CQV Specialist: Validation & Commissioning Expert
Salas O'Brien, Inc.
Salas O’Brien is seeking a CQV Specialist to lead commissioning and validation activities in Columbus, OH. You will develop CQV Master Plans, conduct cGMP audits, and interface with OEMs, CMs, and contractors to execute CQV protocols. The role requires a Bachelor’s in engineering or science and 5–7 years of FDA-regulated experience. You’ll guide a team, manage multiple projects, and ensure compliance with GAMP, FDA cGMPs, and Good Engineering Practices. #J-18808-Ljbffr Salas O'Brien, Inc.
Vacancy posted 4 days ago
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