QC Analyst Microbiology (M/F/D)
Tasks:
1. Perform and approve QC analyses according to cGMPs, SOPs, and pharmacopoeias.
2. Enter results into management systems and address non-conformities promptly.
3. Manage and maintain laboratory equipment, including calibration and maintenance.
4. Ensure compliance with 5S standards and EHS rules.
5. Maintain accurate documentation (logbooks, forms) in compliance with GMP.
6. Prepare quarterly and annual trend reports and review invalid results.
7. Coordinate with suppliers for equipment maintenance and troubleshooting.
8. Collaborate with external labs and internal departments to ensure compliance.
Qualification:
1. CFC in microbiology or equivalent in the pharmaceutical/biotech industry.
2. Minimum 2-5 years of experience in a cGMP laboratory.
3. 2-5 years of experience in a cGMP laboratory or at least 2 years as Analyst I.
4. Minimum 5 years of experience in a cGMP laboratory or at least 5 years as Analyst II.
5. Strong understanding of laboratory methods, cGMPs, and Data Integrity principles.
6. Proficiency in handling laboratory equipment and systems.
7. Proficient in French and technical English (B2 minimum).
Requirements:
Start: 03.03.2025
Duration: 2 months or 5 months
Capacity: 5 days per week
Location: Neuchatel, Switzerland
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