GMP QA Operations Lead (Sterile)– Onsite 3 Days/Week, Visp

QA Operations Expert– GMP (Sterile Manufacturing) | Stein, Switzerland 8 month contract 3 days per week onsite English speaking (+German is a bonus) We’re supporting a leading life sciences organisation in Stein in hiring an experienced

Quality Assurance professional

to oversee GMP compliance within sterile manufacturing. Key Responsibilities Act as QA single point of contact for assigned manufacturing activities Review&approve SOPs, deviations, CAPAs, change controls, validation docs Ensure GMP compliance across operations and support audits/inspections Drive investigations (root cause, impact, action plans) Support continuous improvement&quality system enhancements Collaborate with cross-functional teams and external partners Your Profile Degree in Chemistry, Biology, Pharmacy or similar 5–10 years QA/QC experience in pharma manufacturing Strong GMP®ulatory knowledge Experience with systems like TrackWise/KNEAT is a plus Fluent English (German beneficial) If this role is for you then contact

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