QC Microbiologist

• 17 juillet 2026 • 100% • Temporary • Neuchâtel • Log in to see the jobup.ch salary estimate Our partner, a major player in the pharmaceutical industry based in the canton of Neuchâtel, is looking for a Senior QC Microbiologist available immediately to strengthen its teams in a demanding and innovative GMP environment. Your responsibilities ## Within the Microbiology Quality Control laboratory, you will be responsible for performing and supervising microbiological analytical activities while contributing to the operational excellence of the laboratory. Main missions ### • Perform routine microbiological analyses on raw materials, intermediate products, and finished products. • Perform sterility tests, bioburden, endotoxins, and other associated microbiological analyses. • Ensure Environmental Monitoring and utility control activities. • Perform stability analyses and product release. • Participate in daily laboratory activities (preparation of reagents, sample management, inventories, orders of consumables, etc.). • Verify and review analytical data in accordance with GMP requirements. • Participate in laboratory investigations, deviations, CAPA, and Change Controls. • Identify, analyze, and resolve issues related to analytical methods and equipment. • Write and update procedures, work instructions, and quality documentation. • Ensure training and technical support for team members. • Contribute to continuous improvement, digitalization, and automation projects in the laboratory. • Participate in internal audits, regulatory inspections, and client audits. • Collaborate closely with Quality, Production, Validation, and Quality Assurance teams. Profile sought ## • Degree in Microbiology, Biotechnology, Biochemistry, or an equivalent scientific field. • Minimum 10 years of experience in Microbiological Quality Control within the pharmaceutical or biotechnological industry. • Solid experience in GMP/cGMP environments. • Excellent knowledge in: • Environmental Monitoring • Utility Monitoring • Sterility Testing • Bioburden • Endotoxin Testing (LAL) • Microbiological investigations • Significant experience in the management of deviations, CAPA, and Change Controls. • Knowledge of FDA and EMA regulations and USP/EP Pharmacopoeias. • Strong analytical capacity, problem-solving skills, and team spirit. • English minimum B2 What we are looking for ## We are primarily looking for an experienced, autonomous professional capable of quickly bringing technical expertise within a demanding pharmaceutical environment.