CQV Engineer
United Pharma
We are seeking a CQV Engineer to support commissioning, qualification, and startup activities within a biologics manufacturing facility. This hands‑on role focuses on validation execution, equipment startup, troubleshooting, and GMP documentation in a fast‑paced pharmaceutical environment. Key Responsibilities Author, review, and execute IQ/OQ/PQ validation protocols and reports. Support equipment commissioning, startup, system walkdowns, and operational readiness. Troubleshoot bioprocess equipment and resolve field execution issues. Collaborate with Engineering, Quality, Automation, and Operations teams. Complete deviations, validation documentation, and GMP records. Support commissioning activities using CMMS/work orders and ensure compliance with GMP standards. Qualifications Bachelor's degree in Engineering or related technical field. 1–5+ years of CQV, Validation, or Biotech/Pharmaceutical Manufacturing experience. Experience with bioreactors, pumps, or large stainless‑steel process equipment. Strong knowledge of IQ/OQ/PQ execution, GMP documentation, and equipment troubleshooting. Experience with Kneat, Chromatography, UF/DF, or startup/commissioning environments is a plus. #J-18808-Ljbffr United Pharma
Vacancy posted 3 days ago
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