • Further details will be provided during the application process., • Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable., • A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. xohynlm Discover how you can join us in changing people's lives. #J-18808-Ljbffr

Experteer Overview As Fabrication Manager, you lead offshore structure fabrication to ensure safe, on-time, within-budget delivery aligning with contract and quality standards. You’ll supervise site teams, collaborate with the contractor, and drive HSE and QA/QC across activities. The role interfaces with project leadership to monitor progress, mitigate risks, and ensure compliant deliveries from fabrication to commissioning. You will shape execution strategies for offshore wind packages and large-scale EPC projects in a multinational setting. Compensaciones / Beneficios • Provide leadership and coordination for offshore structure fabrication, building strong relationships with the Contractor • Lead a team of supervisors and ensure cross-team coordination across fabrication activities • Ensure activities meet contractual obligations, schedule, cost targets, and quality objectives • Promote high HSE standards and adherence to site rules and procedures • Monitor supplier progress against program milestones and KPIs; report to project leadership • Identify risks, develop mitigation measures, and integrate into risk management • Take ownership of QA/QC topics related to fabrication and support EPC contract closure from QA/QC, HSE, and commercial perspectives • Assist in technical analysis and monitoring of variation orders and claims to ensure cost-effective decisions • Guide interface and stakeholder coordination for transition from fabrication to commissioning and/or Ou0026M • Provide accurate, timely progress reporting aligned with project requirements • Ensure reporting aligns with project expectations Responsabilidades • Bachelor/Master in Engineering or similar (minimum) • ≥10 years of relevant experience in a similar role • Fabrication oversight experience for offshore wind or large-scale oil u0026 gas projects • International site management experience with EPC contractors • Project management training • Knowledge of FIDIC Contracts and INCOTERMS • Experience in fabrication and testing offshore structures (DNV-ST-0145, DNV-OS-C401) • Safety management training (NEBOSH, VCA) and ISO 9001 / quality auditing knowledge • Excellent written and oral English; Spanish language skills valued Requisitos principales • flexible working hours • remote work policies • private medical insurance • life and accident insurance • wellness program • professional development opportunities

Novartis is seeking an Associate Director to build and lead a Barcelona-based team for Clinical Data Analytics and Technology. You will guide a small agile team, connect with global colleagues, and turn strategic priorities into practical data, analytics, and technology solutions across clinical trial delivery. ¿Le interesa este puesto? Puede encontrar toda la información relevante en la descripción a continuación. The role emphasizes AI-driven innovation, risk-based quality management, xohynlm and compliance with GxP, GDPR, and data governance standards, with a mix of onsite and hybrid work at the #J-18808-Ljbffr

Who We Are: VEGA Chargers is a company specialising in the design and manufacturing of fast chargers (DC) for electric vehicles. At VEGA Chargers, we work tirelessly to create a more sustainable present and future in terms of mobility. To achieve this, we analyse our customers' needs and provide flexible and scalable charging solutions for electric vehicles. Our process starts from conceptualisation and design, leading to manufacturing and distribution. ⚡ What We Are Looking For: We are seeking an experienced Technical Services professional who specialises in electric-vehicle chargers. We are looking for someone passionate about enhancing the client experience, contributing to error prevention, and collaborating closely with the Product and R&D team. Your Responsibilities Will Include: Technical Support and Assistance: - Address customer inquiries, technical issues, and troubleshooting needs after a purchase, whether related to hardware, software, or electronic devices. - Provide support via phone, email, chat, or other channels to resolve customer concerns. Installation and Configuration: - Install, configure, and update software and hardware according to customer or company needs. - Ensure operating systems and applications are correctly installed and configured. Preventive and Corrective Maintenance: - Diagnose and repair defective equipment. - Provide preventive maintenance to avoid malfunctions or failures. - Perform on-site or remote technical services as needed. User Training: - Guide customers on proper product use and assist with common troubleshooting steps. Incident Management: - Log, classify, and track reported customer issues. - Prioritise problems based on urgency and impact. Monitoring and Analysis: - Supervise the condition of equipment and systems to identify potential failures before they occur. - Analyse recurring failure patterns to propose long-term solutions. Documentation and Reporting: - Maintain detailed records of service interventions and repairs. - Create technical reports on equipment status and applied solutions. Continuous Learning: - Stay updated on new technologies, products, and industry trends in technical support. Collaboration with Other Departments: - Logistics: Manage replacement parts delivery, returns, and repaired product shipments. - Product Development & Sales: Conduct surveys, collect customer feedback, and analyse it to identify product or service improvements. Requirements - Studies related to electrical or electronic engineering, mechatronics, automation, and industrial maintenance. - Computer skills, such as configuring a Local Area Network (LAN), configuring network interfaces, etc. Knowledge of object-oriented programming languages such as Python or Java will be highly valued. - Ability to interpret electrical diagrams and perform electrical troubleshooting. - Ability to communicate effectively in both Spanish and English. - Availability to travel sporadically. - Proven experience in After-Sales Services. - Hands-on experience with ticketing configuration and management. - Familiarity with OCPP protocols. - Passionate about enhancing the client experience and dedicated to error prevention. - Proven ability to collaborate and communicate effectively with various internal departments. - Strong analytical skills for reviewing and assessing potential clients. - Proficient in conducting maintenance remotely. - Alignment with the company's vision for creating a more sustainable future in terms of mobility. - Future availability for on-call duties will be required. - Demonstrates kindness and a positive attitude in interactions. Nice to have - Experience in the field of electric vehicle chargers. Benefits: - Coffee & Snacks ☕ - 22 days of holidays. - Be part of a team where your opinion matters, contributing to innovative creations. Selection process - Initial call with People: learn more about VEGA Chargers and introduce yourself. - Meeting with Jose (CPO) & Oriol (After Sales Manager). - Job Offer.

