data engineer Jobs in Europe

Devops / Cloud Engineer (Azure) - Híbrido (Manresa, Cataluña ) - €45.000 - €50.000 Al Año

Se busca un Ingeniero DevOps/Cloud con experiencia en Azure, Kubernetes y arquitecturas cloud para diseñar, implementar y mantener soluciones, participando en migraciones y transformaciones de infraestructura en Manresa.

Purchasing Engineer Aw

Lead technical purchasing for new heat pump components, managing time-to-market processes, supplier relations, and cost initiatives. Requires engineering degree and 4 years of purchasing experience.

Ai Data Enablement Engineer

Se busca un Ingeniero de Datos para consolidar datos de negocio, integrarlos en un Datawarehouse y dar soporte a herramientas de explotación de datos, con experiencia en SQL y Python.

Mechanical Engineer

Mechanical Engineer needed for a growing tech company in Terrassa. Responsibilities include product development, 3D modeling, supplier management, prototyping, and industrialization support. Requires a Bachelor's degree in Mechanical Engineering, 2+ years of experience, and CAD/PLM proficiency.

Ai-Driven Operational Excellence Lead

SmartRecruiters, Inc. is seeking an Operational Excellence Engineer to support the General Manager in strategic planning, prioritization, and alignment across the plant, driving safety, quality, delivery, cost, productivity, and people development. You will prepare executive reports, lead AI-driven KPI analysis, coordinate cross-functional initiatives, manage budgets, and promote governance and accountability within a Business Excellence framework. This full-time, on-site role is based in Spain.

Product Engineer - €38.000 - €42.000 A Year

Automotive Product Engineer needed for mechanical component development, focusing on technical feasibility, industrialization, and cross-functional coordination. Requires engineering degree and 2-3 years experience.

Staff Software Engineer, Site Reliability Engineering, Google Cloud - €156.000 A Year

Seeking a Staff Software Engineer for Site Reliability Engineering at Google Cloud in Munich or Zurich. Requires 8 years of software development experience and expertise in distributed systems.

Lead Central Monitor - €63.600 - €118.000 A Year

Salary Range: €63,600.00 - €118,000.00 Job Description Summary Role Type: Hybrid Working, #LI-Hybrid Primary Location: Barcelona, Spain Other Locations: London, United Kingdom; Dublin, Ireland Relocation Support: This role is based in Barcelona, Spain. Novartis is unable to offer relocation support: please only apply if accessible. What if your leadership could transform how clinical trial risks are identified, understood, and managed across a global development portfolio? As Lead Central Monitor, you will lead and develop a team of Central Monitors while shaping monitoring strategies that protect patient safety, trial quality, and data integrity. Working across clinical, data, and risk-surveillance teams, you will turn complex information into actionable insights, strengthen risk-based monitoring practices, and help advance the Central Monitoring capability at Novartis. Key Responsibilities Lead and develop a team of Central Monitors, building capability, engagement, and consistently high performance. Shape central and site monitoring strategies tailored to program, study, and Development Unit risks. Oversee trial-data surveillance, risk reviews, signal detection, and insight generation using Central Monitoring technology. Translate complex risk signals into actionable insights that enable Clinical Trial Teams to investigate and resolve issues. Partner with clinical, data, and risk-surveillance teams to implement effective monitoring and risk-mitigation approaches. Guide protocol development, risk assessment, and the design of study-specific Key Risk Indicators and thresholds. Ensure monitoring activities support clinical data integrity, regulatory compliance, audit readiness, and timely issue resolution. Drive continuous improvement through analytics, technology, innovation, lessons learned, and Risk-Based Quality Management. Essential Requirements University degree in Life Sciences, Business, Operations, or a related discipline. At least seven years of recent pharmaceutical or contract research organisation experience, including experience in clinical research. At least five years of experience in central or site monitoring, clinical data analytics, data management, or a related discipline. At least three years of recent people-management or team-leadership experience, with proven ability to develop high-performing teams. Strong understanding of clinical trial development, study execution, protocols, study risks, and clinical trial risk-management processes. Experience with centralised monitoring, Key Risk Indicators, Quality Tolerance Limits, and Risk-Based Quality Management approaches. Strong knowledge of Good Clinical Practice, International Council for Harmonisation standards, and relevant health-authority requirements. Strong analytical, digital, communication, and problem-solving skills, with the ability to interpret complex data and influence stakeholders in a global matrix environment. Desirable Requirements Advanced university degree. Extensive knowledge of a relevant therapeutic area. Experience using artificial intelligence, analytics, or other digital approaches to support transformation. Manager-of-managers experience and a track record of developing diverse, high-performing teams. Benefits & Rewards Expected Annual Base Salary Range for role: €63,600 to €118,000. The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. The rewards of being part of our team go far beyond base pay and incentives. Read our brochure to learn more about our global total rewards offering: Read our handbook (PDF 30 MB). Competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. Flexible and hybrid working options, where possible. Minimum 14 weeks paid parental leave. Commitment to Diversity & Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Why Novartis Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? Skills Desired Budget Management, Clinical Research, Clinical Study Reports, Clinical Trials, Collaboration, Data Analysis, Health Sciences, People Management, Regulatory Compliance. Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. #J-18808-Ljbffr

