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Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Radiometer, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. At Radiometer, life comes first. Our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses. We’re a team that celebrates diverse ideas and continuous improvement. Here, you’ll find a place to grow and make a real impact, with your unique perspective driving us forward in improving patient care. At Radiometer, our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses. We're seeking a Medical Information Advisor to join Radiometer's Global Medical Affairs team. This position drives critical medical and scientific initiatives both internally and externally, supporting our existing product portfolio while helping define the future of point-of-care technologies in acute and emergency healthcare environments. Based remotely in Spain with up to 25% travel to Copenhagen, Denmark, and various international locations. Part of our CMSS (Clinical, Medical Safety and Surveillance) Department, you'll report directly to our Senior Director of Medical Affairs. Your responsibilities will span leading medical initiatives across the organization, facilitating cross-functional collaboration in development projects, creating scientific and promotional materials, and building relationships with internal experts and Key External Experts (KEE) in hospitals globally. If you're energized by applying your medical and clinical expertise while engaging extensively with diverse stakeholders and are passionate about building an exceptional Medical Affairs organization, we'd love to hear from you. In this role, you will have the opportunity to: Lead Medical Information Strategy: Apply your Medical Affairs expertise to shape and execute the global medical information strategy, owning the development, quality, and lifecycle of scientific content and MAPSS assets while aligning cross-functional stakeholders on strategic priorities. Act as the Scientific and Clinical Expert: Serve as a trusted subject matter expert in acute and emergency diagnostics, translating complex clinical evidence into clear, actionable insights that inform Medical Affairs, Marketing, and product development decisions. Drive High-Impact Scientific Communications: Lead publication planning and execution, transforming clinical performance data into peer-reviewed evidence and compelling medical materials that strengthen scientific credibility and support global adoption. Build and Activate Global Expert Networks: Develop and manage strategic relationships with KOLs and KEEs, leading engagement processes, supporting IIS initiatives, and enabling high-value scientific collaborations that expand external impact. Represent Medical Affairs Internally and Externally: Play a visible role at scientific conferences and industry forums, delivering impactful presentations and ensuring consistent, compliant communication of medical insights across global stakeholders. The essential requirements of the job include: Advanced Credentials with Relevant Industry Experience: Hold an advanced degree in Life Sciences (PhD, PharmD, MSc, or equivalent) combined with a minimum of 5 years of experience in Medical Affairs, Medical Information, or related roles within the IVD, medical device, pharma or healthcare industry, with strong exposure to clinical applications. Strong Expertise in Medical Information and Processes: Demonstrate in-depth knowledge of medical information tools, processes, and compliance requirements, with hands-on experience developing, reviewing, and managing scientific and medical content in a regulated environment. Exceptional Scientific Communication Skills: Exhibit outstanding written and verbal communication in English, with proven ability to translate complex scientific data into clear, impactful messages for both expert and non-expert audiences. Solid Clinical and Technical Understanding: Bring strong familiarity with IVD technologies and their application in clinical settings, particularly in acute or hospital-based workflows, enabling meaningful scientific contribution and credible stakeholder engagement. Effective Cross-Functional Collaboration and Execution: Show the ability to work effectively across Medical Affairs, Clinical, Marketing, and external stakeholders, managing multiple priorities while maintaining high standards of quality, compliance, and execution. It would be a plus if you also possess previous experience in: Technical/Scientific knowledge /experience in Clinical Chemistry is desirable. Experience in Acute and Emergency care spaces is desirable At Radiometer, we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Radiometer can provide. #LI-Remote #LI-VF1 Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit _.

We are partnering with abr/br/leading multinational pharmaceutical company , internationally recognized for its scientific excellence, innovation, and global footprint, to find abr/br/P‑COR Leadbr/br/in Barcelona .br/br/This is abr/br/strategic and highly visible rolebr/br/within the organization, with responsibility for leadingbr/br/Clinical Outcome Assessment (COA)br/br/activities across a broad portfolio of therapeutic areas and ensuring a strongbr/br/patient‑centred approachbr/br/throughout the clinical development lifecycle. As P‑COR Lead, you will define and drive the global COA strategy, ensuring that clinical programs are informed by robust, validated, and meaningful outcomes that support both regulatory and commercial success. You will act as a key scientific and strategic partner to cross‑functional teams and external stakeholders.br/br/Key responsibilities include: Leading the development and execution of COA strategies across all therapeutic areas Advising clinical teams on the selection and implementation of appropriate COAs (PROs, ClinROs, eCOAs, etc.) Overseeing COA validation, psychometric analyses and scientific quality Leading COA projects end‑to‑end with vendors and internal stakeholders Collaborating with clinical, biostatistics, regulatory and data management teams Contributing to regulatory interactions, submissions and scientific communications Staying at the forefront of COA methodologies, standards and regulatory expectationsbr/br/Profile sought: MSc or PhD in Life Sciences, Psychology, Psychometrics, Biostatistics or related disciplines Minimum 3 - 5 years of experience in Health Outcomes Research, ideally within COA/PRO Strong knowledge of COA methodologies and global regulatory requirements Strategic mindset combined with scientific rigor Proven ability to influence, lead and collaborate in complex, matrixed environments High level of empathy and strong commitment to patient‑centred researchbr/br/What the company offers: A key leadership role within a global pharmaceutical organization High strategic impact and visibility Collaborative, international and cross‑functional environment Competitive compensation and benefits package Flexible working model with strong work‑life balance focusbr/br/

Experteer Overview As Senior Staff Software Engineer, you design and deliver features for Cloudera’s data engineering experience at scale, contributing to Spark and Livy while shaping the next generation of data tooling. You work with a distributed team across the US and Hungary to turn prototypes into production-grade capabilities that run on thousands of nodes. You’ll deepen expertise in distributed data processing and incubate improvements across the data engineering stack. This role offers the chance to impact enterprise-scale analytics in a hybrid, multi-cloud context. Compensaciones / Beneficios • Design and prototype new features for the data engineering experience, taking them through production delivery at scale • Contribute to Apache Spark and Livy development • Develop features in Scala/Java/Python on modern platforms • Gain and apply distributed data processing knowledge (SQL planners/optimizers, data layouts, Parquet/Iceberg, fault tolerance) • Develop deep understanding of the Cloudera Data Engineering Experience stack with a focus on Iceberg and Spark • Work on large-scale distributed systems in production clusters (hundreds to thousands of nodes) • Debug deployment issues, perform root-cause analysis, and conduct system test analysis • Improve internal infrastructure and collaborate with team members and stakeholders Responsabilidades • Bsc/Msc in related field or equivalent experience • 6+ years of professional software development • Experience leading and delivering complex product enhancements • Strong knowledge of Java/Scala/Python; able to work with at least one of these languages • Experience with distributed systems design and development • Strong communication skills; ability to research and solve problems independently • Open-minded with a willingness to learn and build great products • Experience with distributed systems Requisitos principales • Generous PTO Policy • Flexible WFH Policy • Continued Career Development • Comprehensive Benefits • Paid Volunteer Time • Unplugged Days

pAutodesk is seeking a Client Services Specialist in Barcelona to provide frontline support to customers and partners. You will troubleshoot access, licensing, and account issues while delivering an exceptional customer experience across multiple channels. /ppIdeal candidates have a BSc or MSc with 0–4 years of experience, CRM familiarity (Salesforce preferred), and flexibility for shift starts at 7:00 AM. Multilingual abilities are a plus in this fast‑paced role. /p #J-18808-Ljbffr

ph3Responsibilities /h3 ul liServe as a trusted advisor to onboard a portfolio of new clients and develop high-performing PPC campaigns for their digital marketing advertisement. /li liMake outbound customer calls to promote and sell services. /li liDetect and understand customer’s objectives and offer adapted solutions for their needs. /li liSet up strategic, results-driven campaigns designed for immediate impact and long-term performance sustainability. /li liBe responsible for increasing spend and campaign´s upselling. /li liCreate, maintain, and update a customer database with complete information. /li liHandle a high volume of potential clients daily through phone calls. /li /ul h3Requirements /h3 ul liBA/BS degree (MA/MSc in Marketing or Communications preferred) /li liLanguage Skills: C2 level of Dutch and C1 level of English (French is a plus). /li li20 months of experience in sales and/or marketing: previous client-facing experience, particularly in high-stakes environments. /li liAble to work independently and meet goals with occasional supervision. /li liFamiliar with managing customer data and using CRM tools to support business processes. /li liUses AI tools to support daily tasks and improve outreach strategies. /li liCommunicates clearly and effectively with different audiences. /li liComfortable working toward goals in a collaborative environment. /li liConfident in delivering presentations and writing professional content. /li liTakes initiative and maintains a proactive, solution-oriented attitude. /li liWorks well independently and contributes to team efforts /li liUnderstands business goals and supports strategic planning. /li liCapable of analyzing competitors and identifying trends to support positioning. /li liFocused on customer satisfaction and providing helpful support. /li /ul h3Certifications Qualifications /h3 ul liBA/BS degree /li liMA/MSc in Marketing /li liMA/MSc in Communications /li /ul /p #J-18808-Ljbffr

pAutodesk, Inc. is seeking a Client Services Specialist in Barcelona. This role involves providing frontline support, ensuring timely resolution of customer issues related to product access, licensing, and accounts. /ppIdeal candidates will have a BSc or MSc and fluency in both German and English, alongside experience in CRM systems. The position epitomizes a dynamic team environment and offers opportunities for professional growth. /p #J-18808-Ljbffr

A leading international bioanalytical organization is seeking a Pharmacokinetic Scientist in Barcelona. The role involves acting as Principal Investigator on studies, coordinating pharmacokinetic activities, and ensuring compliance with regulatory standards. Candidates should have an MSc or PhD in a relevant life science, strong expertise in Phoenix WinNonlin, and be fluent in English. This position offers high visibility in scientific projects and opportunities for growth in a collaborative international environment.br#J-18808-Ljbffr

A progressive bioanalytical CRO in Barcelona is seeking a Senior Scientist to coordinate analytical method validation and manage bioanalytical projects. The ideal candidate will have a PhD, MSc, or BSc in biology and a minimum of 3 years' experience in bioanalytical CROs, with solid skills in ELISA and MSD. This role offers a unique opportunity to work in a cutting-edge laboratory while contributing to the company's growth in an international environment.br#J-18808-Ljbffr

ph3Associate Principal, Implementation Science Mixed Methods Research /h3 pIQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward. /p h3Patient Centered Solutions (PCS) /h3 pThe Patient Centered Solutions (PCS) team leads the industry in the science of measuring the patient and stakeholder experience. PCS combines strategic consulting expertise with rigorous scientific methods to design and execute mixed‑methods, survey‑based, and implementation science research that informs development, access, and real‑world use of medical products and healthcare interventions. /p h3Why join? /h3 ul liBecome part of a recognized global leader in patient‑focused research /li liKeep growing with an organization that encourages and invests in continuous professional and personal development /li liApply your business and leadership skills in an entrepreneurial and multi‑disciplinary team /li liContinue challenging yourself by addressing the toughest client issues, working across multiple geographies and solutions in a dynamic and crucial field for the industry /li liMake a difference to patients by enabling the successful approval or launch of new treatments with features that are truly patient‑centric /li /ul h3Role Overview /h3 pAssociate Principal will serve as a senior subject matter expert in mixed‑methods research, survey science, and implementation science, supporting client delivery, business development, external thought leadership, and internal capacity building across the organization. This role emphasizes hands‑on scientific leadership, project delivery excellence, and growing external visibility. /p h3Key Responsibilities /h3 h3Client Delivery Scientific Leadership /h3 ul liServe as a senior scientific contributor and subject matter expert on client projects involving mixed‑methods research, survey studies, and implementation science methodologies. /li liLead or co‑lead study design, instrument development, qualitative and quantitative analysis, and interpretation of findings. /li liEnsure methodological rigor, alignment with best practices, and fit‑for‑purpose study designs across therapeutic areas. /li liReview and contribute to key scientific deliverables including protocols, analysis plans, reports, manuscripts, and client presentations. /li /ul h3Survey Science Mixed‑Methods Expertise /h3 ul liProvide expertise in survey design, item development, response scaling, cognitive testing, and item reduction. /li liApply mixed‑methods approaches to integrate qualitative and quantitative findings in a coherent and decision‑oriented manner. /li liSupport development and refinement of implementation‑focused measures, including barriers, facilitators, and outcome constructs. /li /ul h3Implementation Science Application /h3 ul liApply implementation science frameworks (e.g., CFIR, TDF, RE‑AIM) to inform study design, analysis, and interpretation. /li liSupport pragmatic and real‑world research intended to inform adoption, scale‑up, and sustainability of healthcare interventions. /li liTranslate implementation science concepts into actionable insights for clients. /li /ul h3Business Development Support /h3 ul liContribute to proposal development through methodological input, study design, and drafting of scientific sections. /li liParticipate in client meetings and presentations as a scientific subject matter expert. /li liSupport development of reusable methods, templates, and best practices that enhance proposal quality and efficiency. /li /ul h3External Thought Leadership /h3 ul liContribute to external visibility through conference abstracts, posters, presentations, and peer‑reviewed publications. /li liRepresent IQVIA as a credible scientific expert in mixed methods and implementation science under guidance of senior leadership. /li liParticipate in industry working groups, advisory boards, or collaborative initiatives as appropriate. /li /ul h3Internal Capability Building Mentorship /h3 ul liMentor junior and mid‑level staff on study design, analysis, and scientific writing. /li liSupport internal training initiatives, methods development, and communities of practice. /li liContribute to quality review processes and continuous improvement of scientific standards. /li /ul h3Qualifications Experience /h3 ul liAdvanced degree (PhD, DrPH, MD, PharmD, MSc, or equivalent) in a relevant scientific discipline strongly preferred. /li liDemonstrated expertise in mixed‑methods research, qualitative methods, and survey‑based research. /li liApplied experience using implementation science frameworks in healthcare or life sciences research. /li liStrong scientific writing and presentation skills, with experience contributing to client‑facing and external materials. /li liExperience working in a consulting or client‑facing research environment preferred. /li liAbility to independently lead multiple projects as a subject matter expert and collaborate effectively across multidisciplinary teams. /li /ul /p #J-18808-Ljbffr

