Quality Assurance Manager

6 days ago


Ponte Vedra, United States Treace Full time
About the Role

We are looking for an experienced Principal Design Quality Engineer to lead and support key strategic projects, new product development, and provide quality oversight to the R&D organization.

In this role, you will work closely with cross-functional teams to ensure products meet quality standards consistent with internal procedures and acceptance criteria, while meeting all design control and other regulatory requirements.

The ideal candidate will have a strong background in medical device engineering, with a minimum of 7 years of experience working within an FDA compliant Title 21 section 820 environment.

The estimated salary for this position is around $125,000 - $155,000 per year, based on experience and qualifications.

Main Responsibilities:
  1. Provide Quality oversight and approval of qualification/validation/design control activities.
  2. Collaborate with Surgeon Advisory Board, Marketing, and Design Engineers on new product feasibility.
  3. Review and assess the quality and technical rigor for manufacturability (DFM) of new product designs.

Treace is a drug-free employer and is committed to maintaining a safe and healthy work environment.



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