Princeton, NJ30+ days ago
This leader will oversee process improvements for the end-to-end processes of complaint intake, investigation quality, medical device reportability (vigilance), complaint closure, health hazard evaluations, post-market surveillance, and signal detection across two businesses consisting of a diverse portfolio of leading medical devices. + Partner with Regulatory, Clinical, Medical Safety, R&D, and Supply Chain to ensure embedding of complaint signals into CAPA, risk management (ISO 14971), design controls , and production controls (e.g., ISO 13485 / 21 CFR Part 820 / Part 4 for combination products as applicable).