{"id":3154213,"url":"https://alion.io/job/randstad-sourceright-cqv-engineer","title":"CQV Engineer","company":{"id":2632310,"name":"Randstad Sourceright","domain":"talent-pool.com","url":"https://alion.io/company/talent-pool","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"TalentPools","truth_index":{"grade":"B","score":75,"open_postings":111,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":45,"computed_at":"2026-10-25T05:49:26Z"}},"role":"Biotech","role_family":"Biotech","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":["Visp, 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}],"status":"live","first_seen_at":"2026-10-23T10:49:19Z","employer_posted_date":"2026-10-23","last_verified_at":"2026-10-25T13:44:16Z","board_verified":true,"closed_at":null,"days_open":2,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":2},"description":"Are you a Quality and Commissioning specialist ready to make an immediate impact on life-saving pharmaceutical manufacturing? Join our team in Visp as a CQV Engineer, where you will ensure our state-of-the-art facilities and equipment meet the highest GxP compliance standards.\nThis is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.\nWhat you will get:\nAn agile career and dynamic working culture.\n\nAn inclusive and ethical workplace.\n\nCompetitive hourly rate.\n\nWhat you will do:\nDrive end-to-end qualification and requalification activities (DQ, IQ, OQ, PQ phases) for technical equipment and facilities (such as freezers, washing machines, and unit operations) across their full lifecycle.\n\nPlay a key role in maintaining compliance across operational transitions, ensuring seamless adaptation to our new Document Management System (AVIVA).\n\nPrepare, process and coordinate Technical Change Requests (TCRs) and maintain continuous oversight of the qualified state of all assigned systems.\n\nLead deviation management, root cause investigations, and CAPA implementations to safeguard quality and regulatory compliance.\n\nServe as the Subject Matter Expert (SME) for CQV, providing technical guidance and coaching to cross-functional teams across Operations, Betriebsengineering, and QA.\n\nAuthor, review, and approve GxP-compliant technical documentation using Kneat, SAP, and COMOS.\n\nRepresent the CQV department as a key technical expert during internal and external quality audits, customer visits, and regulatory inspections.\n\nWhat we are looking for:\n5 to 10 years of proven experience in pharma, biotech, or CDMO environments governed by strict GxP regulations.\n\nStrong practical background in Commissioning, Qualification, and Requalification (DQ/IQ/OQ/PQ) of pharma manufacturing equipment and utilities.\n\nTechnical degree (HF/FH/University in Applied Sciences or Engineering) or equivalent hands-on technical experience in a relevant industry.\n\nProfessional fluency in German and English is required\n\nProficiency in GxP documentation platforms and software tools, specifically Kneat, SAP, COMOS, MS Word, Excel, and PowerPoint.\n\nDemonstrated ability to work independently with high attention to detail, proactive problem-solving skills, and strong cross-functional communication abilities.\n\nAbout Lonza\nAt Lonza, their people are their greatest strength. With 30+ sites across five continents, their globally connected teams work together every day to manufacture the medicines of tomorrow. Their core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who they are and how they work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work they want you to be part of.\nInnovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, they value diversity and are committed to creating an inclusive environment.\nAs Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role.\nReady to play your part in shaping the future of life sciences? 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