{"id":3905753,"url":"https://alion.io/job/bachem-senior-specialist-qa","title":"Senior Specialist QA","company":{"id":1821024,"name":"Bachem","domain":"bachem.com","url":"https://alion.io/company/bachem","size_band":"501-1000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"SuccessFactors","truth_index":null},"role":"QA","role_family":"QA","seniority":"senior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Vionnaz, Switzerland"],"countries":["CH"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false},{"name":"GMP","optional":false}],"status":"live","first_seen_at":"2026-11-07T03:02:55Z","employer_posted_date":"2026-11-06","last_verified_at":"2026-11-10T13:37:37Z","board_verified":true,"closed_at":null,"days_open":3,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":3},"description":"To strengthen our Quality Assurance team at our Vionnaz production site, we are looking for a Senior Specialist QA - Operations (a) 100%. In this role, you will help ensure GMP compliance across manufacturing activities while acting as a key quality partner for operational teams and site projects.\nYour Responsibilities\nCoordinate and perform batch release activities for finished products and intermediates.\nReview and approve quality events, root cause analyses, CAPAs, and effectiveness checks.\nSupport and approve laboratory investigations.\nAssess, coordinate, and approve change requests.\nReview and approve master manufacturing documentation.\nApprove qualification protocols and reports for facilities and equipment.\nConduct internal and external audits and support customer and regulatory inspections.\nRepresent Quality Assurance in site projects and contribute to SOP creation and revision.\nYour Profile\nMaster’s degree in Engineering, Chemistry, Pharmacy, or a related field.\nMinimum 5 years of experience in the pharmaceutical or chemical industry; QA Operations experience is highly desirable.\nStrong knowledge of GMP requirements and their practical application in a manufacturing environment.\nAbility to independently assess issues, make sound decisions, and appropriately escalate risks.\nSolution-oriented mindset with a strong customer and service focus.\nExcellent organizational and communication skills.\nFluent in French and English, both written and spoken.\nGerman language skills are considered an asset.\nOur offer\nA modern and dynamic working environment within a fast-growing international company.\nChallenging projects of high scientific and technical value.\nOpportunities for professional development and continuing professional development.\nA corporate culture based on collaboration, innovation and excellence.\nAttractive working conditions and competitive employee benefits.\nInterested\nWould you like to drive innovation together with us?\nWe look forward to receiving your complete application documents via our application portal.\nLearn more about the Bachem Group and get inspired 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