ph3Overview /h3pEn este rol, serás Planning Analyst dentro de Accenture, impulsando transformaciones de la cadena de suministro para clientes de alto perfil. Trabajarás en un equipo altamente especializado, combinando trabajo en sitio con oportunidades locales, para entregar resultados tangibles mediante metodologías ágiles. Contribuirás a estrategias y modelos operativos que conectan planificación, compras, diseño de productos y cumplimiento. Buscamos a alguien proactivo, orientado a resultados y capaz de colaborar con múltiples partes interesadas para generar valor sostenible. /ph3Compensaciones / Beneficios /h3ulliImpulsar y apoyar transformaciones de cadena de suministro de extremo a extremo conforme a los desafíos del cliente /liliDefinir, optimizar e implementar procesos y modelos de operación de planificación de suministro de productos y servicios /liliTraducir requisitos funcionales y prioridades de stakeholders a equipos de integración de sistemas /liliPlanificar y monitorizar actividades de implementación para lograr resultados en plazo /liliDemostrar conocimiento de procesos de planificación de la cadena de suministro y sistemas asociados /liliAprovechar activos y metodologías de Accenture (ágiles) para acelerar y gestionar transformaciones /li /ulh3Responsabilidades /h3ulliExperiencia mínima de 1 año en consultoría (preferible) /liliExperiencia de al menos 1 año en cadena de suministro de servicios /liliExperiencia deseada con herramientas de planificación como IBP (SAP), OMP, o9, Kinaxis, Servigistics, Anaplan /liliDisposición para certificarse en una o más de las soluciones mencionadas /liliBuenas habilidades de comunicación y gestión de stakeholders /liliCapacidad para trabajar de forma creativa y analítica en entornos de resolución de problemas /liliInterés en entorno de consultoría estratégica con exposición a sistemas de información /liliAlta flexibilidad y organización para cubrir múltiples proyectos y clientes /li /ulh3Requisitos Principales /h3pEducación: Bachelor; preferible en Business (BBA o Economía) o ingeniería; inglés avanzado; postgrado deseable (MBA, MSc, Lean Six Sigma) /p /p #J-18808-Ljbffr

pSomma is hiring a Research Support Technician in Barcelona to focus on nanofabrication and nanoscale thermal transport. The technician will develop and study 2D materials, contributing to innovative research projects. /ppThis full-time position is suitable for candidates with a BSc/MSc in Physics, Nanoscience, or similar and involves excellent organizational and communication skills. Salary and relocation support are offered. /p #J-18808-Ljbffr

Pangea Propulsion is dedicated to developing advanced propulsion systems for the space industry based on the principles of high efficiency, sustainability, and reusability. We are revolutionizing the industry with groundbreaking innovations and aim to be the propulsion provider of the next generation of spacecraft. This role is a Turbomachinery Mechanical Design Engineer based in Barcelona, directly impacting the design and development of Pangea’s aerospike engine and other advanced rocket engines. The position requires leadership, creativity, innovation, and autonomy. • Design and develop turbine pump components such as pumps, turbine rotors, casings, seals, and bearings with a focus on performance, reliability, and manufacturability., • Lead the creation of detailed 3D models, technical drawings, and GD&T‑compliant documentation using CAD tools (preferably Siemens NX)., • Prepare comprehensive technical documentation, including design justifications, technical specifications, and assembly procedures., • Collaborate with fluidic engineers and analysts to iterate and improve designs based on test and simulation feedback., • Work with suppliers and internal manufacturing teams to ensure DfM compliance and component quality for both conventional and additive manufacturing methods., • Analyze test and simulation data to validate mechanical integrity and structural performance under thermomechanical loading., • Contribute to the continuous improvement of turbomachinery design practices and standards within the organization., • BSc in Mechanical Engineering, Aerospace Engineering, or a related field., • 5+ years of mechanical design experience in aerospace, turbomachinery, or related rotating equipment industries., • Proficient in 3D CAD design (Siemens NX preferred) and capable of working with complex assemblies., • Familiarity with PLM tools (preferably Teamcenter)., • Experience with ISO GPS standards and generation of detailed, production‑ready design drawings., • Solid understanding of thermomechanical loading, stress analysis, and rotor dynamics., • Familiarity with DfM principles for both conventional and additive manufacturing processes., • Working proficiency in English (Spanish and French are a plus)., • Curiosity, creativity, and passion for advanced propulsion technologies., • Analytical mindset with strong problem‑solving abilities., • Autonomy and ownership in delivering results under tight timelines., • Excellent communication and teamwork skills in multidisciplinary environments., • MSc in Mechanical Engineering, Aerospace Engineering, or a related field., • Background in rocket turbomachinery systems or liquid rocket engine components., • Experience with FEM tools (Ansys or Abaqus) for static and dynamic analysis., • Experience with programming and automation (Python or MATLAB)., • Knowledge of bearing and seal design principles for high‑speed rotating machinery., • Experience with combustion systems or rocket engine cycles., • Familiarity with aerospace standards for rotating or pressurized components. Pangea Propulsion is an equal‑opportunity employer committed to diversity and inclusion. We consider all applications without discrimination on any legally protected grounds and welcome applicants with disabilities, providing reasonable accommodations throughout the recruitment process and in the workplace. #J-18808-Ljbffr

ph3Senior Scientist (Study Director) – Large Molecule Bioanalysis /h3 pBarcelona, Spain /p h3Main Duties Responsibilities /h3 ul liCoordinate the validation of analytical methods to quantify drugs, anti-drug antibodies or biomarkers in biological matrices by ligand binding assays (ELISA, MSD) cell-based assays according to international guidelines. /li liCoordinate sample analysis projects, including regulated and non-regulated, pre-clinical and clinical studies. /li liDeliver extensive and effective communication with sponsors and timely delivery of results. /li liOrganize and line-manage laboratory personnel. /li liEffectively resolve technical and regulatory issues. /li liActively support Senior Management and participate in strategic projects to optimize procedures. /li /ul h3Required Profile Qualifications /h3 ul liPhD, MSc or BSc in biology or related subject. /li liMinimum 3-years experience in bioanalytical CROs. /li liExperience working with ELISA, MSD or other Ligand Binding techniques. /li liExperience in managing validation and sample analysis projects for determination of Immunogenicity and PK for pre-clinical and clinical studies. /li liExcellent level of English (Spanish – nice to have). /li liExperience working with cell culture techniques and qPCR will be highly valued. /li liDeep understanding of international bioanalytical guidelines for PK and Immunogenicity assay validation, and experience working under GLP/GCP regulations. /li liExperience working with LIMS systems. /li /ul h3Other Required Skills /h3 ul liStrong communication and organization skills, and capacity to work in teams. /li liProactive and hands-on approach. /li liHigh level of motivation and enthusiastic personality. /li /ul h3What Is Offered /h3 ul liOpportunity to work and contribute to the success of an expanding CRO. /li liSolid scientific team with career growth opportunities. /li liCutting edge laboratory with the latest technology. /li liInternational and multicultural environment in company based in Barcelona. /li liDiligent, professional organization, with a human touch. /li /ul pApply for this Position /p /p #J-18808-Ljbffr

pGalderma is seeking a Technical Product Lead to drive the technical success of dermatology skincare products. In this role, you will ensure alignment between formulation, process capability, and quality. You will work on high-impact projects in a global environment, supporting regulatory submissions and leading complex investigations. /ppThe ideal candidate will possess an MSc or PhD and have over 8 years of experience in the pharma or biotech industries. Join us in Barcelona to make a meaningful difference in dermatology. /p #J-18808-Ljbffr

About the role We’re looking for a Senior AI Engineer with excellent software engineering fundamentals to build reliable, production‑grade AI products for complex, document‑heavy workflows. This is a hands‑on role for someone who has taken LLM applications beyond prototypes and into production. You’ll work across applied AI, backend engineering, data, evaluation and infrastructure, with significant ownership from architecture through to deployment and continuous improvement. We care about new technology, but we care more about building products that are accurate, secure, useful and trusted. What you’ll do Build and operate production applications using LLMs and related AI technologies. Develop document ingestion, extraction, retrieval and question‑answering systems. Build and improve RAG, semantic search, reranking, tool use and agentic workflows. Create evaluation systems covering retrieval quality, factuality and end‑to‑end performance. Design for citations, traceability, auditability and appropriate human oversight. Build the APIs, data pipelines and infrastructure needed to run AI products reliably at scale. Monitor quality, latency, cost and reliability, and address hallucinations and regressions. Work closely with product, regulatory and commercial teams to solve real customer problems. What we’re looking for Five or more years of professional engineering experience. Strong computer science and software engineering fundamentals. Hands‑on experience building and deploying production LLM applications. Experience with RAG, embeddings, vector search, reranking, structured extraction, evaluation and monitoring. Evidence of taking products from initial concept to reliable production use. Strong communication skills and the ability to work across technical and non‑technical teams. A track record of owning meaningful outcomes for real users. A BSc in Computer Science, Software Engineering or a related field is preferred. An MSc in AI, Machine Learning or Data Science is valuable, but strong engineering ability matters more than the exact degree title. Particularly relevant experience Experience in any of the following would be a strong advantage: Document intelligence, search or structured information extraction. Complex PDFs, tables, forms, OCR and source‑level citations. Healthcare, life sciences, pharmaceuticals or another regulated industry. Security, access controls, audit trails and data privacy. LLM evaluation, red teaming and human‑in‑the‑loop review. High‑growth startups or scale‑ups. How we work High agency is essential. You’ll be expected to identify important problems, make progress through ambiguity and take responsibility for outcomes, not simply complete assigned tasks. You’ll be a strong fit if you: Care deeply about the quality and impact of your work. Move quickly without compromising safety or reliability. Raise problems early and bring potential solutions. Communicate clearly, collaborate well and operate with low ego. Are intellectually curious, pragmatic and passionate about building useful products. Take ownership from initial idea through to production and iteration. #J-18808-Ljbffr

Experteer Overview In this role you will shape and lead the global medical information and scientific content strategy for Radiometer’s Medical Affairs efforts. You will serve as a clinical and scientific expert in acute and emergency diagnostics, translating evidence into clear guidance for internal teams and external partners. You will drive high-impact scientific communications, including publication planning, to support global adoption of our products. You will build and manage a network of external experts to extend scientific reach, while representing Medical Affairs at conferences and cross-functional forums. This position combines scientific depth with cross-functional influence to advance patient care Compensaciones / Beneficios • Lead the global medical information strategy and lifecycle of scientific content and MAPSS assets • Serve as Scientific and Clinical Expert on acute and emergency diagnostics • Drive publication planning and execution to generate peer-reviewed evidence • Build and manage relationships with KOLs and KEEs to enable high-value collaborations • Represent Medical Affairs at scientific conferences and industry forums, ensuring compliant communication Responsabilidades • Advanced degree in Life Sciences (PhD, PharmD, MSc, or equivalent) with ≥5 years in Medical Affairs, Medical Information, or related areas in IVD/medical devices/pharma/healthcare • In-depth knowledge of medical information tools, processes, and compliance in regulated environments • Outstanding written and verbal English communication; ability to translate complex data for diverse audiences • Strong clinical and technical understanding of IVD technologies and hospital-based workflows • Proven cross-functional collaboration across Medical Affairs, Clinical, Marketing, and external stakeholders Requisitos principales • remote work option • flexible work arrangements • global collaboration • opportunity to impact patient care

Datavant is seeking a meticulous Data Scientist (Privacy) in Barcelona to join our Privacy Science team. You will analyse large health datasets, assess re-identification risk, and communicate insights to stakeholders. The role emphasizes rigorous methods, experimentation, and reporting.You will bring MSc/PhD level training in a quantitative field, strong Python skills, and knowledge of privacy concepts. Familiarity with AWS and SQL is a plus; hybrid work in Gracia is offered.#J-18808-Ljbffr

pDatavant, a data collaboration platform, seeks a meticulous Data Scientist (Privacy) in Barcelona to assess re-identification risk and safeguard patient privacy across health data sharing. You’ll work within the Privacy Science team, contribute to research, and develop analytic methods on large health datasets. /ppIdeal candidates hold an MSc/PhD in a quantitative field, are proficient in Python, and can communicate findings to stakeholders. /p #J-18808-Ljbffr

