CQV Engineer: GMP Validation & Commissioning

IPS is seeking a CQV Engineer to support Commissioning, Qualification and Validation of technically complex facilities in life sciences. You will perform cGMP-compliance based C/Q/V services and may perform standalone commissioning for non-FDA regulated clients. Responsibilities include writing C/Q/V documents, witnessing FATs/SATs, and compiling data for reports. The role requires a Bachelor of Science in Engineering and 2+ years of related experience.