Medical Device Manufacturing Professional
This role involves the day-to-day production of medical devices. Key responsibilities include building sub-assemblies and finished devices, conducting visual and dimensional inspections, and managing materials on the manufacturing line.
The ideal candidate will have relevant industry experience and a strong understanding of quality management systems. This includes ISO 13485, FDA regulations, and EU directives.
Main Responsibilities:
1. Build sub-assemblies and finished devices for testing, clinical investigations, and commercial release.
2. Conduct part and subassembly visual and dimensional inspection activities in accordance with documented procedures and standards.
3. Manage materials on the manufacturing line, including issuing parts and setting up equipment and fixtures.
4. Participate in training activities and become proficient in required manufacturing and inspection activities.
5. Assist with