The Process Development Engineer at ProQuality Network in Puerto Rico supports the development, validation, and implementation of new manufacturing processes within the medical devices industry. You will lead IQ/OQ/PQ activities, develop validation protocols, and collaborate across functions to mature concepts into scalable production.
Ideal candidates bring 5–7+ years in manufacturing/quality engineering, strong 21 CFR Part 820, GMP, and ISO 13485 knowledge, and hands-on experience with DOE,
#J-18808-LjbffrMedical Device Process Development Engineer (Contract) in pr at Unknown Company
This position is listed as full time and onsite.