Operational Quality Assurance Coordinator (M/F)

Manpower Life Science, a recruitment firm specializing in the healthcare industries, supports its clients in their strategic recruitment and development projects.

We are looking for an Operational Quality Assurance Engineer / Operational QA Pharmacist (M/F) for a 6-month temporary mission, renewable for another 6 months, to join a pharmaceutical site located in Saint-Julien-en-Genevois (74).

Start date: As soon as possible. Reporting to the Quality Assurance Manager, you will ensure quality support for Production and Quality Control activities in a context of growth and the relaunch of strategic projects at the site.

Your main missions:

• Support Production and Quality Control teams in the application of GMP requirements and good quality practices.
• Manage deviations, participate in investigations, root cause analyses, and the follow-up of CAPA.
• Contribute to the management of Change Control related to site processes, equipment, and activities.
• Perform batch record reviews and verify the GMP compliance of documents, critical data, and identified discrepancies.
• Participate in analytical method validation activities and the review of associated protocols and reports.
• Intervene in the qualification and validation activities of laboratory and production equipment.
• Ensure quality follow-up of actions resulting from validations, qualifications, and Quality Control projects.
• Participate in the drafting and updating of quality documentation.
• Contribute to internal audits, the preparation of regulatory inspections, and continuous improvement processes.

You will evolve within a dynamic Quality Assurance team and actively participate in the site's development and compliance projects.

• Pharmacist, Engineer, or holder of a Master 2 in Quality, Bioprocesses, or Life Sciences.
• First experience in Quality Assurance within a pharmaceutical or biotechnological environment subject to GMP.
• Experience in analytical method validation and equipment qualification.
• Experience in deviation management, CAPA, Change Control, and quality document review is appreciated.
• Mastery of GMP standards is indispensable.
• Professional written English required for the review of validation protocols and reports.
• Rigor, autonomy, analytical mindset, and a taste for teamwork.

?Conditions

• 6-month temporary mission, renewable for 6 months.
• Executive status (Cadre).
• Remuneration: 40 to 43 K€ gross/year.
• Approximately 15 RTT per year.
• 1 day of teleworking per week (excluding Monday and Friday).
• Position based in Saint-Julien-en-Genevois (74).

As part of its diversity policy, Manpower considers all applications, including those from people with disabilities, provided they have equal skills.

Contract: Temporary mission

Experience: 2 years

Salary: 40,000 to 43,000 € per year

Start date: As soon as possible

Duration: 6 months renewable

Additional information: operational