Sr. CQV Enginner (Indianapolis)

Job Title: Sr. CQV EngineerLocations: Indianapolis IN/Kansas City KSDuration: 6 monthsDepth 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.