{"id":3624060,"url":"https://alion.io/job/nemensis-ag-qualification-validation-engineer-mwd","title":"Qualification & Validation Engineer (m/w/d)","company":{"id":4494637,"name":"Nemensis","domain":"nemensis.com","url":"https://alion.io/company/nemensis-ag","size_band":null,"is_staffing_agency":true,"employer_type":"agency","is_intermediary":false,"listed_via":"myjob.ch","ats_vendor":null,"truth_index":null},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Lucerne, 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":"2026-11-02T19:19:29Z","employer_posted_date":"2026-11-02","last_verified_at":"2026-11-02T19:19:29Z","board_verified":false,"closed_at":null,"days_open":7,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":7},"description":"Qualification & Validation Engineer (m/w/d)\n Shape the Future of Pharmaceutical Quality (m/w/d)\n Assignment period: 01.12.2026 - 30.11.2027\n Location: Schachen (LU)\n Employment type: Temporary placement\n For our client, a globally active pharmaceutical company running a high-tech development site in the Lucerne region, we are looking for a Qualification & Validation Engineer (m/w/d) who thrives under strict GMP standards.\n Your tasks\n Own qualification and validation projects for lab instruments, equipment, clean rooms, utilities and facilities\n Draft, review and execute validation documents such as protocols, reports and risk assessments\n Oversee computer system validation (CSV) across manufacturing and quality areas\n Ensure compliance with cGMP guidelines and regulatory expectations\n Liaise with Production, Quality Control and Engineering on validation topics\n Support internal and external audits and inspections\n Review GMP documents incl. deviations, CAPAs and change controls\n Your profile\n Degree in engineering, pharmacy, chemistry, biotechnology, microbiology or related field\n 5+ years of hands-on experience in qualification and validation, incl. CSV\n Solid grasp of GMP/cGMP principles and regulatory expectations\n Analytical mindset with strong documentation and problem-solving skills\n Comfortable working independently and in cross-functional teams\n Fluent in English and German (min. B1)\n Familiarity with GAMP5, Annex 11/15 and data integrity is a plus\n What nemensis offers you\n Nemensis AG is your specialised recruitment partner for Life Sciences, based in Basel\n Comprehensive guidance and support throughout the application process provided by our consultants\n Access to a broad network of clients and exciting positions across north-western Switzerland\n Fast and straightforward onboarding thanks to individual coaching and advice during the application process\n At nemensis ag, we've already connected thousands of candidates with their dream job. Ready for the role of Qualification & Validation Engineer (m/w/d) in Schachen (LU)? Get in touch with us!\n ? 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