Experteer Overview In this role you will own the end-to-end delivery and evolution of a next-generation SaaS platform for study design, protocol authoring, and operational feasibility in clinical trials. You’ll bridge Ru0026amp;D business stakeholders, IT, and the vendor to drive design, testing, change management, and successful rollout. Post-launch, you’ll manage enhancements and adoption across a global matrix organization. This position sits at the crossroads of clinical operations, digital innovation, and enterprise IT, with a meaningful impact on patient-focused trials. Compensaciones / Beneficios • Lead solution design activities and translate business requirements into functional specifications • Support User Acceptance Testing (UAT) and facilitate alignment workshops • Drive change management and user onboarding for platform rollout • Manage lifecycle of the platform post go-live, including prioritizing enhancements and releases • Monitor performance and ensure sustainable adoption and business value realization • Collaborate with Ru0026D users, IT partners, and external software vendor • Contribute analytical expertise to broader digital Ru0026D initiatives in clinical trials Responsabilidades • 5+ years as IT Solution Lead, Application Lead, or similar in healthcare or life sciences • Deep knowledge of clinical trial processes, including protocol design and operational planning • Proven ability to translate complex business needs into functional specifications • Experience in regulated environments with software development lifecycle and CSV in line with GxP • Familiarity with clinical trial systems and data standards • Ability to navigate a global matrix organization and build trusted relationships across Ru0026D, IT, and external partners • Fluent in English; proactive, solution-oriented mindset Requisitos principales • diverse and inclusive culture • global opportunities • personal development and career advancement • flexible working culture • opportunity to impact patient outcomes • collaborative, innovative environment

ppbSalary Range: /b €63,600.00 - €118,000.00 /p p#LI-Hybrid /p pLocation: Barcelona, Spain /p pAs Associate Director - Clinical Data Analytics and Technology, you will help build and lead a new Barcelona-based team shaping the next generation of clinical data capabilities at Novartis. This is a frontline leadership role for someone with deep clinical research and clinical data operations experience who can translate between business, science, data, and technology — connecting clinical needs with analytics, automation, artificial intelligence, machine learning, risk-based quality management, and scalable data platforms. As part of the extended Clinical Data Analytics and Technology leadership group, you will guide a small, agile team, keep them closely connected to global colleagues, and turn strategic ideas into practical solutions that strengthen clinical trial delivery, data quality, operational efficiency, and decision-making for patients. This position is offered on a Hybrid working basis, with an expectation of 12 days per month onsite at our Barcelona Gran Via offices. /p h3Job Description /h3 h3Key Responsibilities /h3 ul liLead the transition to next-generation Clinical Data Operations capabilities by embedding analytics, automation, and digital innovation into core processes /li liDrive adoption of Artificial Intelligence-first strategies and emerging technologies to accelerate transformation and operational excellence /li liMentor and develop talent in clinical data analytics, Risk Based Quality Management (RbQM) and technology solutions /li liExecute the Clinical Data Operations Artificial Intelligence innovation strategy, translating strategic priorities into measurable business outcomes /li liLead cross-functional initiatives across Global Clinical Operations and Clinical Data Operations to advance company priorities and portfolio objectives /li liOversee end-to‑end Clinical Data Analytics and Technology activities, including analytics, reporting, visualization, risk-based quality management (RbQM), and technology implementation /li liDevelop innovative approaches for risk-based data review and monitoring, leveraging automation and Artificial Intelligence to improve quality, efficiency, and decision‑making /li liEnsure delivery of compliant, scalable, and secure solutions aligned with Good Clinical Practice, Good Practice requirements, General Data Protection Regulation, Health Insurance Portability and Accountability Act, and data governance standards /li /ul pLocation: Barcelona, Spain /p h3Essential Requirements /h3 ul liSignificant leadership experience within Clinical Data Operations, Clinical Data Management, Clinical Programming, or related clinical research environments, with a proven track record of building and developing high-performing teams /li liDeep understanding of clinical trial operations, clinical data review, Risk-Based Quality Management (RBQM), and the end-to‑end clinical data lifecycle, from data acquisition through monitoring, validation, reporting, and analysis /li liStrong knowledge of Artificial Intelligence (AI), Machine Learning (ML), automation technologies, cloud platforms, and business intelligence solutions, including Microsoft Power BI and Tableau, with experience applying these capabilities to clinical development or data-driven transformation initiatives /li liExperience working with modern clinical data technologies, including Electronic Data Capture (EDC) systems, Clinical Data Repositories (CDR), Statistical Computing Environments (SCE), and clinical reporting solutions such as J-Review /li liDemonstrated ability to translate clinical and business needs into analytics and technology strategies, influencing stakeholders across Clinical Data Operations, Data Science, Digital, and business functions to deliver measurable outcomes /li liFamiliarity with Clinical Data Interchange Standards Consortium (CDISC) standards, including Study Data Tabulation Model (SDTM), regulatory requirements, data governance principles, and Good Clinical Practice (GCP) and Good Practice (GxP) compliance frameworks /li liFluency in English, both written and verbal, is essential. /li /ul h3Benefits Rewards /h3 pAt Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. /p pbExpected Annual Base Salary Range for role: € /b63,600.00 - 118,000.00 /p pThe base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. /p pIn addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. /p pThe rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. /p pRead our brochure to learn more about our global total rewards offering: /p pNote: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. /p h3Commitment to Diversity and Inclusion / EEO paragraph /h3 pNovartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve. /p h3Skills Desired /h3 pClinical Studies, Clinical Trials, Data Analysis, Data Structures, Programming Languages, Statistical Analysis, Waterfall Model /p /p #J-18808-Ljbffr