Experteer Overview As a Material Scientist at Galderma, you will apply hands-on expertise to understand, characterize, and optimize materials used in products and packaging. You’ll work in a small, highly technical team within a regulated environment, driving science-based solutions and robust documentation. Your work supports cross-functional teams to ensure performance, compatibility, and quality across formulations and packaging. This is an opportunity to contribute to a bold dermatology leadership trajectory and scale innovative materials globally. Compensaciones / Beneficios • Analyze and characterize materials and their chemical composition and behavior • Understand interactions between raw materials and packaging (tubes, bottles, etc.) • Assess how supplier differences impact material performance and product quality • Investigate material-related issues and drive practical, science-based solutions • Collaborate with cross-functional teams across Product Science, MSu0026T, and Quality • Translate complex findings into clear technical documentation and presentations Responsabilidades • MSc or PhD in Material Science, Chemistry, or related field • 3-8+ years in pharma, biotech, cosmetics, or injectable/aesthetic products • Strong expertise in material characterization and analytical techniques • Deep understanding of material interactions and applied science • Hands-on mindset with strong problem-solving and critical-thinking skills • Excellent technical writing and presentation abilities • applied material science in regulated industries (pharma, aesthetics, cosmetics) Requisitos principales •

Morgan Philips is seeking a MSL – Barcelona for a leading multinational pharmaceutical company.Location: Barcelona (field-based)Territory: Northeast SpainTherapeutica Area: Nephrology and TransplantationThe purpose of this role is to provide field-based medical and scientific expertise, fostering scientific exchange and supporting informed healthcare decision-making within the assigned territory.The MSL will:Serve as a trusted scientific partner to healthcare professionals and key stakeholders across relevant disease areas.Build and maintain strong, credible relationships with leading experts, healthcare institutions, and other scientific stakeholders.Contribute to medical strategy through high-quality scientific exchange, medical education, and insight gathering.Identify, collect, and communicate actionable medical insights to support evidence generation and strategic planning.Support research initiatives, real-world evidence projects, registries, and investigator-sponsored research activities.Contribute to launch readiness activities through scientific stakeholder mapping, identification of unmet needs, and analysis of the healthcare environment.Collaborate cross-functionally to support the implementation of affiliate and regional medical objectives.Maintain a minimum of 60% field-based activity.Minimum Education and Experience RequirementsBachelor's degree in a life science, pharmacy, medicine, nursing, or other relevant scientific discipline.Advanced scientific or medical degree preferred (MD, PharmD, PhD, MSc, or equivalent).Minimum 5 years of experience in Medical Affairs within the pharmaceutical or biotechnology industry.Previous experience as a Medical Science Liaison (MSL) is strongly preferred.Experience working with hospital-based and specialist therapies.Experience supporting scientific exchange with healthcare professionals and key opinion leaders.Experience in launch readiness and/or pre-launch activities is desirable.Desirable therapeutic area expertise in Nephrology and/or Transplantation.Native Spanish speaker.Good command of English.Knowledge and SkillsStrong understanding of compliance requirements and the pharmaceutical healthcare environment.Experience working successfully in a matrix organization with a high level of autonomy.Ability to adapt to evolving priorities while maintaining strategic focus.Strong scientific and medical acumen, including critical appraisal, interpretation, synthesis, and communication of clinical data.Excellent presentation, communication, and stakeholder engagement skills.Proven ability to establish and maintain scientific partnerships with key external experts.Strong customer and stakeholder orientation.Excellent planning, prioritization, and organizational skills.Strong cross-functional collaboration skills and ability to influence without authority.Ability to generate insights and translate scientific information into actionable recommendations.

peJoventut, a junior consultancy association in Barcelona, is hosting the Innovation Quest (IQ), a 4-day competition for ESADE BBA and MSc students. Participants will work in teams to propose innovative solutions for real companies, attend workshops, and engage in teambuilding activities, all while enjoying Barcelona's vibrant culture. /ppThis opportunity emphasizes 'learning by doing' and aims to connect the business world with fresh ideas from aspiring consultants. /p #J-18808-Ljbffr

ph3Contract Medical Science Liaison (MSL) – Clinical Trials (Spain) /h3 pFreelance / Contract, Location: Spain. /p p¿Desplácese hacia abajo y descubra qué habilidades, experiencia y cualificaciones académicas se necesitan. No espere a enviar su solicitud después de leer esta descripción; se espera un gran volumen de candidaturas para esta oportunidad. /p pWe are supporting a global biopharmaceutical company in hiring a Contract Medical Science Liaison (MSL) to support Phase 3 clinical trials in Respiratory / Rare Disease across Spain. Spain is a key country for these studies, with a high number of active trial sites, and this role will be critical in ensuring strong site engagement, high‑quality data generation, and successful trial delivery. /p h3Responsibilities /h3 ul liSupport patient recruitment strategies and site performance /li /ul h3Qualifications /h3 ul liPrior experience as a Medical Science Liaison (MSL) /li liAdvanced degree (PharmD, PhD, MD, or MSc) /li liFluent Spanish and English (required) /li /ul h3About the Candidate /h3 pIf you're an experienced MSL with strong clinical trial expertise and enjoy working in a dynamic, field‑based scientific role, we'd love to hear from you. /p /p #J-18808-Ljbffr

pSyneos Health is seeking a Principal Biostatistician to lead biomarker data projects across multiple studies in a fully remote role. Ideal candidates will hold a PhD or MSc in a relevant field and possess strong knowledge of biomarker evaluation, particularly related to immunology and infections. /ppThe position requires excellent communication skills and the ability to work independently. Knowledge of statistical programming in R and Python is essential. This role offers an exciting opportunity to influence biomarker research in clinical studies across Europe. /p #J-18808-Ljbffr

pulliPart-time /li /ulh3Company Description /h3peJoventut is a junior consultancy association managed by ESADE Business School students, which aims to create a bridge between the academic world and the real companies. Created as a non-profit association in 1985 in Barcelona, the mission of the junior enterprise is to give ESADE students the possibility of working in consultancy projects, in order for them to develop their skills, to put into practice what they have been learning at school and to have a first contact with the business world; as well as to provide companies an innovative and young reality with the rigor and the methodology of ESADE. /ph3Job Description /h3pThe Innovation Quest (also referred as IQ) is a case competition organized by eJoventut, ESADE's junior enterprise. The IQ consists of a 4-day competition between college BBA and MSc students who will work in teams to propose innovative solutions to real cases of the participant companies. /ppMoreover, the event offers the opportunity to attend conferences and workshops about innovation and entrepreneurship and to teambuilding activities as well, not to mention the added value of Barcelona’s life and business culture. /ppRegarding our mission we want to keep promoting the personal and professional development of our students through real consultancy projects in the fourth edition of our event. /ppEmphasizing our lemma “learning by doing” we pretend to connect the real Businesses World with the Fresh Ideas of the future consultants from all around the world. /ph3Qualifications /h3ulliEnrolled as a Business Student in ESADE /liliTeam Player /liliAbility to Work Under Pressure /liliResults Oriented /liliInterest forConsultancy /liliPresentation Skills /liliNetworking Ability /li /ulh3Additional Information /h3pAll your information will be kept confidential according to EEO guidelines. /p /p #J-18808-Ljbffr

Experteer Overview As an Optimization Scientist, you design and build optimization engines to rapidly recover airline operations from disruption. You own the end-to-end disruption-recovery solver pipeline, from formulation to production code, impacting real-world flight operations. Collaborating with Solutions Experts and engineering teams, you evolve the product’s optimization capabilities and performance. This role blends math and engineering to improve automated decision-making in a global, diverse environment. Compensaciones / Beneficios • Own a disruption-recovery solver pipeline end-to-end from mathematical formulation to production code • Translate airline rules (crew legality, aircraft routing, passenger reaccommodation) into solver formulations • Validate solver solutions against real disruption cases with Solutions Experts • Manage solution quality and runtime KPIs, balancing quality and solve time • Extend solver capabilities and ship new optimization functionality as the product evolves • Collaborate with Back-End and Data Engineering teams to integrate solver outputs into the live product • Build deep airline-operations domain knowledge to improve formulations Responsabilidades • Strong foundation in mathematical optimization and operations research (LP, MIP, network flows, large-scale techniques, or metaheuristics) • Hands-on experience with solvers (Gurobi, CPLEX, SCIP) • Proficiency in Python and SQL; experience with Git and optimization libraries; production-ready code • Ability to translate complex business rules into algorithms • Experience at the intersection of math and engineering, bridging OR theory and production code • Self-directed with ability to ramp up domain knowledge independently • Detail-oriented with precision in debugging solver behavior • Systems thinking: understand how formulation choices affect end-to-end performance • Degree in Operations Research, Applied Mathematics, Computer Science, Industrial Engineering or related field; MSc/PhD a plus Requisitos principales • Flex Week: work from home up to 2 days/week • Flex Day • Flex-Location: up to 30 days a year to work from any location • Employee Wellbeing: EAP for you and dependents • Professional Development opportunities with world-class platforms • Competitive benefits

pMerantix is seeking a Client Services Specialist in Barcelona to provide exceptional support to Autodesk customers. Responsibilities include troubleshooting licensing issues and delivering a high-quality customer experience through multi-channel support. The ideal candidate will hold a BSc or MSc and possess fluency in both German and English. /ppThe role demands strong problem-solving skills and the ability to manage multiple priorities in a dynamic environment. Flexible shifts and overtime may be required. /p #J-18808-Ljbffr

Part-timeCompany Descriptione Joventut is a junior consultancy association managed by ESADE Business School students, which aims to create a bridge between the academic world and the real companies. Created as a non-profit association in 1985 in Barcelona, the mission of the junior enterprise is to give ESADE students the possibility of working in consultancy projects, in order for them to develop their skills, to put into practice what they have been learning at school and to have a first contact with the business world; as well as to provide companies an innovative and young reality with the rigor and the methodology of ESADE.Job DescriptionThe Innovation Quest (also referred as IQ) is a case competition organized by e Joventut, ESADE's junior enterprise. The IQ consists of a 4-day competition between college BBA and MSc students who will work in teams to propose innovative solutions to real cases of the participant companies.Moreover, the event offers the opportunity to attend conferences and workshops about innovation and entrepreneurship and to teambuilding activities as well, not to mention the added value of Barcelona’s life and business culture.Regarding our mission we want to keep promoting the personal and professional development of our students through real consultancy projects in the fourth edition of our event.Emphasizing our lemma “learning by doing” we pretend to connect the real Businesses World with the Fresh Ideas of the future consultants from all around the world.QualificationsEnrolled as a Business Student in ESADETeam PlayerAbility to Work Under PressureResults OrientedInterest for ConsultancyPresentation SkillsNetworking AbilityAdditional InformationAll your information will be kept confidential according to EEO guidelines.

