CQV Engineer — Equipment Validation & Commissioning Pro

A leading EPCM firm is looking for a CQV Engineer to support equipment validation at a client in New Bedford, MA. The ideal candidate will have 3-5 years of experience in a cGMP and FDA-regulated environment, with a solid understanding of equipment. Responsibilities include developing validation protocols, supporting resolution of issues, and ensuring quality in validation documentation. The position requires strong collaboration with client teams to ensure successful project execution.
#J-18808-Ljbffr