Description
EQVAL Group is hiring a full-time Manufacturing Engineer to work 100% on site in Dorado, Puerto Rico. The role focuses on executing IQ, OQ, and PQ validation activities, developing validation documentation, troubleshooting and optimizing manufacturing processes, supporting NCR, complaint, and CAPA investigations, and maintaining cGMP compliance. Candidates need a bachelor’s degree in engineering, at least three years of experience in medical device or pharmaceutical manufacturing, validation and quality-system experience, bilingual English and Spanish proficiency, and strong technical writing skills. Benefits include medical, dental, vision, and pharmacy insurance, life insurance, paid time off, holidays, professional development, a referral program, and a productivity incentive.