Ready to be part of a dynamic team that's revolutionizing the 3 D printing industry? Imagine a work environment where your every contribution creates a ripple effect of innovation. If you're drawn to challenges, seek out the thrill of cutting‑edge projects, and thrive in a culture of autonomy, trust, and ownership, then this is more than just a job – it’s a passion‑fuelled journey. Join us in shaping the future of 3 D printing, where your skills will be the driving force behind our success. At Supernova, we’re not just innovators; we’re game‑changers. Weaim to produce end‑use parts at scale and cost by developing a complete industrial solution to unlock the power and benefits of Additive Manufacturing. We are 100% customer‑centered and aware that the value we are bringing is the ability to produce fully functional parts. We work with the conviction that excellence in science and engineering is the cornerstone of transformative change. In our relentless pursuit of excellence, we adopt a champion’s mindset, we take controlled risks, and we are constantly on the offense to get things done. As a Senior Materials Scientist at Supernova, you will lead the formulation of high‑viscosity UV‑curable materials, vital for our Viscous Lithographic Manufacturing (VLM) technology. You’ll spearhead the development of new resins, applying your extensive knowledge in chemistry to create innovative solutions. Your role involves conducting detailed characterization studies to understand and improve material properties like strength, flexibility, and curing speed. You will be the driving force behind material advancements, ensuring our products meet the highest standards of quality and performance. A significant part of your role will be to collaborate closely with engineering colleagues. You’ll work hand‑in‑hand with the rest of the Material team, as well as with Mechanical and Process peers from the Engineering and Printing team, ensuring that the materials you develop are seamlessly integrated into our printing systems. Your expertise will guide all the technical teams in optimizing printer performance and achieving the best possible results with the materials you develop. Key Responsibilities es: Formulate, develop, and optimize industrial‑grade UV‑curable materials for 3 D printing applicatio ns. Bring your formulation expertise to perform state‑of‑the‑art research on the field of UV‑curable materia ls. Conduct rigorous laboratory experiments to evaluate new resin formulatio ns. Analyse and characterize material properties to ensure optimal performance and quali ty. Collaborate with the definition and implementation of laboratory best‑practices and H&S protoco ls. Collaborate with R&D teams to integrate new materials with printing syste ms. Lead initiatives to improve material properties, such as durability, flexibility, and curing spe ed. Guide and mentor lab technicians and interns, setting direction for day‑to‑day experimental w Qualifications You Ph D in Chemistry, Polymer Science, Materials Science or a related field— or an MSc/degree with extensive industrial formulation experience in coatings, adhesives, or other reactive/UV‑curable material systems tems Extensive hands‑on lab experience formulating and testing liquid or reactive material systems (photopolymer, thermoset, acrylic, urethane, or simil ar). Strong grasp of crosslinking/curing chemistry and structure–property relationships; direct photopolymerization experience is a plus but not requi red. Proven track record of innovative, hands‑on formulation or research w ork. Comfort working with high‑viscosity or high‑solids systems (or a strong rheology background) is an advant age. Strong problem‑solving skills and meticulous attention to det ail. Ability to work collaboratively in a dynamic R&D environm ent. Fluent in English, both in technical communication and documentat Why Supernova? Innovate at the Forefront: Drive innovation in 3 D printing, shaping the future of the next generation of AM industrial solut Creative & Analytical Synergy: Thrive in an environment where creative problem‑solving meets analytical rigor, making a real impact in our pioneering proj Growth & Learning: Enjoy continuous professional development at the edge where engineering, science and manufacturing meet. Ownership & Accountability: Take ownership of your role and tasks, ensuring accountability in every aspect of your work to make a tangible im #J-18808-Ljbffr

ph3Senior Director, Global Strategic Alignment Cell Therapy Platform /h3 pJoin to apply for the bSenior Director, Global Strategic Alignment Cell Therapy Platform /b role at bAlexion Pharmaceuticals, Inc. /b /p pPosted: 23-Dec-2025 Closing: 11-Jan-2026 /p h3What You Will Do /h3 ul liLead the development and refinement of global strategic plans, collaborating with key stakeholders across functions and regions to translate corporate Cell Tx vision into actionable strategies, milestones, and initiatives worldwide. /li liDrive alignment of strategic priorities across functions and geographies to ensure coherence, proper resource allocation, and maximize synergies while minimizing redundancies. /li liBuild strong relationships with internal and external stakeholders, including Therapeutic Area (TA) Heads, DRS leadership, and other key players within the AZ Cell Tx environment. /li liDrive organizational change initiatives to support implementation of strategic priorities within the Cell Tx platform. /li liDevelop and manage change‑management strategies across DRS to communicate, implement, and manage adoption for successful execution. /li liMaintain an entrepreneurial mindset, routinely predicting, identifying, generating, and evaluating alternatives to barriers in the business to keep the portfolio progressing to plan. /li liDrive fiscal prudence while balancing operational effectiveness by pressure‑testing study budgets, minimizing spend, and crafting cost‑saving strategies, while building internal knowledge on clinical‑trial delivery. /li liLead cross‑functional and global business‑excellence initiatives to streamline or develop processes, speed execution, and remove barriers across DRS. /li liEnsure all approaches comply with legal, compliance, and regulatory requirements. /li /ul h3What You Will Need to Have /h3 ul liA degree in a science‑related field or business administration with a proven track record in pharma, biotech, or CROs (Ph.D., MSc, MBA, BSc). Experience with advanced therapies or complex clinical platforms is preferred. /li liExperience with cell‑therapy development or platform management is a plus. /li liMinimum of 10 years of managerial experience in Business Management, Alliance, Business Operations, or related roles within the pharmaceutical or healthcare industry. /li liDemonstrated experience operating across global, cross‑matrix environments. /li liExperience managing multiple projects, delivering high‑quality results in fast‑paced, time‑sensitive settings. /li liStrong analytical skills to synthesize complex information and derive actionable insights. /li liExcellent leadership and influencing skills, with experience leading cross‑functional teams and driving change in dynamic environments. /li liExceptional communication and presentation skills, conveying complex ideas to diverse audiences. /li liStrategic thinker with a results‑oriented mindset and passion for driving innovation and growth. /li /ul h3Working at Alexion /h3 pWe’re inspired to think differently and create better outcomes, honoring integrity and dedication to improving lives affected by rare diseases. Our culture emphasizes an unparalleled employee experience, fostering a productive, engaging, and enjoyable workplace with world‑class leadership and innovation capabilities. /p h3The Highest Standards /h3 pWe operate with the highest ethical and integrity standards to earn trust from patients, physicians, and communities. /p h3Diversity /h3 pWe champion diversity in backgrounds and ideas, fostering an inclusive, high‑performing team that delivers extraordinary results. /p h3Dedication /h3 pOur employees’ dedication fuels our focus on medical innovation, redefining life with rare diseases. /p pThe role requires in‑office work 3 days a week, with flexibility balanced to respect individual needs. /p h3Equal Employment Opportunity /h3 pAlexion is proud to be an Equal Employment Opportunity and affirmative‑action employer, committed to inclusivity and fairness in all employment practices, and provides reasonable accommodations as needed. To discuss accommodations, contact Alexion participates in E‑Verify. /p /p #J-18808-Ljbffr

ppStrands is a leading bfintech /b company at the forefront of innovation in the financial industry. Our cutting-edge solutions empower banks and financial institutions to deliver personalized and intelligent banking experiences. Our products are fully embedded with Artificial Intelligence and Machine Learning capabilities so joining us is a great opportunity to be at the forefront of this new revolution. /p pSince 2020 we are part of the CRIF group, a world leader in the Financial Sector. So we have the best of both worlds, we operate as a startup and we are backed by a big company! /p h3ABOUT THE ROLE /h3 pWe are looking for passion, creativity, and commitment. /p pIf you are seeking for a mission-critical role where you get to combine your product management and software development expertise with business challenges, being a key member of our Barcelona Office, Strands is waiting for you! /p pAs a bProduct Owner /b, you will help to develop the product vision by working closely with Managers, C-level and stakeholders and execute such vision by cooperating with a team of talented engineers. /p h3YOU WILL BE DOING THINGS LIKE... /h3 ul liCreate and execute the vision for the product bringing together multi-disciplinary talented teams to deliver commercially viable and compelling products /li liOverseeing team projects removing blockers, ensuring project scope, and setting accurate timelines and deadlines /li liEnsures user stories, product ideas and improvements are ready for development to start work on it by providing strategic and hands‑on leadership to a strong multidisciplinary team /li liDefine Acceptance Criteria to validate product developments in order to define the optimal testing strategy to be executed by our Quality Assurance team /li liDocument product features and work closely with Marketing team to create sales collateral /li liDrive the release management process from the initial planning to the training of our Sales team /li liSet and review KPIs for the future improvements of our strategic development process /li liCreate or review product ideas to evaluate their inclusion in the product backlog /li liParticipate to pre‑sales activities, presentation of the solutions/products to prospect clients /li liEngage with customers (either directly or through the delivery team) in order to gain first‑hand knowledge of market feedback to develop valuable insights /li liAnticipate future product evolutions by keeping track of industry trends /li liLead market research processes to understand the requirements and user pains before building new features /li /ul h3YOU WILL BE USING YOUR... /h3 ul li5+ years of work experience. At least 1 year of experience in Product Management having a leading role /li liExperience from fast‑paced work environments such as fintech and/or startup /li liBSc. or MSc. in Engineering, Computer Science, Computer Engineering or other related fields /li liBalance of technical knowledge and business acumen /li liProven track record of delivering data‑driven solutions with a customer‑first mindset /li liEstablished background in launching software or services in partnership with engineering teams. High degree of proficiency in prototyping, iterative development, understanding of Agile principles /li liProactive, self‑starter with excellent project management skills and ability to manage multiple tasks effectively. Ability to prioritize effectively and get things done /li liExcellent communication skills with the ability to engage, influence, and inspire partners and stakeholders to drive collaboration and alignment /li liAbility to quickly create trust with both internal and external clients /li liHigh degree of organization, individual initiative, and personal accountability. Optimal analytical thinking and problem solving skills /li /ul h3YOU'LL LOVE IT BECAUSE YOU WILL GET... /h3 ul liOpportunities for professional growth and development; /li liA collaborative and supportive work environment; /li liGym free pass; /li liSubscription to unlimited online training courses by Udemy; /li liSnacks and food, Fresh organic fruit, drinks, tea, coffee and juices; /li liCutting‑edge technologies; /li liHybrid model of working from home and office attendance. /li liCompany tech sessions /li liSummer and Winter parties /li /ul pDon’t hesitate to apply even if you are not sure to cover all requirements, we would love to see your profile! /p /p #J-18808-Ljbffr

About the CompanyPlayvalve is a vibrant fast-growing gaming studio with an eye on the future. Our mission is to build fun and relaxing games meant to last, and we do that by bringing together a team of experts who love what they do. Our talented designers, artists, engineers, marketeers and analysts have created several games delivering joy and entertainment to over 20M users across more than 12 languages and 90 countries.About the RoleAs a Principal Applied Scientist, you’ll bridge rigorous science with production impact. This is not a pure engineering role, we need someone who thinks like a scientist first: formulating hypotheses, designing experiments with statistical rigor, and building models grounded in solid mathematical foundations. You’ll then work with Engineering to productionize these solutions at scale.You’ll own end-to-end problems in user behavior modeling, ad monetization optimization, and real-time decisioning systems. This means deep work on causal inference, probabilistic modeling, experimentation design, and optimization, not just applying off-the-shelf ML libraries. You’ll need to understand the ’why’ behind the models, not just the ’how.’We’re looking for someone who holds an advanced degree in a quantitative field, and has battle-tested their science in production environments. You should be equally comfortable working through the math behind a model as you are debugging production pipelines.Key ResponsibilitiesScientific Leadership & Problem Framing (50%)- Frame ambiguous business problems as well-defined scientific questions with testable hypotheses.- Design and analyze controlled experiments (A/B tests, multi-armed bandits) with proper statistical rigor.- Build probabilistic models for user behavior, lifetime value prediction, and ad response.- Apply causal inference techniques to untangle correlation from causation in observational data.- Stay current with research literature and bring cutting‑edge methods to production (when appropriate).Production ML Systems (20%)- Partner with Engineering to build real‑time decisioning APIs for game configuration and ad serving.- Implement proper monitoring, evaluation frameworks, and fallback mechanisms.- Ship models as stable services with clear performance guarantees.Experimentation & Measurement (20%)- Define success metrics and design experiments that provide unambiguous answers.- Build experimentation infrastructure and champion rigorous hypothesis testing across the org.- Quantify uncertainty and communicate statistical trade‑offs to non‑technical stakeholders.- Translate experimental results into business decisions with estimated impact.Strategic Collaboration & Mentorship (10%)- Work with Product, Marketing, and Ad Monetization to prioritize high‑impact projects.- Mentor other data scientists on scientific rigor.- Establish standards for model evaluation, code quality, and documentation.- Communicate complex technical concepts clearly to diverse audiences.Requirements- PhD or MSc in Computer Science, Statistics, Applied Mathematics, Physics, Operations Research, or closely related quantitative field.- 7+ years in data science with 2+ years owning production ML systems.- Expert‑level Python and SQL; comfortable writing production‑quality code.- Deep understanding of probability theory, statistical inference, and mathematical optimization.- Strong grasp of experimentation design and statistical hypothesis testing (power analysis, multiple testing corrections, variance reduction techniques).- Demonstrated ability to read, critique, and apply research papers to real‑world problems.Nice to have- Experience with modern ML frameworks (TensorFlow, PyTorch, JAX, or similar) for deep learning and/or probabilistic programming (e.G., PyMC, Stan, TensorFlow Probability).- Built and deployed end‑to‑end ML systems that handle millions of requests/predictions.- Proficiency with cloud platforms (GCP, AWS, Azure) for data processing and model serving.- Published research in top‑tier venues (NeurIPS, ICML, KDD, JMLR, etc.) or industry conferences.- Relevant Domain Experience (1‑2 of the following strongly preferred):- Gaming/mobile apps: LTV prediction, retention modeling, monetization optimization- Ad tech: Bidding strategies, auction mechanisms, ad serving optimization- Marketplace/platforms: Two‑sided market dynamics, pricing, recommendations.- Subscription/SaaS: Churn prediction, upsell optimization, cohort analysisWhat we offer- The Role: Own data science solutions from scratch with full autonomy. Join a meeting‑less company, no status updates, no sync calls, just deep work and results.- Location & Flexibility: Based in Barcelona (office with terrace, BBQ, beer tap). Flexibility policy: the data team comes in regularly because they want to, not because they have to.- Compensation & Perks: Competitive compensation based on experience, phantom stocks, relocation package, health insurance, ticket restaurant, unlimited vacations, regular company off‑sites.- The Challenge: 15 games in market + ambitious pipeline. Industry inflection point with AI and automation. Profit‑backed studio with no VC pressure and resources to do it right.#J-18808-Ljbffr

