QC Microbiologist

• 17 juillet 2026
• 100%
• Temporary
• Neuchâtel
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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.