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 & regulatory knowledge
• Experience with systems like TrackWise/KNEAT is a plus
• Fluent English (German beneficial)

If this role is for you then contact dominic.pritchard@biotalent.ch