ph3Who We Are /h3 pNeuroelectrics is a creative, high‑tech company offering the best‑in‑class non‑invasive and high‑definition electrical brain stimulation technology for personalized neuromodulation. By measuring and modifying brain function, we aim to restore brain health, minimize disabilities and create a better life for patients. /p pWe are looking for new members of our team who already live by our shared values and are inspired by our company’s Vision — accelerate the evolution of brain science and technology by delivering advanced solutions to help end patients suffering from brain pathologies — and our Mission — revolutionize the understanding of the brain through new personalized neuromodulation therapies, anywhere and at any time. /p h3Position Summary /h3 pWe are looking for a Director of Engineering to own the full engineering function at Neuroelectrics — systems, hardware, firmware, software — and report to the Executive Committee as the senior technical voice in the company. Product decides what we build and for whom; you own how we build it: the architecture, the technical decisions, the engineering quality, and the team that ships it. You combine principal‑engineer‑level technical depth with proven leadership at scale. You are hands‑on by default — when a major signal‑integrity issue, a stubborn architectural question, or a release‑blocking bug shows up, you do not watch from the sidelines. /p pSystems, hardware and software engineering report to you. /p h3What Will You Do /h3 ul liContribute to company‑level strategy and decisions — from an engineering point of view — and put technical reality on the table when business calls are being made. /li liOwn the full engineering organization — systems, hardware, firmware, software — and the system‑level architecture that ties them together. Defend it when reality pushes back. /li liOwn engineering execution end‑to‑end: architecture, technical design, build quality, VV, release. Commit to feasibility, technical risk, capacity and schedule with eyes open, so Product can make scope and prioritization calls on solid ground. /li liBuild the engineering team. Hire and retain strong managers and senior Individual Contributors, develop the next layer of technical leaders, and shape an organization that matches where the product is going — not where it has been. /li liSet the engineering operating system: how we plan, how we review, how we ship. Design and code reviews, configuration management, test automation, release discipline. /li liBe the senior technical reference on the hardest problems: signal quality, stimulation delivery, connectivity, data integrity, firmware reliability, cloud uptime. You do not debug every issue — but when the team is stuck on something critical, you roll up your sleeves and engage at the same level as your strongest senior engineer. /li liOwn product reliability with Production and Customer Support: triage, complaint trending, corrective actions, reliability programs, and CAPA support when needed. /li liDrive platform modernization: pay down technical debt, modularize, and plan staged redesigns that lower risk while preserving compliance. /li liEmbed design controls and risk management into how engineering really works day to day; partner with RA/QA to keep traceability audit‑ready, not theatrical. /li liSet direction on hardware and firmware: low‑noise front‑ends, stimulation current sources and safety monitoring, wireless, EMC/ESD, DFM/DFT, production test. You don’t design the next board yourself, but you can challenge the people who do — in detail. /li liSet direction on software and cloud: device control applications, observability and telemetry, secure update strategy, cybersecurity for connected devices. You can review architectures and code with substance, not just slides. /li liWork as a peer with Product, RA/QA, Production, Clinical and Customer Support. Bring engineering reality into product and business decisions; once a decision is made, turn it into a rigorous technical plan your team can execute. /li /ul h3What Do You Need /h3 ul liBSc/MSc in Electrical/Electronics Engineering, Computer Engineering/Computer Science, Telecommunications, Physics, or a similarly rigorous quantitative field (or equivalent experience). /li liSignificant experience (typically 15+ years) across product and system engineering, including several years at director or head‑of‑engineering level with managers as direct reports. /li liDemonstrated track record building and growing engineering organizations: hiring strong people, developing managers, retaining technical talent, and shaping a culture where engineers do their best work. /li liTechnical depth at principal‑engineer level, applied at director scope — you own system‑level decisions across disciplines and have shipped products that customers depend on. /li liMedical device experience in regulated environments: design controls, risk management, VV, and tight collaboration with RA/QA. Familiar with ISO 13485, ISO 14971 and IEC 60601. /li liDeep electronics background is non‑negotiable: analog and mixed‑signal design, embedded systems and firmware, wireless, and EMC/ESD considerations. You can read schematics, engage seriously with PCB layout and BOM choices, and challenge designs at the level your hardware leads expect — or above. /li liSolid software engineering fundamentals — able to review architectures and major design decisions, not just project plans. Comfortable with automated testing and CI/CD as part of how engineering operates. /li liStructured root‑cause and reliability mindset: you build the systems and the team habits that close the loop from field issues to robust fixes. /li /ul h3Familiarity expected (or willingness to ramp quickly) /h3 ul liIEC 62304 (medical device software lifecycle) and IEC 62366‑1 (usability engineering). /li liIEC 60601‑1‑11 (home healthcare environment) for home‑use contexts. /li liCybersecurity for connected health devices and software (e.g., IEC 81001‑5‑1 principles). /li /ul h3Bonus points /h3 ul liBackground with EEG acquisition systems: biopotential front‑ends, electrode interfaces, artifact and noise mitigation. /li liBackground with tDCS/tACS/tRNS stimulators: current source design, compliance voltage, safety monitoring, isolation, stimulation protocols. /li liExperience leading engineering on cloud‑connected medical devices: telemetry, fleet management, remote updates, incident response. /li liExperience supporting EU MDR and/or FDA submissions — technical files, VV, audit interactions. /li liMSc/PhD in Biomedical Engineering, Neuroengineering or a related field. /li /ul h3Benefits /h3 ul liCompetitive salary in the sector (according to your experience/skills). /li li26 vacation days per year + 24th and 31th of December. /li liFully stocked kitchen (Coffee, organic fruits, snacks, and beverages). /li liFlexible Working Hours. /li liUp to 6 days of working from home per month. /li liPrivate Health insurance, including dental coverage. /li liProfessional development and collaborative environment. /li liUnique opportunity to join our company early with excellent market traction and huge potential to grow. /li liIncredible office in Barcelona in Av. Tibidabo. (shower, stunning views of all of Barcelona, etc.) /li liTeam Building Events. /li /ul /p #J-18808-Ljbffr

pPAL Robotics in Barcelona seeks a Robotics Engineer specialized in Reinforcement Learning to develop and validate policies for real robotic systems. This role bridges simulation and hardware, ensuring high reliability in robotic operations. /ppThe successful candidate will possess an MSc or PhD in a related field, along with strong expertise in Reinforcement Learning, deployment of policies on hardware, and proficiency in both Python and C++. We offer a flexible work environment including reduced hours to support work-life balance and a competitive salary package. /p #J-18808-Ljbffr

ph3PhD in Observational Cosmology at ICE-Barcelona /h3 pbLocation: /b Institute of Space Sciences (ICE-CSIC), Barcelona, Spain. /p pThe “Observational Cosmology and Extragalactic Astrophysics” group at the Institute of Space Sciences (ICE, CSIC; invites applications for one PhD position to start as early as September 2026. The candidate will work under the supervision of Dr. Martin Crocce and Dr. Matteo Zennaro. /p pbResponsibilities: /b The selected candidate is expected to research aspects of galaxy clustering and weak gravitational lensing, including their modeling through analytic theory or simulations and the cosmological inference. The student will contribute to the scientific exploitation of the ESA Euclid mission ( and other leading galaxy surveys, such as DESI, Rubin/LSST, and DES. /p pbGroup Overview: /b The host cosmology group covers a broad range of aspects in Observational Cosmology and the study of Large-Scale Structure, spanning theory modeling, production of simulations and mock catalogues, development of tools based on machine-learning and neural networks, and real data analysis. The group consists of 6 senior members, 4 research fellows, several postdocs and PhDs, and has access to computing facilities like the Marenostrum supercomputer, ICE cluster, PIC and CosmoHUB. /p pbQualifications: /b Applicants should have the academic credentials to enroll in the PhD program at the Autonomous University of Barcelona (UAB) during the 2026/2027 academic year. This typically requires having completed, or being close to completing, an MSc (Master) degree or equivalent. The position is for three years, with the possibility of an additional year extension. Salary and benefits are in line with other PhD positions in Spanish institutions. We encourage applicants from traditionally under‑represented groups in science, physics, and astronomy. /p pbApplication Details: /b Interested candidates should submit a short CV, academic transcripts, and one or two reference letters to Dr. Martin Crocce ( ) and Dr. Matteo Zennaro ( ). Use the email subject line “COSMOPHD” followed by the applicant’s surname(s). We encourage early applications before May 8, 2026, but the position will remain open until filled. For questions, contact the above emails. /p /p #J-18808-Ljbffr

pulliPart-time /li /ulh3Company Description /h3peJoventut is a junior consultancy association managed by ESADE Business School students, which aims to create a bridge between the academic world and the real companies. Created as a non-profit association in 1985 in Barcelona, the mission of the junior enterprise is to give ESADE students the possibility of working in consultancy projects, in order for them to develop their skills, to put into practice what they have been learning at school and to have a first contact with the business world; as well as to provide companies an innovative and young reality with the rigor and the methodology of ESADE. /ph3Job Description /h3pThe Innovation Quest (also referred as IQ) is a case competition organized by eJoventut, ESADE's junior enterprise. The IQ consists of a 4-day competition between college BBA and MSc students who will work in teams to propose innovative solutions to real cases of the participant companies. /ppMoreover, the event offers the opportunity to attend conferences and workshops about innovation and entrepreneurship and to teambuilding activities as well, not to mention the added value of Barcelona’s life and business culture. /ppRegarding our mission we want to keep promoting the personal and professional development of our students through real consultancy projects in the fourth edition of our event. /ppEmphasizing our lemma “learning by doing” we pretend to connect the real Businesses World with the Fresh Ideas of the future consultants from all around the world. /ph3Qualifications /h3ulliEnrolled as a Business Student in ESADE /liliTeam Player /liliAbility to Work Under Pressure /liliResults Oriented /liliInterest forConsultancy /liliPresentation Skills /liliNetworking Ability /li /ulh3Additional Information /h3pAll your information will be kept confidential according to EEO guidelines. /p /p #J-18808-Ljbffr

ppAistech Space is a dynamic-growing company focused on generating affordable, recurrent, high resolution thermal imagery of the planet to provide a new perspective of Earth’s changing resources. The company is based in Barcelona and aims to revolutionize remote sensing for environmental monitoring and resource management. /p h3What you will do /h3 pAistech Space is looking for a Satellite Systems Engineer to be part of the Space Infrastructure Team. The ideal candidate will bring systems engineering background and proven hands‑on expertise from Phase 0 through Phase E. /p pThis new position offers the opportunity to coordinate the interfacing between our ENABLER payloads with the new satellite platforms, as well as preparing the mission for daily operations in conjunction with the Ground and User infrastructure teams. /p pIn this role, you are expected to deal with the different Aistech departments, suppliers, clients, RD proposals, bureaucratic paperwork, launch plans and a long list of activities to push the company forward. /p pThe main responsibility for this job position is leading technically a heterogeneous team of engineers/scientists/sw developers to deliver the next ENABLER payloads into orbit and ensure the best geometric and radiometric performance of the ENABLER payloads producing high-quality imaging products. /p h3Key responsibilities /h3 ul liDefine mission CONOPS, system architectures, including computing system and subsystem budgets (power, data, link, pointing, etc.). /li liCapture, trace, and flow down mission‑level requirements to system and subsystem specifications. /li liPerform system engineering activities across all project phases, from preliminary design through to commissioning and operations. /li liPerform system‑level analysis, technical trade‑offs (cost, risk, schedule, performance), and manage the mission technical risk matrix. /li liPreparation of project documentation and presentation materials for all phases of the mission. /li liPlan and support Assembly, Integration, and Test (AIT) activities, including environmental testing, verification, and system validation. /li liSupport FMECA activities, and contribute to FDIR strategies. /li liAct as the primary technical interface for external stakeholders, supporting bid/tender activities, technical negotiations, and progress meetings. /li liPrepare, review, and maintain satellite mission models. /li liResearch of COTS technologies and solutions from the space industry. /li liDefine and maintain the mission technical schedule. /li liPropose new solutions to be applied into the company in order to improve processes and technologies at a business level. /li /ul h3Who you are /h3 h3Must /h3 ul liBSc/MSc in Aerospace, Telecommunications or relevant degree. /li liAt least 2 years of experience in satellite systems engineering. /li liProven experience in a full cycle of a satellite mission, from design phases until operations. /li liStrong knowledge of satellite subsystems: power, comms, AOCS, propulsion, EO payloads, etc. /li liExperience leading a team technically to deliver a payload into orbit. /li liExperience in systems engineering activities, covering requirements analysis, architecture design, AIT and VV processes. /li liExperience in environmental testing of space hardware (vibration, acoustic, shock, thermal vacuum, EMC). /li liKnowledge in orbital dynamics, RF analysis, system budgets, and end‑to‑end satellite and ground operations. /li liWork ethic: Independent, proactive and an active learner. /li liPersonality: Team player, extrovert and respectful with your colleagues. /li /ul h3Nice to have /h3 ul liExperience in any related projects with Thermal Payloads (MWIR, LWIR, etc). /li liExperience in STK, GMAT, MATLAB/SIMULINK or similar simulation SW packages. /li liGood knowledge of FMECA and FDIR design. /li liKnowledge of thermal design and FEM analysis of a payload or satellite system. /li liStrong knowledge of optical performance budgeting and optical geometric and radiometric calibration on‑ground and in‑orbit. /li liStrong knowledge developing code in Python. /li /ul h3What You’ll Gain by Joining Us /h3 ul liBe part of a passionate, collaborative, and respectful team. /li liEnjoy a stable, permanent contract with a fast‑growing company. /li liFlexible working hours and hybrid work: 6 days/month from home. /li liCompetitive salary and flexible retribution through Cobee. /li liFree access to paddle tennis courts and an on‑site gym. /li liDaily fresh fruit and coffee to keep you energized. /li liWork in an international, diverse environment. /li li23 vacation days, plus December 24 31, and birthday off. /li /ul /p #J-18808-Ljbffr

