Junior QC Analyst (m/f/d)

Tasks :

• Perform and approve analytical results in the QC laboratory according to SOPs, cGMP, and applicable standards.

• Ensure compliance with Good Documentation Practices and accurately complete forms, logbooks, and electronic systems.

• Identify and report non-conforming or invalid results immediately, initiating quality system events as required.

• Execute reagent/consumable qualifications, method, system, and equipment validation protocols.

• Maintain laboratory organization, adhere to 5S standards, and ensure proper equipment calibration and maintenance.

• Support continuous improvement initiatives, GEMBAs, HOP, and troubleshooting of minor issues.

• Train analysts on equipment and procedures, acting as a backup GMP trainer when needed.

• Manage and review equipment logbooks, and support vendor maintenance or unplanned interventions.

• Participate in deviation management, risk analyses, trend reports, and inspections/audits.

• Act as subject matter expert (SME) for projects, regulatory submissions, and corrective/preventive actions.

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 in a cGMP laboratory or 5 years as Analyst II.

• Good to very good knowledge of laboratory methods.

• Good knowledge of cGMP.

• Knowledge of Data Integrity principles, with advanced knowledge preferred.

• Proficient in standard IT tools (MS Office).

• Fluent in French and English (technical).

• English level B2 minimum.

Start : 22.09.2025