CQV Specialist: Validate, Document & Optimize GMP Systems

Cencora seeks a CQV Consultant to deliver technical support for Commissioning, Qualification, and Validation activities. Located in Aguadilla, Puerto Rico, you will be responsible for managing CQV documents, developing protocols, and maintaining project schedules.

Ideal candidates will have a Bachelor's degree in Engineering or a Scientific field, with over 5 years' experience in regulated industries and a strong understanding of cGMP/FDA regulations. This position requires strong organizational skills and the ability to work independently.