Manufacturing Validation Engineer / Pharmaceutical

Job Title: Manufacturing Validation Engineer / PharmaceuticalDuration: 6 MonthsLocation: Topeka Kansas 66603Job Type: Temporary AssignmentWork Type: RemoteWork Locations: Indianapolis IN, Kansas City KS, St. Louis MO, Columbus OHPay Rate : $ 59.20-59.20/ HrOverview TekWissen® is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. The below job opportunity is to one of Our clients who is a global leader in analytical testing, deliver a comprehensive portfolio of complete solutions - systems, software, consumables, and on-site and online services - with one overarching purpose: to help make the world healthier, cleaner, and more sustainable. 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. Depth of Experience:Mid to Senior level (typically 3–10+ years in CQV within Job pharmaceutical manufacturing) Commissioning & Qualification (C&Q) TekWissen® Group is an equal opportunity employer supporting workforce diversity.