Experteer Overview As an MSL in Barcelona, you will provide field-based scientific expertise and foster trusted exchanges with healthcare professionals. You’ll shape medical strategy through credible education, insight gathering, and evidence generation across nephrology and transplantation. You will build and sustain expert relationships, support launch readiness, and collaborate with cross-functional teams to advance regional medical objectives. This role offers impact by translating science into practical guidance for decision-makers in a dynamic, regulated environment. Compensaciones / Beneficios • Provide field-based medical/scientific expertise and scientific exchange with professionals and stakeholders • Build and maintain credible relationships with leading experts, institutions, and key opinion leaders • Contribute to medical strategy through education, insight gathering, and evidence generation • Identify, collect and communicate actionable medical insights to support research and planning • Support research initiatives, real-world evidence projects, registries, and investigator-sponsored studies • Contribute to launch readiness through stakeholder mapping and identifying unmet medical needs • Collaborate cross-functionally to implement affiliate and regional medical objectives • Maintain at least 60% field-based activity Responsabilidades • Bachelor in Life Science (or related field) • Advanced scientific or medical degree preferred (MD, PharmD, PhD, MSc, or equivalent) • Minimum 5 years in Medical Affairs within pharma/biotech • Previous MSL experience strongly preferred • Experience with hospital-based and specialist therapies • Experience conducting scientific exchange with HCPs and KOLs • Launch readiness/pre-launch experience desirable • Desirable nephrology or transplantation expertise • Native Spanish; good English proficiency Requisitos principales •

ppAt Cloudera, we empower people to transform complex data into clear and actionable insights. With as much data under management as the hyperscalers, we're the preferred data partner for the top companies in almost every industry. Powered by the relentless innovation of the open source community, Cloudera advances digital transformation for the world’s largest enterprises. /p pbBusiness Area: /b ITbr/bSeniority Level: /b Mid-Senior level /p h3Staff IT Asset Architect you will /h3 ul liArchitectural Strategy: Lead the design and evolution of our asset and configuration management architecture within ServiceNow, ensuring it scales to cover all asset classes and supports both technical operations and business service visibility. /li liTaxonomy Governance Design: Define and own the enterprise asset tagging and metadata standards. Establish the policies that govern how assets are registered, classified, and decommissioned across business units, ensuring consistency from endpoint to cloud account. /li liStrategic Integration: Design and oversee integrations between ServiceNow and external systems including AWS, Azure, GCP, FinOps tooling, security scanners, and endpoint management platforms. Ensure a reliable, multi-source reconciliation model that keeps data accurate and current. /li liFull‑Spectrum Asset Lifecycle: Ensure end‑to‑end lifecycle visibility across all asset classes: physical endpoints, data centre hardware (compute nodes, switches, racks, cabling), cloud accounts and subscriptions, SaaS applications, and internal services. /li liCross‑Functional Leadership: Act as the primary bridge between Infrastructure, InfoSec, Finance, and Cloud Operations. Design the workflows, standards, and governance frameworks that these teams use to manage risk, control spend, and maintain compliance. You will lead through influence and expertise rather than direct authority. /li liAutomation Roadmap: Drive the organisation towards autonomous asset management. Design self‑healing workflows and automated discovery processes that reduce manual effort and proactively correct data quality issues. /li liService Mapping Dependency Visibility: Lead service mapping initiatives for critical applications, ensuring full visibility into upstream and downstream dependencies to support disaster recovery and business continuity planning. /li liExecutive Reporting CMDB Health: Develop KPIs and observability frameworks that communicate asset programme health, infrastructure risk, and financial exposure to VP and C‑suite stakeholders in clear business terms. /li /ul h3Required Experience /h3 ul liExperience: 7+ years in IT Infrastructure or IT Asset Management, with at least 3 years in a lead or architect capacity. Demonstrated experience operating across multiple asset domains, including physical infrastructure, cloud, and application portfolios. /li liEducation: Bsc/Msc in related field or equivalent experience. /li liGovernance Standards: Proven ability to design and enforce enterprise-wide asset governance frameworks, including tagging taxonomies, lifecycle policies, and data quality standards. /li liServiceNow: Strong hands‑on experience with the ServiceNow platform, including CMDB, Discovery, and Service Mapping capabilities. Familiarity with the Common Service Data Model (CSDM) and asset lifecycle management within ServiceNow is expected. Ability to work at a technical level with platform configuration and integration design. /li liCloud Modern Infrastructure: Solid understanding of multi‑cloud environments (AWS, Azure, GCP) and how cloud‑native resources, accounts, and subscriptions are managed as assets. Familiarity with containerised and episodic infrastructure. /li liIntegration Automation: Experience designing integrations between asset management platforms and external data sources. Comfortable working with APIs and automation tooling, with or without deep coding expertise. /li liCross‑Functional Influence: Demonstrated ability to drive adoption of standards and governance frameworks across teams where you hold influence rather than direct authority. Strong communication skills across technical and non‑technical audiences. /li liAnalytical Communication: Ability to translate complex infrastructure data into business risk and financial language for senior stakeholders. /li /ul h3Nice to Have /h3 ul liServiceNow Certified Implementation Specialist (CIS) in Discovery, Service Mapping, or Hardware Asset Management /li liITIL v4 Managing Professional or Strategic Leader /li liFinOps Certified Practitioner or equivalent cloud financial governance experience /li /ul h3Why Join Our Team? /h3 pAs a Staff Engineer, you are a technical sovereign. You will have the autonomy to dismantle legacy silos and build a world‑class asset intelligence platform. Your work will directly influence the company’s ability to scale, its posture against cyber threats, and its multi‑million dollar cloud efficiency strategy. /p h3What you can expect from us: /h3 ul liGenerous PTO Policy /li liSupport work life balance with Unplugged Days /li liFlexible WFH Policy /li liMental Physical Wellness programs /li liPhone and Internet Reimbursement program /li liAccess to Continued Career Development /li liComprehensive Benefits and Competitive Packages /li liPaid Volunteer Time /li liEmployee Resource Groups /li /ul pEEO/VEVRAA /p /p #J-18808-Ljbffr

Data Scientist (Privacy) Location: Barcelona, Spain Datavant is the data collaboration platform trusted for healthcare. Guided by our mission to make the world’s health data secure, accessible and actionable, we provide critical data solutions for organizations across the healthcare ecosystem - including providers, health plans, researchers, and life sciences companies. From fulfilling a single patient’s request for their medical records to powering the AI revolution in healthcare, Datavants are building the future of how data is connected and used to improve health. Datavant is looking for an enthusiastic and meticulous Data Scientist (Privacy) to join our growing team, which interrogates and assesses client information in terms of the re-identification risk to patients. As part of the Privacy Science team within Privacy Solutions you will play a crucial role in ensuring that privacy of patients is safeguarded in the modern world of data sharing. As well as working on real data, you will be involved in exciting research to keep us as industry leaders in this area, and stimulating discussions on re-identification risk. You will be supported in developing/consolidating data analysis and coding skills to become proficient in the analysis of large health-related datasets. You Will: Critically analyse large health datasets using standard and bespoke software libraries. Discuss your findings and progress with internal and external stakeholders. Produce high quality reports which summarise your findings. Contribute to research activities as we explore novel and established sources of re-identification risk. What You Will Bring to the Table: MSc or Ph D in Statistics, Mathematics, Physics, Chemistry or similar. Proficiency with programmable data analysis software Python, and the desire to develop expertise in its language. A good understanding of statistical probability distributions, bias, error and power as well as sampling and resampling methods. Seeks to understand real-world data in context rather than consider it in abstraction. Application of scientific methods to practical problems through experimental design, exploratory data analysis and hypothesis testing to reach robust conclusions. Strong time management skills and demonstrable experience of prioritising work to meet tight deadlines. Excellent communication skills. Meticulous attention to detail in the production of comprehensive, well-presented reports. Initiative and ability to independently explore and research novel topics and concepts as they arise, to expand Privacy Solution’s knowledge base. An appreciation of the need for effective methods in data privacy and security, and an awareness of the relevant legislation. Familiarity with Amazon Web Services cloud-based storage and computing facilities. Bonus: Experience with SQL. Bonus: Experience of creating documents using LATEX. Bonus: Detailed knowledge of one or more types of health information such as genomics. Bonus: Experience with public sector work. Perks of joining Datavant in Barcelona 25 vacation days Daily in-office lunch stipend (and a fully stocked kitchen) Hybrid work model: 2 days/ week in our office in Gracia Commitment to professional development opportunities Employee-led initiatives including annual company-wide innovation day & DEI resource groups Comprehensive private health coverage w/ out-of-network reimbursements options Flexible remuneration with Cobee (Restaurant, Transportation, Nursery) Peer & company recognition programs Monthly educational lunch & learns To ensure the safety of patients and staff, many of our clients require post-offer health screenings and proof and/or completion of various vaccinations such as the flu shot, Tdap, COVID-19, etc. Any requests to be exempted from these requirements will be reviewed by Datavant Human Resources and determined on a case‑by‑case basis. Depending on the state in which you will be working, exemptions may be available on the basis of disability, medical contraindications to the vaccine or any of its components, pregnancy or pregnancy‑related medical conditions, and/or religion. This job is not eligible for employment sponsorship. Datavant is committed to a work environment free from job discrimination. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. If you choose to respond, your answers will be anonymous and will help us identify areas for improvement in our recruitment process. #J-18808-Ljbffr

ph3Sr. Global Strategic Marketing Manager - Nutraceuticals /h3 pbLocation: /b Gava, B, ES, 08850 /p pbJob Type: /b Full-time, Hybrid /p pbTravel: /b Up to 25% globally /p h3How You’ll Make an Impact /h3 ul liDefine and lead the global strategic roadmap for nutraceutical actives, including segment prioritization and portfolio shaping /li liEstablish Lubrizol’s “right to win” through differentiated value propositions and targeted investment strategies /li liIdentify and unlock new growth platforms across applications, geographies, technologies, and partnerships /li liDrive disciplined portfolio management, balancing core optimization with next-generation innovation /li liLead forward-looking market intelligence to identify unmet needs, emerging trends, and structural growth opportunities /li liTranslate insights into actionable innovation pipelines, partnership strategies, and commercial playbooks /li liBuild robust, finance-aligned business cases with clear ROI and value capture mechanisms /li liOrchestrate cross-functional execution to bring innovation from concept to commercialization with speed and scalability /li liLead global marketing initiatives across commercial, business development, and technical teams to deliver above-market growth /li liRepresent Lubrizol externally with customers, industry bodies, and partners to strengthen thought leadership and positioning /li /ul h3Required Qualifications that Enable Your Success /h3 ul liBachelor’s degree in Business, Marketing, Life Sciences, or related field /li liMinimum 10 years of experience in strategic marketing, business leadership, or innovation-driven roles /li liProven track record of defining and executing global growth strategies /li liExperience within nutraceuticals, food, pharma, or adjacent regulated industries /li liStrong understanding of nutraceutical value chains, regulatory environments, and innovation ecosystems /li liDemonstrated ability to lead and influence cross-functional, global teams /li liStrong financial acumen with experience building investment cases and driving ROI /li liExcellent communication, stakeholder management, and strategic thinking skills /li /ul h3Preferred Qualifications that Drive You Forward /h3 ul liAdvanced degree (MBA, MSc, or PhD) in a relevant discipline /li liExperience working across multiple regions in a global organization /li liExposure to external innovation ecosystems, partnerships, or MA projects /li liExperience with commercialization of new technologies or ingredients /li /ul h3Work Environment /h3 ul liUse of computers and digital tools in a hybrid office environment /li liRegular collaboration with global, cross-functional teams /li liOccasional international travel for customer, partner, and industry engagement /li liAdherence to corporate policies, safety standards, and ethical guidelines /li /ul h3Benefits that Empower You /h3 ul liCompetitive salary with performance-based bonus plans /li liPaid holidays, vacation, and parental leave /li liFlexible work environment /li liLearning and development opportunities /li liCareer and professional growth /li liInclusive culture and global collaboration /li /ul /p #J-18808-Ljbffr

