Quality Manager – Sterile Manufacturing

About the role

We are seeking a Quality Manager to join a specialized sterile pharmaceutical manufacturing site in French‑speaking Switzerland. You will work closely with Production, QA, QC and the Qualified Person to ensure GMP compliance and drive operational quality in a highly regulated environment.

Key responsibilities

• Support batch review and release activities.
• Review GMP documentation and manufacturing records.
• Manage deviations, CAPAs and Change Controls.
• Provide quality support to production, laboratories and warehouse operations.
• Maintain a strong shop‑floor presence and promote continuous improvement.
• Act as the compliance contact for customers and external partners.
• Support inspections and client audits.

Required profile

• Degree in Pharmacy, Chemistry, Life Sciences or Engineering.
• Experience in GMP‑regulated pharmaceutical manufacturing.
• Strong exposure to sterile/aseptic production.
• Hands‑on experience with deviations, investigations and Change Controls.
• Operational mindset with willingness to work close to production.
• Fluent French and good English.

Required skills

• GMP
• Sterile manufacturing
• Aseptic production
• CAPA management
• Change Control processes

What we offer

• High visibility role within a specialized pharmaceutical site.
• Broad quality responsibilities with direct impact on operations.
• Close collaboration with Production, QA, QC and Release teams.
• International environment with short decision paths.
• Opportunity to develop towards broader Quality and Qualified Person responsibilities.