Quality Manager – Sterile Manufacturing

French-Speaking Switzerland | GMP | Quality & Compliance

Looking for more visibility, responsibility and impact in Quality?

Join a specialized sterile pharmaceutical manufacturing site where you will work closely with Production, QA, QC and the Qualified Person, driving GMP compliance and operational quality activities in a highly regulated environment.

__Your 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 strong shopfloor presence and drive continuous improvement
• Act as compliance contact for customers and external partners
• Support inspections and client audits

Your Profile

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

__What’s on Offer?__

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