Senior Soc Analyst

Syntegon Telstar S.R.U is a company belonging to the Syntegon Group, which operates worldwide with 7,300 colleagues at 49 locations in over 20 countries.Is a company belonging to the Syntegon Group, which operates worldwide. As a brand specialising in the development of GMP consulting, engineering, construction and integrated process equipment projects, we serve companies linked to the life sciences market (pharmaceutical and biotechnology, healthcare, cosmetics, veterinary and food industries), as well as hospitals, laboratories and research centres. We also offer solutions using vacuum and high vacuum technologies for traditional and high-tech industries in the energy and aerospace sectors, as well as scientific experimentation. Qué quedes esperar: We are looking for a Senior SOC Analyst to join our team at our offices in Terrassa (Barcelona) . In this Tier 3 role, you’ll lead the detection, triage, investigation, and response to complex security threats across the organization while serving as a key technical escalation point for critical incidents. You’ll also mentor junior analysts, improve SOC processes, strengthen detection and response capabilities, and help drive the continued maturity of our security operations. The ideal candidate brings deep knowledge of the threat landscape, strong incident response expertise, and a passion for building an effective, collaborative, and resilient SOC. Key Responsibilities Lead the triage, investigation, and escalation of complex or high-severity security alerts across endpoint, network, identity, cloud, and application domains. Drive end-to-end incident response for significant security events, coordinating across IT, Cloud, Identity, and business stakeholders and producing thorough incident reports with root cause analysis and remediation recommendations. Conduct proactive threat hunts based on intelligence and known adversary TTPs, identifying detection gaps and working with the SOC Engineer to translate findings into improved detection content. Leverage SOAR platforms to execute and refine automated response workflows, identifying repetitive tasks and escalating automation opportunities to the SOC Engineer. Develop and maintain IR playbooks, runbooks, and SOPs, contributing to process improvements based on lessons learned and operational gaps. Act as a coach and escalation point for Tier 1–2 analysts, contributing to training, knowledge sharing, and a culture of continuous learning. Ensure incident handling aligns with relevant compliance requirements and maintain accurate, audit-ready case records and evidence documentation throughout the investigation lifecycle. Qué aportarás: Required Qualifications: 4–6+ years in cybersecurity with 3+ years in a SOC analyst or incident response role. Deep understanding of the incident response lifecycle with proven experience handling complex, multi-domain security incidents. Strong knowledge of attacker TTPs, threat actor behaviour, and the MITRE ATT&CK framework. Solid analytical skills across endpoint, network, identity, and cloud attack vectors. Familiarity with SOAR platforms and experience working within automated triage and response workflows. Understanding of threat intelligence concepts and how to apply them to detection and investigation. Strong written and verbal communication skills with the ability to produce clear incident reports for both technical and non-technical audiences. Preferred Qualifications: Certifications: GIAC (GCIH, GCFA, GCFE, GCIA, GMON), CISSP, or equivalent industry certifications. Experience with threat hunting methodologies and proactive adversary detection techniques. Exposure to scripting or automation concepts (e.G., Python, PowerShell) to support workflow improvements. Experience working within or alongside MSSP/MDR environments. Familiarity with forensic analysis, malware triage, or reverse engineering. Exposure to data privacy, eDiscovery, and chain-of-custody requirements during investigations. Información adicional Availability to travel (approximately 10–20%) when required (HQ in Germany). Por Syntegon y sus subsidiarias, la diversidad es una preocupación clave. Exclusivamente promocionamos un ambiente donde todos los empleados, independientemente de su género, edad, origen, religión, orientación sexual, identidad de género o necesidades especiales, sean tratados de manera equitativa. Si esta oferta de trabajo utiliza únicamente la forma masculina, es por razones de legibilidad y se refiere a individuos de todos los géneros. #J-18808-Ljbffr

Gerocultor/A Turno Noche - €9,7 Por Hora

Gerocultor position providing daily living assistance, support with autonomy habits, postural changes, meal support, sociocultural activities, personal hygiene, and data registration for elderly individuals.

