H2French-Speaking Switzerland | GMP | Quality Compliance /h2 pLooking for more visibility, responsibility and impact in Quality? /p pJoin 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. /p pstrongYour Responsibilities /strong /p ul liSupport batch review and release activities /li liReview GMP documentation and manufacturing records /li liManage deviations, CAPAs and Change Controls /li liProvide quality support to production, laboratories and warehouse operations /li liMaintain strong shopfloor presence and drive continuous improvement /li liAct as compliance contact for customers and external partners /li liSupport inspections and client audits /li /ul pYour Profile /p ul liDegree in Pharmacy, Chemistry, Life Sciences or Engineering /li liExperience in GMP-regulated pharmaceutical manufacturing /li liStrong exposure to sterile / aseptic production /li liExperience with deviations, investigations and Change Controls /li liOperational mindset and willingness to work close to production /li liFluent French and good English /li /ul pstrongWhat’s on Offer? /strong /p ul liHigh visibility role within a specialized pharmaceutical manufacturing site /li liBroad quality responsibilities with direct impact on operations /li liClose collaboration with Production, QA, QC and Release teams /li liInternational environment with short decision paths /li liExcellent opportunity to further develop towards broader Quality and QP responsibilities /li /ulbrpgloorlang THE RIGHT CHOICE IN CONSULTATION FOR LIFE SCIENCE TALENTS /p