Senior CQV Validation Engineer – GMP & Sterilization Expert

A service provider company in engineering seeks a qualified C&Q Engineer for its Operations in Juncos, Puerto Rico. The ideal candidate should have a Bachelor's degree with at least eight years of experience in the pharmaceutical industry, bilingual in English and Spanish, and strong project management skills. Responsibilities include reviewing validation documents, supporting testing execution, and participating in design phases. Join a flexible, family-oriented company committed to well-being and quality talent. #J-18808-Ljbffr