Product Engineer

Sector : Automotive | Product Development | Mechanical Components At K-LAGAN , we are looking for a Product Engineer to join a technical project within the automotive sector, focused on mechanical product development, technical feasibility and industrialization. This role is ideal for professionals with hands‑on experience in product engineering, mechanical product development and cross‑functional coordination with design, quality, manufacturing, purchasing, suppliers and customer engineering teams . Responsibilities Ensure the technical feasibility of the product during offer and development phases. Apply standardized solutions and lessons learnt throughout the product development process. Participate in design reviews and support technical decision-making. Ensure prototype development and delivery according to customer and project milestones. Participate in product and process FMEA activities. Analyze technical test results and collaborate on the definition of technical countermeasures. Work closely with manufacturing teams during product industrialization. Manage product modifications during the development phase. Support cost, quality and product performance improvement through technical solutions and benchmark analysis. Cooperate with purchasing teams and suppliers to optimize components in terms of cost, quality and manufacturability. Ensure CAD 3D and 2D design development. Act as a technical interface with customer engineering teams. Requirements Degree in Engineering or equivalent experience. Minimum 2-3 years of experience in a similar role. Experience with CAD 3D/2D design and technical documentation. Knowledge of FMEA, product testing, prototypes and industrialization phases. Experience working with manufacturing, quality, purchasing or supplier teams. Fluent Spanish, English and German, spoken and written. Previous experience in the automotive sector will be highly valued. Experience with plastic parts, exterior components, rear-view systems or vision systems will be a plus. Why K-LAGAN? We are an international strategic technology services company. We work on high-impact projects, offering our team the opportunity to grow personally and professionally within a dynamic, inclusive and people-centered culture. Benefits Permanent contract and stable project. Team buildings, tech coffees and internal events, including Solidarity Day, Christmas dinner and summer events. Continuous follow-up and feedback. Career development and training department. Birthday day off. Additional social benefits: childcare support, mileage allowance, language courses and more. The expected salary range for this position is between €38,000 and €42,000 gross per year . However, the final offer will be adjusted according to the candidate’s experience, technical skills, soft skills and the value they can bring to the project. #J-18808-Ljbffr

Demand Planner Iberica (F/M/D) - €35.000 - €40.000 A Year

Working at Freudenberg: We will wow your world! Responsibilities: - Own and lead the demand forecasting process for your category, ensuring high forecast accuracy and optimal product availability across short, mid, and long-term horizons (volume and value)- Act as a key partner for Sales and Marketing, translating market trends, promotions, launches, and delistings into reliable demand plans- Maintain, review, and continuously improve forecasting models, planning master data, and replenishment strategies in SAP / IBP- Play a key role in the S&OP process, preparing data, supporting consensus meetings, and providing clear insights on availability, promotions, and lifecycle activities (phase-in/phase-out)- Monitor forecast accuracy, stock levels, and service levels (SFD, CSL, ICSL, SSL), analyzing deviations and driving continuous improvement actions- Manage ordering from production sites, suppliers, and co-packers, ensuring timely deliveries aligned with the sales and production plans- Coordinate co-packing activities, balancing product availability, cost efficiency, production scheduling, and raw material supply- Handle supply chain topics including quality issues, SLOB management, and process improvements to increase operational efficiency Qualifications: Relevant higher education or minimum 5 years of professional experience in Supply Chain, Demand Planning or related functionsSolid experience in demand forecasting, preferably in FMCGAdvanced Excel skills and strong working knowledge of SAP / IBP / BI toolsVery good command of English (minimum B2), enabling effective communication in an international environmentStrong analytical background (statistics, data analysis, business interpretation)Excellent communication skills, with the ability to influence stakeholders and challenge assumptionsProactive, self driven mindset with ownership for results Min 35.000€- Max 40.000€ annual amount

