Validation Specialist: PV/CSV (GMP, Medical Devices)

A leading consulting firm located in Puerto Rico and the USA is seeking a motivated individual to perform process validation and equipment qualification within the pharmaceutical manufacturing sector. Candidates should have a Bachelor's degree in Science, at least 2 years of related experience, and a solid understanding of GMP documentation and risk management. Fluid availability for shifts, including overtime, is necessary as the role demands flexibility in a dynamic environment. #J-18808-Ljbffr