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QC Analyst Microbiology (M/F/D)
Tasks:
Conduct and approve QC analyses following cGMPs, SOPs, and pharmacopoeias.
Ensure adherence to Good Manufacturing and Documentation Practices (GMP/GDP).
Maintain and calibrate laboratory equipment; manage 5S standardization.
Oversee equipment logbooks and ensure real-time Kanban management.
Complete forms, logbooks, and trend reports; address non-conforming results.
Train analysts on equipment use; serve as a backup trainer for GMP.
Support and lead continuous improvement initiatives and GEMBAs.
Supervise results from external labs and collaborate on analysis approvals.
Qualification:
Minimum CFC in microbiology or equivalent experience in the pharmaceutical/biotech industry.
2-5 years of experience in a cGMP laboratory or at least 2 years as Analyst I; minimum 5 years for Analyst II
Strong knowledge of laboratory methods and cGMPs.
Expertise in Data Integrity principles and laboratory system
Proficient in French and technical English (B2 minimum).
Skilled with standard IT tools (e.g., MS Office) and laboratory management systems.
Requirements:
Start: 15.01.2025
Duration: 5 months
Capacity: 5 days per week
Location: Neuchatel, Switzerland
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