Senior Composite Design Engineer - F1

At BOLD, we design and build the next generation of high-performance battery systems for the world’s most demanding industries — from Formula 1 and hypercars to aerospace, marine and defense. Our mission: to deliver energy systems where every millisecond and every degree matter. As a Senior Composite Design Engineer - F1, you will play a key role in the design and development of composites laminates, and structures. You should possess an understanding of the materials and processes utilized in high-end composite structures applications (Prepreg, cores, tooling, and trimming methodologies). What You Will Do Analysis and verification of initial specifications. Statements of works – Drawing and layup table specification Experienced in design and developing of composites laminates and structures. Full understanding of material and processes used in high end applications composites structures (Prepreg, cores, mouldings and trimming methodologies) Experience in the design and manufacturing process of composites tooling, patterns and CFRP moulds for autoclave and OoA processes Experience designing of composites components and tooling using CATIA V5 or Siemens NX. Good work practice of surfaces and solids. Broad understanding of CATIA/NX functions and the structuring of Generator files, publications and save management structure for large master product files Excellent understanding or parametric modelling and stable tree structures required to support agile geometry development Experience in drafting of drawings using CATIA V5 (V6)/Siemens NX for composites component, tooling, jigs, and fixtures to support manufacturing requirements. Understanding of the applications of GD&T and process limitations of composites materials when tolerancing and defining geometries Excellent time management and leadership skills, able to support Jr designers with technical queries in both materials and CATIA/NX structures for parametric modelling Able to work to a project plan and manage technical requirements vs workload to a schedule, maintain active communication in an agile environment of adherence to project plans and set targets. Leveraging on cloud base collaborative platforms such as MS Office suite and Cloud project management tools Maintain an up-to‑date technical awareness of the business requirements Work closely with the technical leads and Project management office to coordinate and effectively plan and program the designs to ensure the assembly team have enough time to meet key dates and deadlines Minimum Requirements What You Bring +5 years of experience working as a Composite Design Engineer EV/Motorsport industry experience Mechanical Engineering Degree or equivalent R&D design experience Excellent knowledge and experience of Catia v5/3DX and/or Siemens NX Structural Design experience In‑depth knowledge of composite manufacturing processes, especially for prepreg components, including tooling, inserts, cores, and all associated processes Proficient English Desirable Skills FEA and/or CFD experience Vast knowledge of materials used in motorsport and aerospace applications (metallic alloys/technical polymers/composites) Why Join BOLD High‑growth, multicultural environment: Be part of a fast‑scaling company driving innovation in advanced electrification. Competitive Compensations Life Insurance Private health insurance - Reduced cost for employees and family. Subsidised canteen Flexible work schedule and up to 5 remote days/month. Monthly Town Hall About BOLD At Bold, we’re a diverse, international team with backgrounds in automotive, motorsport, aerospace, defense and aviation. We combine creativity and engineering rigour to deliver high‑performance, safe and sustainable energy systems for the world’s most demanding applications. We Operate Through Two Divisions BOLD Applied Engineering (BAE )– Provides top‑tier professional engineering services, primarily to elite motorsport teams (especially Formula 1), in areas such as composite design, mechanical engineering, aerodynamics and systems integration. This expertise is transferred directly to complex defence sector programmes. BOLD Technology (BT) – Designs, develops and manufactures high‑voltage battery systems and electric propulsion system components for defence applications, tactical vehicles, military platforms, aviation and advanced mobility. BOLD is an international benchmark in defence electrification, supplying systems to United States Army programmes and collaborating with leading defence primes in the US and Europe. Inclusion & Diversity BOLD is an equal opportunity employer. We foster a culture where ideas thrive based on merit and competence, regardless of age, disability, race, religion, gender, sexual orientation, or family circumstances. Privacy Policy BOLD respects your privacy and is committed to protecting the personal information you share with us, please refer to Bold’s Privacy Policy for more details. #J-18808-Ljbffr