At Cloudera, we empower people to transform complex data into clear and actionable insights. With as much data under management as the hyperscalers, we're the preferred data partner for the top companies in almost every industry. Powered by the relentless innovation of the open source community, Cloudera advances digital transformation for the world’s largest enterprises. Business Area: ITSeniority Level: Mid-Senior level Staff IT Asset Architect you will Architectural Strategy: Lead the design and evolution of our asset and configuration management architecture within Service Now, ensuring it scales to cover all asset classes and supports both technical operations and business service visibility. Taxonomy & Governance Design: Define and own the enterprise asset tagging and metadata standards. Establish the policies that govern how assets are registered, classified, and decommissioned across business units, ensuring consistency from endpoint to cloud account. Strategic Integration: Design and oversee integrations between Service Now and external systems including AWS, Azure, GCP, Fin Ops tooling, security scanners, and endpoint management platforms. Ensure a reliable, multi-source reconciliation model that keeps data accurate and current. Full‑Spectrum Asset Lifecycle: Ensure end‑to‑end lifecycle visibility across all asset classes: physical endpoints, data centre hardware (compute nodes, switches, racks, cabling), cloud accounts and subscriptions, Saa S applications, and internal services. Cross‑Functional Leadership: Act as the primary bridge between Infrastructure, Info Sec, Finance, and Cloud Operations. Design the workflows, standards, and governance frameworks that these teams use to manage risk, control spend, and maintain compliance. You will lead through influence and expertise rather than direct authority. Automation Roadmap: Drive the organisation towards autonomous asset management. Design self‑healing workflows and automated discovery processes that reduce manual effort and proactively correct data quality issues. Service Mapping & Dependency Visibility: Lead service mapping initiatives for critical applications, ensuring full visibility into upstream and downstream dependencies to support disaster recovery and business continuity planning. Executive Reporting & CMDB Health: Develop KPIs and observability frameworks that communicate asset programme health, infrastructure risk, and financial exposure to VP and C‑suite stakeholders in clear business terms. Required Experience Experience: 7+ years in IT Infrastructure or IT Asset Management, with at least 3 years in a lead or architect capacity. Demonstrated experience operating across multiple asset domains, including physical infrastructure, cloud, and application portfolios. Education: Bsc/Msc in related field or equivalent experience. Governance & Standards: Proven ability to design and enforce enterprise-wide asset governance frameworks, including tagging taxonomies, lifecycle policies, and data quality standards. Service Now: Strong hands‑on experience with the Service Now platform, including CMDB, Discovery, and Service Mapping capabilities. Familiarity with the Common Service Data Model (CSDM) and asset lifecycle management within Service Now is expected. Ability to work at a technical level with platform configuration and integration design. Cloud & Modern Infrastructure: Solid understanding of multi‑cloud environments (AWS, Azure, GCP) and how cloud‑native resources, accounts, and subscriptions are managed as assets. Familiarity with containerised and episodic infrastructure. Integration & Automation: Experience designing integrations between asset management platforms and external data sources. Comfortable working with APIs and automation tooling, with or without deep coding expertise. Cross‑Functional Influence: Demonstrated ability to drive adoption of standards and governance frameworks across teams where you hold influence rather than direct authority. Strong communication skills across technical and non‑technical audiences. Analytical Communication: Ability to translate complex infrastructure data into business risk and financial language for senior stakeholders. Nice to Have Service Now Certified Implementation Specialist (CIS) in Discovery, Service Mapping, or Hardware Asset Management ITIL v4 Managing Professional or Strategic Leader Fin Ops Certified Practitioner or equivalent cloud financial governance experience Why Join Our Team? As a Staff Engineer, you are a technical sovereign. You will have the autonomy to dismantle legacy silos and build a world‑class asset intelligence platform. Your work will directly influence the company’s ability to scale, its posture against cyber threats, and its multi‑million dollar cloud efficiency strategy. What you can expect from us: Generous PTO Policy Support work life balance with Unplugged Days Flexible WFH Policy Mental & Physical Wellness programs Phone and Internet Reimbursement program Access to Continued Career Development Comprehensive Benefits and Competitive Packages Paid Volunteer Time Employee Resource Groups EEO/VEVRAA #J-18808-Ljbffr

ph3Key Responsibilities /h3 ul libClient Onboarding Advisory: /b Serve as a trusted advisor to onboard new clients, understanding their objectives to develop strategic, results-driven PPC campaigns for immediate impact and long-term sustainability. /li libSales Revenue Growth: /b Drive revenue growth by effectively selling and convincing clients through outbound calls; focus on increasing spend and campaign upselling. /li libMarket Engagement: /b Engage with the German market to detect customer needs, offering adapted solutions and identifying potential future unicorns. /li libAccount Database Management: /b Manage a high volume of accounts and potential clients daily, maintaining an updated customer database with complete and accurate information. /li libPerformance KPIs: /b Work consistently to meet or exceed performance targets and sales KPIs in a fast-paced environment. /li libRelationship Management: /b Cultivate long-term loyalty and satisfaction by building strong relationships with stakeholders and providing timely resolutions to inquiries. /li libStrategic Optimization: /b Quickly adapt to changing customer needs and business priorities, ensuring high-quality service and sales support. /li /ul h3Requirements /h3 ul libEducation: /b BA/BS degree and/or equivalent practical experience (MA/MSc in Marketing or Communications preferred). /li libLanguages: /b C2 level of German and a high level of English (both written and spoken). /li libExperience: /b Proven sales and/or marketing experience (2+ years preferred), with a track record of winning over clients in high-stakes, target-driven environments. /li libTechnical AI Savvy: /b Regularly integrates AI tools into workflows and interprets insights to personalize outreach; experienced in improving CRM systems. /li libGerman Market Expertise: /b Deep understanding of German business etiquette, cultural nuances, and regional digital marketing ecosystems. /li libRegulatory Knowledge: /b Awareness of local regulations, specifically GDPR and data privacy, to ensure compliant outreach. /li libCommunication Skills: /b Excellent written and verbal presentation skills; ability to persuasively explain complex ideas and handle sophisticated ROI questions. /li libResilience Mindset: /b Self-motivated, proactive, and resilient with the ability to work independently while collaborating actively with a team. /li libAnalytical Skills: /b Solid business acumen with the ability to conduct competitor analysis and analyze market trends to inform strategic positioning. /li /ul h3Benefits /h3 ul liA competitive 30.000€ salary: 26,000 base salary plus €4,000 in performance bonuses, including accelerators that let you earn beyond 100% when you exceed your targets. /li liFull‑time role (Monday to Friday) in a hybrid-working model /li liBoost your earnings with our Referral Program, offering up to €3,000 per successful hire. /li liRelocate smoothly with a flight‑included package and private studio accommodation (subject to availability). /liliEnjoy private health insurance. /li liGrow fast thanks to clear career paths, dedicated coaching, and a team that celebrates your success with continuous training and certifications that elevate your professional profile. /li liExperience a lively, engaging workplace at the World Trade Center Barcelona, surrounded by sea views and an inspiring atmosphere. /li /ul /p #J-18808-Ljbffr

ph3Overview /h3 pGNV (Grandi Navi Veloci), una empresa del Grupo MSC, es una de las navieras líderes en el mar Mediterráneo con una flota actual de 25 barcos que operan 33 líneas en 8 países. /p pCon el objetivo de reforzar nuestro bpersonal de taquilla durante la temporada alta de verano /b, abrimos vacante bTEMPORAL /b en nuestra sede de Barcelona. Jornada completa, en turnos rotativos. /p h3Responsibilities /h3 ul liGestionar la reserva, venta, anulación y sustitución de billetes a pasajeros; /li liComprobar la documentación de los pasajeros que viajan de acuerdo con las normativas legales vigentes, con especial referencia a los pasajeros residentes en Baleares; /li liAsistir al cliente y brindarle la información solicitada, ofreciendo un servicio de calidad; /li liGestionar un fondo de caja personal y ocuparse del cierre de caja con su correspondiente cuadre con las operaciones de cobro realizadas. /li /ul h3Qualifications /h3 ul liBachillerato. Valorable estudios superiores. /li liValorable experiencia previa de al menos 1 año en el sector turístico. /li liInglés nivel intermedio. Valorable segundo idioma. /li liBuen nivel de comunicación, gestión del tiempo y del estrés y fuerte orientación al cliente. /li /ul /p #J-18808-Ljbffr

Experteer Overview In this role you will lead electrical design for mission-critical data centres, guiding projects from concept to construction closeout. You will drive innovative, scalable electrical solutions and mentor a multidisciplinary design team to deliver high-quality outcomes. You’ll act as a client-facing technical lead, collaborating with project management, commercial, and construction teams. This position sits at the intersection of IT and facilities, helping Eaton respond to rapid data center growth driven by digitization and AI. You will shape design standards and pursue long-term innovation within a sustainability-focused, global company. Compensaciones / Beneficios • Act as Design Manager for data centre projects, leading electrical design from concept to closeout • Remain hands-on in electrical design and own critical design aspects • Lead and coordinate electrical engineers and SMEs within a multidisciplinary team • Manage design deliverables, resources, schedules, and quality across projects • Provide technical guidance and mentorship to the DC Design u0026 Engineering team • Develop and uphold electrical design standards, procedures, and best practices • Review and approve designs, calculations, reports, and specs; facilitate peer reviews • Serve as client-facing technical lead in meetings with clients, contractors, and Eaton • Lead value engineering, optioneering, and technical decision-making • Participate in site visits to monitor, review, and resolve electrical installation and commissioning matters • Collaborate with project management, commercial, and construction teams to ensure project success Responsabilidades • BSc / MSc in Electrical Engineering (MSc preferred) • 8-10 years of experience in electrical engineering for mission-critical facilities • Experience with MV and LV power distribution, transformers, UPS and standby generation • Strong knowledge of electrical codes, standards, and best practices • Experience with value engineering and integrating new technologies • AutoCAD and Revit knowledge advantageous • Fluent in Spanish and/or Italian u0026 English • Familiarity with edge computing and AI concepts • Strong analytical and problem-solving skills • Strategic thinking and ability to build teams and scalable processes Requisitos principales • Competitive compensation • Internal promotion opportunities • Eaton University learning and development • Challenging projects in dynamic team • Health and safety focus • Sustainability-focused culture

Datavant is the data collaboration platform trusted for healthcare. Guided by our mission to make the world’s health data secure, accessible and actionable, we provide critical data solutions for organizations across the healthcare ecosystem—including providers, health plans, researchers, and life sciences companies. From fulfilling a single patient’s request for their medical records to powering the AI revolution in healthcare, Datavanters are building the future of how data is connected and used to improve health. By joining Datavant today, you’re stepping onto a driven and highly collaborative team that is passionate about creating transformative change in healthcare. Datavant is looking for an enthusiastic and meticulous Data Scientist (Privacy) to join our growing team, which interrogates and assesses client information in terms of the re-identification risk to patients. As part of the Privacy Science team within Privacy Solutions you will play a crucial role in ensuring that privacy of patients is safeguarded in the modern world of data sharing. As well as working on real data, you will be involved in exciting research to keep us as industry leaders in this area, and stimulating discussions on re-identification risk. You will be supported in developing/consolidating data analysis and coding skills to become proficient in the analysis of large health-related datasets. You Will Critically analyse large health datasets using standard and bespoke software libraries. Discuss your findings and progress with internal and external stakeholders. Produce high quality reports which summarise your findings. Contribute to research activities as we explore novel and established sources of re-identification risk. What You Will Bring To The Table MSc or Ph D in Statistics, Mathematics, Physics, Chemistry or similar. Proficiency with programmable data analysis software Python, and the desire to develop expertise in its language. A good understanding of statistical probability distributions, bias, error and power as well as sampling and resampling methods. Seeks to understand real-world data in context rather than consider it in abstraction. Application of scientific methods to practical problems through experimental design, exploratory data analysis and hypothesis testing to reach robust conclusions. Strong time management skills and demonstrable experience of prioritising work to meet tight deadlines. Excellent communication skills. Meticulous attention to detail in the production of comprehensive, well-presented reports. Initiative and ability to independently explore and research novel topics and concepts as they arise, to expand Privacy Solution’ knowledge base. An appreciation of the need for effective methods in data privacy and security, and an awareness of the relevant legislation. Familiarity with Amazon Web Services cloud-based storage and computing facilities. Bonus: Experience with SQL. Bonus: Experience of creating documents using LATEX. Bonus: Detailed knowledge of one or more types of health information such as genomics. Bonus: Experience with public sector work. Perks of joining Datavant in Barcelona 25 vacation days Daily in-office lunch stipend (and a fully stocked kitchen) Hybrid work model: 2 days/ week in our office in Gracia Commitment to professional development opportunities Employee-led initiatives including annual company-wide innovation day & DEI resource groups Comprehensive private health coverage w/ out-of-network reimbursements options Flexible remuneration with Cobee (Restaurant, Transportation, Nursery) Peer & company recognition programs Monthly educational lunch & learns To ensure the safety of patients and staff, many of our clients require post-offer health screenings and proof and/or completion of various vaccinations such as the flu shot, Tdap, COVID-19, etc. Any requests to be exempted from these requirements will be reviewed by Datavant Human Resources and determined on a case‑by‑case basis. Depending on the state in which you will be working, exemptions may be available on the basis of disability, medical contraindications to the vaccine or any of its components, pregnancy or pregnancy‑related medical conditions, and/or religion. This job is not eligible for employment sponsorship. Datavant is committed to a work environment free from job discrimination. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. To learn more about our commitment, please review our EEO Commitment Statement here. Know Your Rights, explore the resources available through the EEOC for more information regarding your legal rights and protections. In addition, Datavant does not and will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay. At the end of this application, you will find a set of voluntary demographic questions. If you choose to respond, your answers will be anonymous and will help us identify areas for improvement in our recruitment process. (We can only see aggregate responses, not individual ones. In fact, we aren’t even able to see whether you’ve responded.) Responding is entirely optional and will not affect your application or hiring process in any way. Datavant is committed to working with and providing reasonable accommodations to individuals with physical and mental disabilities. If you need an accommodation while seeking employment, please request it here, by selecting the ‘Interview Accommodation Request’ category. You will need your requisition ID when submitting your request, you can find instructions for locating it here. Requests for reasonable accommodations will be reviewed on a case‑by‑case basis. For more information about how we collect and use your data, please review our Privacy Policy. #J-18808-Ljbffr