Tecnoambiente busca un Data Centre Manager para su división Marine survey en España.La persona será responsable de la gestión de datos, entregables y reportes, asegurando que los proyectos se entreguen a tiempo, dentro del presupuesto y con los más altos estándares.Trabajará con colegas de di

Job Description Summary The Clinical Trial Excellence (CTE) Project Manager supports the delivery of operational excellence in trial management at Novartis, as defined by the CTE Head.Focusing on the Study Leader (SL) role, and associated ways of working, governance, collaboration, inspection readin

Novartis in Barcelona is seeking an Associate Director, Scientific Content (Neuroscience) to drive strategic planning and delivery of high-quality scientific and medical content across NS portfolio, aligning with international medical strategies and product lifecycle.You will oversee content develop

The Associate Director, Scientific Content (Neuroscience) is a strategic and execution-focused role within the International Medical Centre of Excellence (IMACE), accountable for supporting the planning, development, and delivery of high-quality scientific and medical content for the Neuroscience (N

Experteer Overview Join Grifols as IT Digital Technology Manager for Plasma Area, guiding the digital tech landscape that supports plasma donor centers. You will ensure reliable, secure, and compliant operations enabling safe, efficient collection activities. Lead strategic alignment, project delivery, and service excellence across plasma operations and IT partners. Collaborate with cross-functional teams to scale infrastructure and improve patient-centered outcomes. This role combines technical leadership with a mission-driven healthcare impact in a hybrid setup. Compensaciones / Beneficios • Domain management and strategic alignment for plasma donor centers • Lead plasma IT projects from planning to deployment and ensure cross-team coordination • Manage day-to-day service performance, incident handling, and deployment steps • Coordinate with CoC, MSP and vendors to meet SLAs and ensure production safety • Lead and develop the plasma IT team; maintain documentation and knowledge assets Responsabilidades • Bachelor in Computer Science, Telecommunications, or related field • Advanced English and Spanish communication skills • Minimum 5 years in plasma infrastructure environments including BECS systems and donor center infrastructure • Strong understanding of plasma-center technologies, IT frontend/backend, networking, monitoring • Knowledge of security, compliance practices, and regulatory requirements • Experience with ITSM frameworks (incident, change, release) and multi-vendor delivery (CoC, MSP) Requisitos principales • Hybrid work model • Benefits package

pNovartis Farmacéutica, S.A. in Barcelona invites an Associate Director, Scientific Content (Neuroscience) to lead strategic planning and execution of high‑quality scientific materials across NS portfolio, ensuring alignment with global objectives and regulatory standards. /ppThis role partners with IMACE, IMA and GMA teams, overseeing content development, governance, and lifecycle strategies, while guiding regional and country adaptations and driving timely delivery of scientifically robust /p #J-18808-Ljbffr

The Associate Director, Scientific Content (Neuroscience) is a strategic and execution‑focused role within the International Medical Centre of Excellence (IMACE), accountable for supporting the planning, development, and delivery of high‑quality scientific and medical content for the Neuroscienc

Novartis is seeking an Associate Director - IT Project Manager for Protective Security in Barcelona.The role leads end-to-end delivery of security IT initiatives across regions, aligning physical security with enterprise IT and regulatory requirements.Descubra exactamente qué habilidades, experienc

Tecnoambiente busca un Data Centre Manager para su división Marine survey en España. La persona será responsable de la gestión de datos, entregables y reportes, asegurando que los proyectos se entreguen a tiempo, dentro del presupuesto y con los más altos estándares. Trabajará con colegas de diferentes departamentos y liderará la planificación de procesos, flujos de datos y control de calidad, además de coordinar al equipo de procesamiento y comunicar avances al Project Manager. #J-18808-Ljbffr