Senior Expert Cloud Data & Ai Architect - Healthcare

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you've got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. ¿Es usted el solicitante adecuado para esta oportunidad? Descúbralo leyendo el resumen del puesto a continuación. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. Your Role: As a Senior Cloud Data & AI Architect within the Healthcare Architecture Team, you will design and govern cloud-native architectures that enable scalable data, analytics, AI/GenAI, and agentic AI solutions across the healthcare portfolio. You will partner with Data & AI, Security, Platform, and cross-functional Healthcare teams to define standards, drive reference architectures, and enable governed solutions across AWS, Snowflake, Palantir Foundry, and related technologies. This role combines deep cloud engineering with data, AI/ML, and agentic workflow architecture to accelerate value delivery while ensuring compliance, security, reliability, and responsible AI. Design end-to-end cloud architectures on AWS and connected data platforms, including Snowflake and Palantir Foundry. Define and govern reusable patterns for data ingestion, storage, processing, analytics, and AI/ML workflows. Lead the architecture of AI/ML and GenAI capabilities, including MLOps, model monitoring, and risk controls. Embed security, privacy, data governance, resilience, and cost management into solution designs from the start. Evaluate platform and integration choices to improve performance, scalability, and total cost of ownership. Promote architecture standards and best practices; create reference architectures, design documents, roadmaps, and runbooks; and mentor engineers and architects on automation and infrastructure as code. Collaborate with cross-functional Healthcare teams to translate business priorities into scalable, secure, and compliant data and AI solutions. Define reusable architecture patterns for agentic AI solutions, including agent orchestration, retrieval-augmented generation, tool integration, human-in-the-loop controls, evaluation, observability, and governance. Who You Are – Minimum Qualifications Bachelor's degree in computer science, information technology, engineering, or a related field. 6+ years of experience in cloud architecture, cloud engineering, or a closely related technical role. Hands-on expertise designing solutions on AWS, including identity and access management, storage, compute, serverless, data, and security services. Experience with at least one enterprise data platform, such as Snowflake or Palantir Foundry. Experience designing and delivering AI/ML or GenAI infrastructure, including data pipelines, deployment, monitoring, and governance. Knowledge of data governance, data quality, privacy, security, and regulated-data considerations, including PII/PHI and GxP-relevant contexts. Proficiency in Python and SQL, plus infrastructure-as-code tooling such as Terraform or CloudFormation. Experience designing or delivering GenAI and agentic AI solutions, including large language model application architecture, retrieval-augmented generation, agent orchestration, tool integration, evaluation, monitoring, and responsible-AI controls. Preferred Qualifications Master's or doctoral degree in a related discipline. AWS certifications, such as Solutions Architect, Data Analytics, or Machine Learning Specialty. Experience with clinical, research, manufacturing, regulatory, commercial, or supply-chain data in a healthcare or life-sciences environment. Experience leading architecture governance forums and developing enterprise standards, data lineage, metadata, or integration practices. Experience delivering scalable, multi-service data and AI platforms in regulated environments. Experience applying agentic workflows to regulated healthcare or life-sciences use cases, with security, privacy, auditability, and human-oversight controls. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! xqysrnh Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Auxiliar Administratiu/Iva Amb Experiència Àmbit Sanitari - €11.938,2 Per Any - Tiempo Parcial

Administrative assistant with experience in the healthcare sector needed for a center in Mollet del Vallès. Responsibilities include patient reception, appointment scheduling, data entry, and support.