ppWe are scientists, doctors, techies and humanity lovers, with the mission of building neuroelectronic interfaces to cure brain disorders. INBRAIN harnesses the extraordinary material properties of Graphene, the world’s thinnest and nobel-prize winning material, to build safe, uninvasive and highly efficient neural solutions. Our mission is to decode and modulate neural networks to improve people's lives. /p pAs a bSr. /b bMechanical Engineer /b at INBRAIN you will lead the mechanical design and the development of an implantable component within the product while overseeing the different stages of the development. /p pbCurrently, we are looking for 2 Senior Mechanical Engineers. At least 1 of them /b should be focusing on development and design of bactive implantable medical devices (Class 3). /b /p pYou will be at the forefront of bringing advanced healthcare solutions to market, making a tangible difference in people´s lives worldwide. /p h3YOUR PROFILE /h3 h3Main responsibilities /h3 ul liLead the design, assembly, prototyping and of the mechanical components that are part of an implantable system in direct collaboration with the electronics, systems, quality and regulatory teams. /li liDesign for reliability, manufacture and test, including concept engineering, functional analysis, FEM analysis, and mechanical modelling. /li liDeliver detailed documentation of the device design (BOM, drawings, Specifications, test plan,…) compliant with ISO 13485 and ISO14971 design control requirements. /li liSupport and collaborate with external partners in the outsourced design, assembly and test of mechanical components that are part of an implantable electro‑mechanical system. /li liDefine test plans and methods to verify safety and mechanical performance of the device, in compliance with applicable standards and in collaboration with other teams. /li liDesign and build and perform, experimental and product system setups necessary to perform bench tests, characterization testing, integration, system testing. /li liCreate test plans to verify our mechanical designs from the product requirements. /li liInitiate and contribute to design, technical and milestone reviews. /li liUnderstand DFR/DFM/DFT (Design for Reliability, Design for Manufacturing and Design for Test), including concept engineering, modelling, analysis, sensitivity, and stress analysis. /li liWork intensively with Quality, Regulatory, Clinical and Project Management on the formal product development procedure, perform or collaborate in design and stage reviews. /li /ul h3Mandatory Qualifications and Soft skills /h3 ul liBSc or MSc in Mechanical Engineering with at least 5 years of work experience within MedTech industry with proven experience executing a full development cycle. /li liExperience in developing multidisciplinary medical devices. /li liMinimum of 2 years of leading a technical mechanical engineering aspect of a project. /li liStrong practical engineering background in mechanical engineering for commercial production. /li liFamiliar with electrical engineering, DFM, DFR and design methodologies and tools (e.g., Solidworks, PDM, etc.) /li liFamiliar with manufacturing processes such as design for assembly, design for test, pFMEA, etc. /li liAbility to manage projects mandated to external sub‑contractors and manufacturing. /li liFluency in English required (English is company language). /li liFast learner, self‑motivated and pro‑active individual able to work in the fast‑moving environment of a dynamic start‑up company. /li liA system‑thinking attitude identify areas of potential improvement and develop plans to address these; Team oriented, a sparring partner to colleagues in other disciplines. /li /ul h3Nice to have /h3 ul liPreferred to have solid experience in neuroscience with a strong interest in gaining a further understanding of this field. /li liStrong hands‑on skills, experience with machine shop tools. /li liExtensive experience with active implantable medical device development /li liPreferred to have experience in applying quality control for medical devices (ISO13485) or in a similar working environment in a tightly regulated industry (e.g., medical devices). /li liPreferred to have a solid understanding of Medical Risk Analysis. /liliPreferred to have detailed understanding of active implantable medical device development and application of its relevant standards /li /ul h3WHY US? /h3 pWe are looking for someone who Is ready to proactively bring new ideas to the team, push boundaries, and constantly look for innovation. At INBRAIN we believe in shared success and diverse ways of thinking, here you'll learn, grow, and advance in an innovative culture. /p h3WHAT CAN WE OFFER TO YOU? /h3 ul liA collaborative environment where innovative ideas flourish and teamwork drives us forward. At INBRAIN, we believe the power of collective intelligence is unique. You will be part of a team that thrives on open communication, knowledge sharing and mutual respect. /li liMeaningful Work Impact: Our projects are not only exciting and challenging but also have a positive impact on the industry and society as a whole. You'll be part of a team that strives to create meaningful change. /li liCutting‑Edge Technology Exposure: Joining us means immersing yourself in the latest technologies and innovative solutions. You'll have access to state‑of‑the‑art tools and resources, fostering continuous learning and keeping your skills relevant in a rapidly evolving industry. /li liCompetitive salary (according to your experience/skills) /li liPrivate Health Insurance /li liTraining bonus for professional development and access to Udemy platform /li li23 vacation days per year /li liChristmas week off /li /ul h3Applications must be submitted in English /h3 pAt INBRAIN, we're not just offering a job – we're inviting you to be part of a transformative journey, Are you ready to transform lives? Join us! /p pWe believe that a diverse and well‑balanced workforce drives innovation. At INBRAIN, we foster the inclusion of all people regardless of culture, age, gender, sexual orientation, identity and diverse abilities or any other status /p /p #J-18808-Ljbffr

Datavant is the data collaboration platform trusted for healthcare. Guided by our mission to make the world’s health data secure, accessible and actionable, we provide critical data solutions for organizations across the healthcare ecosystem - including providers, health plans, researchers, and life sciences companies. From fulfilling a single patient’s request for their medical records to powering the AI revolution in healthcare, Datavanters are building the future of how data is connected and used to improve health. By joining Datavant today, you’re stepping onto a driven and highly collaborative team that is passionate about creating transformative change in healthcare. Datavant is looking for an enthusiastic and meticulous Data Scientist (Privacy) to join our growing team, which interrogates and assesses client information in terms of the re-identification risk to patients. As part of the Privacy Science team within Privacy Solutions you will play a crucial role in ensuring that privacy of patients is safeguarded in the modern world of data sharing. As well as working on real data, you will be involved in exciting research to keep us as industry leaders in this area, and stimulating discussions on re-identification risk. You will be supported in developing/consolidating data analysis and coding skills to become proficient in the analysis of large health-related datasets. You Will: Critically analyse large health datasets using standard and bespoke software libraries. Discuss your findings and progress with internal and external stakeholders. Produce high quality reports which summarise your findings. Contribute to research activities as we explore novel and established sources of re-identification risk. What You Will Bring to the Table: MSc or Ph D in Statistics, Mathematics, Physics, Chemistry or similar. Proficiency with programmable data analysis software Python, and the desire to develop expertise in its language. A good understanding of statistical probability distributions, bias, error and power as well as sampling and resampling methods. Seeks to understand real-world data in context rather than consider it in abstraction. Application of scientific methods to practical problems through experimental design, exploratory data analysis and hypothesis testing to reach robust conclusions. Strong time management skills and demonstrable experience of prioritising work to meet tight deadlines. Excellent communication skills. Meticulous attention to detail in the production of comprehensive, well-presented reports. Initiative and ability to independently explore and research novel topics and concepts as they arise, to expand Privacy Solution’ knowledge base. An appreciation of the need for effective methods in data privacy and security, and an awareness of the relevant legislation. Familiarity with Amazon Web Services cloud-based storage and computing facilities. Bonus: Experience with SQL. Bonus: Experience of creating documents using LATEX. Bonus: Detailed knowledge of one or more types of health information such as genomics. Bonus: Experience with public sector work. Perks of joining Datavant in Barcelona 25 vacation days Daily in-office lunch stipend (and a fully stocked kitchen) Hybrid work model: 2 days/ week in our office in Gracia Commitment to professional development opportunities Employee-led initiatives including annual company-wide innovation day & DEI resource groups Comprehensive private health coverage w/ out-of-network reimbursements options Flexible remuneration with Cobee (Restaurant, Transportation, Nursery) Peer & company recognition programs Monthly educational lunch & learns To ensure the safety of patients and staff, many of our clients require post-offer health screenings and proof and/or completion of various vaccinations such as the flu shot, Tdap, COVID-19, etc. Any requests to be exempted from these requirements will be reviewed by Datavant Human Resources and determined on a case‑by‑case basis. Depending on the state in which you will be working, exemptions may be available on the basis of disability, medical contraindications to the vaccine or any of its components, pregnancy or pregnancy‑related medical conditions, and/or religion. This job is not eligible for employment sponsorship. Datavant is committed to a work environment free from job discrimination. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. To learn more about our commitment, please review our EEO Commitment Statement here. Know Your Rights, explore the resources available through the EEOC for more information regarding your legal rights and protections. In addition, Datavant does not and will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay. At the end of this application, you will find a set of voluntary demographic questions. If you choose to respond, your answers will be anonymous and will help us identify areas for improvement in our recruitment process. (We can only see aggregate responses, not individual ones. In fact, we aren’t even able to see whether you’ve responded.) Responding is entirely optional and will not affect your application or hiring process in any way. Datavant is committed to working with and providing reasonable accommodations to individuals with physical and mental disabilities. If you need an accommodation while seeking employment, please request it here, by selecting the ‘Interview Accommodation Request’ category. You will need your requisition ID when submitting your request, you can find instructions for locating it here. Requests for reasonable accommodations will be reviewed on a case‑by‑case basis. For more information about how we collect and use your data, please review our Privacy Policy. #J-18808-Ljbffr

h3Description /h3pemAre you a Google fan? Do you love Google products? Are you passionate about the web and new technology? If you are tech savvy, creative, outgoing, and willing to roll up your sleeves and get things done in a fast-paced, rapidly changing environment, we may have the perfect job for you! /embr/ /ppstrongOur client /strong is a worldwide leader in customer experience management and contact centre business process outsourcing. Their company employs around 420,000 people working in over 265 dialects and languages, in 88 countries, operating across all business sectors and all continents on behalf of major international companies.br/ /ppOur client, with more than 4,700 employees in 10 sites in Spain (certified with Great Place to Work and Top Employer), is looking for a creative, data-driven campaign specialist.br/ /ppstrongPurpose of the role: /strong /ppIn this role, you will partner with an assigned portfolio of new clients in order to help them develop their first online advertising campaigns with the opportunity of having a significant impact on their business. It is a target-driven environment, where you will work towards individual targets as well as be part of a larger onboarding team.br/ /ppstrongResponsibilities /strong /pulliServe as a trusted consultant with customers to onboard and develop PPC Campaigns. /liliDetect and understand the customer’s needs and objectives. /liliBe responsible for increasing spend, upsell, and sustainability. /liliHandle a high volume of potential clients on a daily basis through phone calls. /li /ulh3Requirements /h3pstrongPreferred Skills and Experience: /strong /pulliBA/BS degree or equivalent (MA/MSc degree in Marketing, Digital Marketing or Communications can be a plus). /lili1-2 years minimum of work experience in sales and/or online advertising. /liliStrong desire to meet or exceed productivity, readiness, sustainability, and task points, compliance and customer satisfaction targets. /liliStrong verbal and written communication skills to pitch on the phone and compose compelling proposals. /liliGood time management skills and ability to organize their own day. /liliStrong analytical skills. /liliClient-focused, keen interest in customer interaction ownership of business goals. /liliA team player with ability to work in a fast-paced and constantly evolving environment. /liliSwedish C2 level. /liliHigh level of English. /li /ulh3Benefits /h3ulliFull-time position (39h per week, Monday to Friday). /liliSalary: 23,876€ gross/year + up to 3,408€ gross/year in bonus. /lilistrongThis is a Hybrid working model in Barcelona. /strong /liliPermanent Contract. /lilistrongRelocation support. /strong /lili2 to 4 weeks of intense introduction training on products and specific sales training. /liliEmployment with the world's largest provider of contact center services. /liliExcellent work environment, great colleagues, social arrangements and personal development. /liliOffice location surrounded by the sea (a World Trade Center /a, Barcelona, Spain). /li /ul #J-18808-Ljbffr