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Validation & Engineering Group, Inc. seeks a CIP/COP CQV Lead with 13-14+ years of experience. The SME will lead CIP/COP systems, from design through verification, and provide technical direction for project execution.
Role requires strong leadership, regulatory awareness (FDA, GMP), and the ability to coordinate cross-functional teams in fast-paced pharmaceutical environments.
Current job opportunities are posted here as they become available.
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
We are seeking a CIP/COP CQV Lead with a minimum of 13-14+ years of relevant experience. The ideal candidate will be a Subject Matter Expert (SME) in Clean-in-Place (CIP) and Clean-out-of-Place (COP) systems. They should have strong experience with CIP/COP equipment, cleaning processes, system design, commissioning, qualification, and verification. The individual in this role must be capable of independently leading the CIP/COP node, providing technical direction, and coordinating execution activities.
At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.