{"id":2094828,"url":"https://alion.io/job/cai-cqv-engineer","title":"CQV Engineer","company":{"id":3866618,"name":"CAI","domain":"caiready.com","url":"https://alion.io/company/caiready","size_band":"501-1000","is_staffing_agency":false,"employer_type":"staffing","is_intermediary":false,"listed_via":null,"ats_vendor":"Lever","truth_index":{"grade":"D","score":53,"open_postings":80,"ghost_share":0.788,"stale_share":0,"repost_share":0,"time_to_fill_p50_days":null,"computed_at":"2026-10-13T05:45:00Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":null,"employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["Amsterdam, Netherlands","Dublin, Ireland"],"countries":["NL","IE"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":85000,"max":95000,"currency":"EUR","period":"year","gross":null,"usd_annual":106196},"salary_estimate":null,"experience_years_min":null,"visa_sponsorship":true,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-09-07T10:38:33Z","employer_posted_date":"2026-09-07","last_verified_at":"2026-10-13T09:30:19Z","board_verified":true,"closed_at":null,"days_open":35,"trust":{"level":"ok","repost_count":0,"flags":["company_stale"],"days_open":35},"description":"CAI is seeking experienced Commissioning, Qualification & Validation (CQV) Engineers to support a large scale pharmaceutical manufacturing project in the Netherlands. This role offers the opportunity to work within a multidisciplinary team delivering critical process, utility, and facility qualification activities in a GMP regulated environment.\nResponsibilities\nExecute commissioning and qualification activities for process, utility, and facility systems.\nDevelop, review, and execute qualification documentation in line with project and regulatory requirements.\nSupport system turnover, startup, and operational readiness activities.\nLiaise with engineering, quality, operations, and project stakeholders to ensure successful project delivery.\nParticipate in walkdowns, punch-list resolution, and troubleshooting activities.\nEnsure compliance with site quality, safety, and GMP procedures.\nExperience Required\nPrevious CQV experience within pharmaceutical, biotech, or life sciences manufacturing environments.\nStrong understanding of commissioning and qualification methodologies.\nExperience supporting regulated manufacturing facilities and associated utility systems.\nExposure to complex process equipment and containment-focused manufacturing operations is highly desirable.\nFamiliarity with GMP documentation, protocol execution, and project lifecycle delivery.\nPreferred Experience\nCandidates with experience in one or more of the following areas are particularly encouraged to apply:\nHigh containment or high potency manufacturing environments\nProcess equipment qualification\nManufacturing support systems and clean utilities\nHVAC and facility qualification\nPackaging, processing, or solid dosage manufacturing operations\nSafety critical or hazardous processing environments\nOther Requirements\nThis is a site-based role\nEligible to work in the EU without the need for visa sponsorship, now or in the future.\nWhy CAI?\nAt CAI, our people are at the heart of everything we do. We partner with the world's leading life sciences companies to deliver innovative projects that ultimately improve patient lives. 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