Quality Manager – Sterile Manufacturing

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 jpida27bbd0jm jpit0936jm jpiy26jm