Ph3French-Speaking Switzerland | GMP | Quality Compliance /h3pLooking for more visibility, responsibility and impact in Quality? /ppJoin 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. /ph3Your Responsibilities /h3ulliSupport batch review and release activities /liliReview GMP documentation and manufacturing records /liliManage deviations, CAPAs and Change Controls /liliProvide quality support to production, laboratories and warehouse operations /liliMaintain strong shopfloor presence and drive continuous improvement /liliAct as compliance contact for customers and external partners /liliSupport inspections and client audits /li /ulh3Your Profile /h3ulliDegree in Pharmacy, Chemistry, Life Sciences or Engineering /liliExperience in GMP-regulated pharmaceutical manufacturing /liliStrong exposure to sterile / aseptic production /liliExperience with deviations, investigations and Change Controls /liliOperational mindset and willingness to work close to production /liliFluent French and good English /li /ulh3What’s on Offer? /h3ulliHigh visibility role within a specialized pharmaceutical manufacturing site /liliBroad quality responsibilities with direct impact on operations /liliClose collaboration with Production, QA, QC and Release teams /liliInternational environment with short decision paths /liliExcellent opportunity to further develop towards broader Quality and QP responsibilities /li /ul /p #J-18808-Ljbffr