computer system validation csv

Als Computer System Validation Consultant werk je voor onze opdrachtgever aan het valideren van geautomatiseerde systemen binnen de Life Sciences-sector. Je bent verantwoordelijk voor het waarborgen van compliance, kwaliteit en data-integriteit van uiteenlopende systemen, variërend van laboratoriumapparatuur en productie-installaties tot complexe...

Evoke zoekt een Computer System Validation Consultant die aan de validation van geautomatiseerde systemen in Life Sciences werkt. Je waarborgt compliance, kwaliteit en data-integriteit van systemen variërend van laboratoriumapparatuur tot MES/LIMS/SCADA.Je stelt URS, validatieplannen, protocollen en risicoanalyses op en bewaakt GMP-, GAMP5- en FDA 21 CFR...

Johnson & Johnson is seeking a Sr. Manager - IM Computer System Validation Quality Lead to drive strategy and governance for CSV and AI usage in GxP-regulated activities.You will oversee lifecycle validation, risk-based approaches, and data integrity practices, while leading a global network of CSV leads and ensuring compliance across IM systems. The role...

Johnson & Johnson in Leiden seeks an experienced CSV Execution Lead to drive validation activities for automation, digital, and GMP-relevant systems across capital projects and day-to-day operations. You will plan, coordinate, and deliver validation work, coaching engineers and collaborating with multi-disciplinary teams to meet company standards.The role...

Senior CSV Specialist At Abbott Olst, we work every day on life-saving nutritional and pharmaceutical products. Within Manufacturing Automation, we are looking for a CSV Specialist who ensures reliable and compliant computerized systems. Location: Olst, The Netherlands. This is an onsite position that requires you to be onsite a minimum of 4 days a...

At Bristol Myers Squibb, our employees often ask, "Who are you working for?" - a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for...

Job DescriptionThe IM Computer System Validation (CSV) Quality Lead is responsible for assessing, implementing, and continuously improving the IM strategy for computer system validation and the use of embedded AI technology supporting GxP-regulated activities. This role ensures oversight that all IM systems are validated and maintained in a validated state...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across...

Bristol Myers Squibb Co. seeks a Senior Specialist for IT Quality and Computerized Systems Validation in Leiden.You will provide hands‑on CSV/IT compliance support for the Cell Therapy Facility, acting as SME on CSV matters and aiding audit readiness and regulatory responses. Responsibilities include developing validation documentation, reviewing...

At Bristol Myers Squibb, our employees often ask, \"Who are you working for?\"-a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for...

Bachem Holding AG is seeking a Quality Engineering Manager CSV to lead qualification and validation of computerized systems for our new Sisslerfeld site. You will drive CSV activities from design through operational phases, ensuring GMP compliance and inspection readiness.Ideal candidates have 3+ years in pharma CSV within CAPEX projects, strong regulatory...

Contract and Permanent Roles | Start: Potentially Q3-Q4 2025 (Multiple locations in the Netherlands) About KPC International KPC International is a consulting and engineering firm established in 2001. We support global pharmaceutical and biopharmaceutical clients through all phases of Plant Facility Start-Up, from strategic planning and execution through to...

Job Role: Automation Specialist - QC LaboratoriesAbout the Role: We are seeking an experienced Automation Specialist to support QC laboratories in a pharmaceutical environment. This role focuses on laboratory automation, computerized systems, data integrity and GMP compliance. You will act as a Subject Matter Expert (SME) for laboratory systems, supporting...

Quality Engineering (QE) Manager CSV - Sisslerfeld (a) 100% Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology...

Abbott Laboratories in Olst, The Netherlands, is seeking a Senior CSV Specialist to ensure reliable validated computerized systems. This onsite role requires collaboration with QA, Operations, IT and Engineering to maintain GMP compliance and data integrity.You will lead validation projects, develop CSV standards, translate regulations such as NIS2 and GMP...