Regional Head, Pharmacovigilance Quality

Salary Range: €69,100.00 - €128,300.00 Job Description Summary #LI-Hybrid Location: Barcelona, Spain This role is based in Barcelona, Spain. Novartis is unable to offer relocation support for this role. Please only apply if this location is accessible for you. The Regional PV QA Head provides end to end quality assurance vigilance expertise and support to global and local operational Pharmacovigilance (PV) and Device Vigilance activities within Novartis with a focus on the country organizations, as well as quality expertise in regional and local vigilance regulation, in order to ensure compliance with applicable regulatory requirements and Novartis procedures. Job Description Drive independently the regional and country quality oversight for implementation and maintenance of Novartis vigilance Quality Systems performed by the local teams, namely Quality Issue, proactive risk assessment and action management systems. Ensure, together with PS and PV in Countries and Regions team, that regional and country quality performance of the Novartis Vigilance System tasks and responsibilities is performed as required under global, regional and country PV regulations, to monitor that safety of the Novartis authorized products are met, and changes to their risk-benefit balance are identified. Support the regional and country Global Research and Development Quality management cycle through development, execution and accountability for deliverables of the global vigilance Quality Plan (QP). Coordinate execution of the QP with relevance to applicable regional and country patient safety activities and report the status to applicable Global PV QA team. Monitor indicators that relate to the performance, compliance and quality of regional and country vigilance systems, in line with indicators defined by Global PV QA team. Act as a quality champion by communicating risks to PS and PV and providing recommendations on potential mitigations. Promptly communicate regional and country compliance issues to Global PS&PV, PV QA management and QPPV. Proactively propose potential quality improvement measures and develop strategies aimed at simplifying processes and improving quality of outputs while ensuring compliance with regulatory requirements; share best practice within and across regions. Lead regional initiatives focused on quality improvement and compliance, provide ongoing project support and governance, as assigned. Provide expertise and support Global PV QA team in the execution of vigilance Quality Risk Assessments (QRA) to identify and mitigate regional and country PV risks. Support maintenance of the Novartis global Pharmacovigilance System Master File (PSMF), where applicable. Ensure a constant state of regional and country vigilance inspection readiness. In line with Global PV QA and PS&PV teams, prepare for, facilitate, provide expertise and lead logistics for Health Authority (HA) vigilance inspections, assess results of pre-inspection activities and HA inspection findings in terms of associated risks and communicate to management. Perform Quality check of vigilance inspection deliverables. Align with PS and PV team and review the inspection corrective and preventive (CAPA) plan, to ensure quality, consistency and appropriateness of commitments. Act as the functional QA approver of inspection CAPA plans from the PV inspections in country organizations in the QMS. Monitor the status of implementation of the CAPAs and approve the related evidence in the QMS, to ensure they are completed, appropriately documented and sustainable. Expertly guide the development of robust and sustainable CAPAs to address PV audit findings related to country organizations and act as functional QA approver of the CAPA plan in the QMS. Monitor the status of implementation of CAPAs to ensure they are completed, appropriately documented and sustainable and approve applicable related evidence in the QMS. Provide expertise and support country PS and PV and other business partners with identification and compliance of-Quality Issue investigations, act as functional QA in the QMS and ensure timely escalation of applicable Quality Issues to management; provide assistance in the remediation of PV system issues; ensure follow-up and monitoring of completeness of CAPAs in alignment with PV QA team. Oversee definition of PV self-assessment plans from Regional PS & PV team to regional and country pharmacovigilance processes as well as their execution. Review vigilance self-assessment reports and approve related action plans in the QMS. Identify regional and local training needs (for example via Quality Issues) and deliver knowledge sharing sessions that meet the needs of business and QA partners and improve overall quality and compliance of the Vigilance system. Provide guidance and recommendations on Merger & Acquisition as well as divestment relevant activities for integration or disintegration of the vigilance system, where applicable. Lead and/or support due diligence (DD) activities for potential product and/or company acquisitions, when applicable. Minimum Requirements Degree in Life Sciences or related scientific discipline. Higher degree desirable. Excellent written and verbal English communication skills; fluency in a second language a plus. Quality/ PV/ clinical/ regulatory affairs/ pharmaceutical industry/ health authority experience; GCP/PV/GMP auditing or inspection experience and Health Authority interactions a plus. Experience in PV in a country organization and global quality support to stakeholders in country organizations a plus. Ability to travel up to 20%. Ability to independently manage and objectively evaluate complex compliance issues with minimal supervision; Excellent problemsolving, decision making and prioritization skills. Quality mindset and excellent quality and compliance leadership and facilitation skills. Extensive knowledge of PV regulations, guidelines and policies; Awareness of GCP and Part 11 requirements. Ability to lead teams and operate successfully in various team capacities and diverse cultural environments. Ability to deputize for the Global Head PV QA Regions and Countries as needed. Benefits & Rewards At Novartis, we’re committed to reimagining medicine together - and rewarding the people that make it happen! Expected Annual Base Salary Range for role: 69,100.00 -128,300.00 EUR The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. Read our brochure to learn more about our global total rewards offering: Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. Skills Desired Business Acumen, Business Partnerships, Change Management, Communication, Continuous Improvement, Data Integrity, Digital Fluency, Ensure Compliance, GMP Operations, Good Laboratory Practices (GLPs), Good Manufacturing Practices (GMP), Leadership, Managing Ambiguity, Organizational Savvy, Problem Solving, Process Improvements, Quality Assurance (QA), Quality Compliance, Quality Management (QMS), Regulatory Compliance, Risk Management, Stakeholder Management, Storytelling, Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. #J-18808-Ljbffr

