product development lifecycle within the medical device industry. This position collaborates closely with cross-functional... experience with medical device product development processes under FDA 21 CFR Part 820 and ISO 13485. Proficiency in 3D CAD...
product development lifecycle within the medical device industry. This position collaborates closely with cross-functional... experience with medical device product development processes under FDA 21 CFR Part 820 and ISO 13485. Proficiency in 3D CAD...
, etc.) and ensures documentation is complete and audit ready. Design History File (DHF) & Product Development Support: Reviews... and ensures completeness, accuracy, and regulatory compliance of DHFs throughout the product development lifecycle. Provides...
) & Product Development Support: Reviews and ensures completeness, accuracy, and regulatory compliance of DHFs throughout the... product development lifecycle. Provides quality engineering input during design reviews, risk management (ISO 14971...