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Stark Pharma Solutions Inc. is seeking a CQV Engineer with strong experience in pharmaceutical manufacturing and regulated environments to support commissioning, qualification, and validation activities for facilities, utilities, equipment, and systems.
The role collaborates with Engineering, Quality, Manufacturing, and Project teams to develop, execute CQV protocols (IQ/OQ/PQ) and ensure compliance with GMP, FDA, and GxP requirements, while driving continuous improvement projects.
Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.
CQV Engineer
North Carolina
Long Term
We are seeking a CQV Engineer with strong experience in pharmaceutical manufacturing and regulated environments to support commissioning, qualification, and validation activities for facilities, utilities, equipment, and systems.
Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse backgrounds.