Roles & Responsibilities:Quality Engineer withs strong medical device experience and PRODUCT QUALITY. MUST have experience with Class III/Implantable medical device(s).Experience maintaining/working within an ISO 13485 Quality Management System (QMS)Experience with CAPA Process.CE Marking experience.Good team player works cross functionally with Engineering and Quality.Solid understanding of regulatory standards & requirements (13485, MDR and FDA).Experience managing Quality Management System documents and systems.
Job Details
| ID | #53395559 |
| State | Michigan |
| City | Ypsilanti |
| Job type | Contract |
| Salary | USD TBD TBD |
| Source | Katalyst Healthcares & Life Sciences |
| Showed | 2025-02-04 |
| Date | 2025-02-04 |
| Deadline | 2025-04-05 |
| Category | Et cetera |
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