Quality Manager – Sterile Manufacturing

Job description

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