Sr. CQV Engineer
Stellar Consulting Solutions, LLC
Locations: Indianapolis IN/Kansas City KS (Onsite) Duration: 6 months (Contract to Hire) Depth of Experience: Mid to Senior level (typically 3–10+ years in CQV within pharmaceutical manufacturing) Job Description: Develop, execute, and document commissioning, qualification, and validation protocols (IQ/OQ/PQ) for new and modified equipment, utilities, and facilities. Author and review qualification documents, test scripts, deviation reports, and summary reports. Perform risk-based commissioning and qualification activities in accordance with FDA, EMA, and internal quality standards. Coordinate closely with engineering, quality assurance, validation, and operations teams throughout the C&Q lifecycle. Support technology transfer, process validation, and handover to manufacturing. Participate in deviation investigations, CAPA implementation, and continuous improvement of CQV processes. #J-18808-Ljbffr
Vacancy posted 7 hours ago
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