I'm working with a start-up Medical Device company who is looking to bring on a Senior Quality Systems member to the their Quality team.
Role Description and Requirements:
- Building out and managing the company eQMS
- provide quality related trainings
- Plan, coordinate, and conduct scheduled internal audits to assess compliance
- Familiar with FDA regulations and ISO 13485, 21 CFR, and EU MDR
- 5-10 years of experience with Quality Systems within the Medical Device Industry
Please note: this role can be offered at the Senior level, Supervisor, or Manager level!