gmp documents

ppCLEEVEN is a European consulting company founded around two core convictions: /p ulliEuropean engineering excellence should be a driver of global competitiveness /liliOur human mission is to support our consultants in their personal and professional development /li /ul h3Project Context: /h3 pAs part of a Document Management transformation program within a...

Your responsibilitiesMaintain compliance with GMP requirements and applicable quality regulations across manufacturing processes and finished products.Review, develop and update SOPs, work instructions and quality documentation, ensuring these are followed consistently in daily operations.Assess production and batch documentation for accuracy and compliance,...

h3Your responsibilities /h3ulliMaintain compliance with GMP requirements and applicable quality regulations across manufacturing processes and finished products. /liliReview, develop and update SOPs, work instructions and quality documentation, ensuring these are followed consistently in daily operations. /liliAssess production and batch documentation for...

Your responsibilitiesMaintain compliance with GMP requirements and applicable quality regulations across manufacturing processes and finished products.Review, develop and update SOPs, work instructions and quality documentation, ensuring these are followed consistently in daily operations.Assess production and batch documentation for accuracy and compliance,...

pBristol Myers Squibb in Switzerland is seeking a Senior Specialist Process Excellence Compliance to lead Quality Events management and support inspection readiness and regulatory audits. You will own quality events (CAPAs, change controls, complaints, deviations), maintain GMP documents, and ensure timely approvals through the document system. /ppThe role...

SKAN in Allschwil (Basel-Landschaft) is recruiting for its production team. You will manufacture biological indicators, document every step, and ensure GMP-compliant processes in a structured environment.Ideal candidates have 3+ years in GMP manufacturing, strong attention to detail, and German/English language skills. Prior microbiological experience is a...

pITech Consult AG in Switzerland is seeking a Chemical Laboratory Technician to join our QC team. You will perform inspection and testing of reagents and materials, document results, and ensure GMP-compliant records and reports while coordinating with QA, Purchasing and Production. /ppThe ideal candidate holds EFZ in chemical lab or a B.Sc. in Chemistry, has...

pEurofins Scientific is a leading international life sciences company focused on delivering analytical testing services across industries. The role involves leading projects for implementing new analytical methods and equipment in the microbiological lab, coordinating with QA and suppliers, and ensuring GMP compliance, timelines, and quality deliverables....

pWe are currently seeking a detail-orientedb GMP Documentation Specialist (m/w/d) /b to join our client’s Manufacturing Operations team in a dynamic, fast-paced biopharmaceutical environment. /p pThe GMP Documentation Specialist supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation...

pResourcing Life Science Ltd. is seeking a seasoned Quality Assurance professional to oversee GMP compliance, review and update quality documents, and drive CAPA actions across manufacturing and quality operations. /ppYou will assess batch documentation, investigate quality incidents, and coordinate corrective actions in collaboration with cross-functional...

Incyte in Switzerland seeks a Compliance Specialist to manage deviation, CAPA and risk management. You will support cGMP and site quality goals in manufacturing, lead continuous improvement projects and review manufacturing documents to ensure compliance.The role requires 3–5 years in biotech quality with strong analytical skills, and fluency in English...

pLonza Visp site in Switzerland seeks a Senior QA Specialist / Customer Audit Manager with a strong scientific background and GMP experience to lead customer audits and internal/regulatory inspections. You will coordinate audit planning, document findings, and present Lonza's QA systems to customers. /ppFluent English and German, plus a degree in...

Lonza Visp site in Switzerland seeks a Senior QA Specialist / Customer Audit Manager with a strong scientific background and GMP experience to lead customer audits and internal/regulatory inspections. You will coordinate audit planning, document findings, and present Lonza's QA systems to customers.Fluent English and German, plus a degree in...

Resourcing Life Science Ltd. is seeking a seasoned Quality Assurance professional to oversee GMP compliance, review and update quality documents, and drive CAPA actions across manufacturing and quality operations.You will assess batch documentation, investigate quality incidents, and coordinate corrective actions in collaboration with cross-functional teams....

Lonza Visp site in Switzerland seeks a Senior QA Specialist / Customer Audit Manager with a strong scientific background and GMP experience to lead customer audits and internal/regulatory inspections. You will coordinate audit planning, document findings, and present Lonza's QA systems to customers.Fluent English and German, plus a degree in...

We are currently seeking a detail-oriented GMP Documentation Specialist (m/w/d) to join our client’s Manufacturing Operations team in a dynamic, fast-paced biopharmaceutical environment. The GMP Documentation Specialist supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation supports...

Resourcing Life Science Ltd. is seeking a seasoned Quality Assurance professional to oversee GMP compliance, review and update quality documents, and drive CAPA actions across manufacturing and quality operations.You will assess batch documentation, investigate quality incidents, and coordinate corrective actions in collaboration with cross-functional teams....

Bachem Holding AG in Bubendorf is seeking a dedicated Manager QA Projects (a), 100% to strengthen the Quality Assurance team. You will represent QA in product-related projects at the Bubendorf site and ensure cGMP compliance across Production, QC and Project Management.Responsibilities include defining control and lifecycle strategies from development...

Try&Hire is seeking a scientifically minded professional to develop oral solid dosage formulations and lead manufacturing process development in Basel, Switzerland. The role covers from early-stage to GMP-compliant production, with onsite work and potential permanent placement after interim period.You will plan experiments with cross-functional teams,...

Incyte is seeking Production Technicians to support GMP-driven manufacturing operations. You will control production tools, execute tasks per schedule, participate in area maintenance, and document deviations in quality systems.Responsibilities include batch release review, equipment qualification, 5S-driven improvements, and training of team members while...