Description

Microbiology Specialist (6-Month Contract)
Project Lead-Release/stability Testing-Environmental&Utility Monitoring
Are you an experienced QC Microbiology professional looking for your next challenge in a highly regulated pharmaceutical environment?
Our client, an internationally operating pharmaceutical company in the Neuchâtel area, is looking for a Specialist – Quality Control Microbiology Laboratory to support its Quality Control team. This is an excellent opportunity to contribute to microbiological testing, laboratory excellence, and continuous improvement within a GMP environment.
Your Responsibilities
Perform microbiological testing of raw materials, intermediates, finished products, environmental and utility monitoring samples
Execute release and stability testing using compendial and validated microbiological methods
Review and verify laboratory data while ensuring full GMP compliance
Support laboratory operations including reagent preparation, inventory management, sample handling, and equipment maintenance
Investigate laboratory deviations, support change controls and continuous improvement initiatives
Prepare and update laboratory procedures, work instructions, and technical documentation
Train colleagues and contribute to laboratory projects, process optimization, and digitalization initiatives
Collaborate with cross-functional teams and support internal and regulatory inspections when required
Your Profile
Laboratory Technician qualification (or equivalent) with at least 12 years of practical laboratory experience, or a Bachelor's/Master's degree in a scientific discipline with at least 1-2 years relevant QC Microbiology experience
Extensive hands-on experience in QC Microbiology within the pharmaceutical or biotechnology industry
Strong expertise in environmental monitoring, water testing, microbiological methods, and contamination control
Solid knowledge of cGMP, microbiological best practices, and laboratory data systems such as LIMS
Experience with laboratory investigations, deviations, CAPAs, and technical documentation
Excellent analytical and organizational skills with the ability to work independently
Fluent in English and French (written and spoken)
What We Offer
6-month contract with an immediate start
Full-time position (40 hours per week)
Opportunity to work in a modern, highly regulated pharmaceutical laboratory
Collaborative international environment with experienced laboratory professionals jid0443eddait jit0727ait jpiy26ait