Postdoc Position - €31.211 A Year

As a flagship research center in nanoscience and nanotechnology, our mission is to open and explore new frontiers of knowledge at the nanoscale and bring value to society in the form of new understanding, capabilities, and innovation, while inspiring and providing broad training to the next generations of researchers. Our values are Commitment, Collaboration and Transformation. Our research lines focus on the newly discovered physical and chemical properties that arise from the behaviour of matter at the nanoscale. ICN2 has been awarded the Severo Ochoa Center of Excellence distinction for three consecutive periods , and ). ICN2 comprises 20 Research Groups, 7 Technical Development and Support Units and Facilities, and 2 Research Platforms, covering different areas of nanoscience and nanotechnology. Job Title: Postdoctoral ResearcherDepartment: Thermal Properties of Nanoscale MaterialsDescription of Group/Project:The Thermal Properties of Nanoscale Materials (GTNaM) group at ICN2/UAB investigates nanoscale thermal phenomena, molecular glasses, and functional materials. This position is funded by GLASSPIKE, an ERC Advanced Grant developing vapor-deposited molecular glasses with programmable polarization for analog memory and spike-based computing. The researcher will work in a multidisciplinary environment combining thin-film growth, AFM/KPFM, electrical characterization, nanostructuration, and nanocalorimetry. Main Tasks and responsibilities:Grow and optimize vapor-deposited molecular-glass thin films. Characterize spontaneous molecular orientation, polarization, and surface potential. Develop quantitative KPFM and FM-KPFM methods for highly polar molecular films. Investigate voltage-driven molecular polarization and depolarization. Generate and characterize programmable analog polarization states. Correlate KPFM with thermally stimulated depolarization and pseudopyroelectric measurements. Study interfacial imprinting, relaxation, and stability of programmed states. Investigate devitrification and local transformations; analyze results and prepare publications. Requirements:Education : PhD in Physics, Materials Science, Nanoscience, Physical Chemistry, Electrical Engineering, or a closely related field. Knowledge : Surface/contact potential, dielectric and polarization measurements, thin-film physics and data analysis.Essential research profile : Applications will be considered only from candidates whose peer-reviewed publications demonstrate direct research experience in all three core areas:Kelvin Probe Force Microscopy (KPFM), preferably quantitative KPFM or FM-KPFM; Ferroelectric, pyroelectric, electret, or related polarization phenomena; Molecularorganic materials or organic thin films. Applications that do not document this experience will not be considered. Professional Experience: Hands-on AFM/KPFM and electrical characterization of polar materials. Experience in thin-film growth, current measurements, or experimental instrumentation is desirable. Personal Competences: Scientific independence, rigorous experimental practice, teamwork, and strong written and oral communication in English. Summary of conditions:Full-time work (37,5h/week) Contract Length: Temporary; 36 months (M1-M36), linked to the GLASSPIKE project Location: Bellaterra (Barcelona) Salary will depend on qualifications and demonstrated experience. Support for relocation issues. Life Insurance. Estimated Incorporation date: 01/02/2027 “Funded by the European Union and European Research Council – Grant No – GLASSPIKE” Equal opportunities:At ICN2, we foster an inclusive and safe work environment, free from any form of discrimination—whether based on gender, sexual orientation, gender identity, age, origin, culture, religion, disability, or any other personal or social condition. We are committed to ensuring equal treatment and opportunities in all our processes, especially in recruitment, which is based solely on talent, experience, and ability. We implement proactive policies for inclusion and harassment prevention that reinforce our commitment to respect and fairness. If you share these values and are looking to grow in an open and diverse environment, ICN2 is ready to welcome you. #J-18808-Ljbffr

Staff Software Engineer, Site Reliability Engineering, Google Cloud

Seeking a Staff Software Engineer for Site Reliability Engineering at Google Cloud in Munich or Zurich. Requires 8 years of software development experience and expertise in distributed systems.

German-Speaking Corporate Sales Engineer (Remote) - Remote

Sales Engineer to support German Corporate Team, responsible for technical demonstrations, product configuration, and client requirement gathering for cybersecurity solutions.

(Senior) Software Engineer (All Genders)

Merck Group in Spain seeks an Analytics Architect within the Enabling Functions Data Office to design and deliver high-impact data and AI solutions that power smarter ways of working across the organization. You will join a collaborative, internationally distributed team delivering data products at scale in a Product-Oriented Delivery model. You will work with Snowflake, AWS, Palantir Foundry and end-to-end data pipelines, focusing on governance, security, and regulatory compliance while #J-18808-Ljbffr