A growing medical device company in Minneapolis is seeking a hands-on Director of Post-Market Quality to own all post-market activities for its Class III devices — including complaints, CAPA, vigilance, and trend analysis.

A high number of candidates may make applications for this position, so make sure to send your CV and application through as soon as possible.

This on-site role is ideal for someone who loves being in the details, wearing many hats, and building systems from the ground up. You’ll partner closely with engineering, regulatory, and operations to drive compliance and continuous improvement.

What You’ll Bring: Experience with post-market quality for Class III medical devices Deep knowledge of complaint handling, CAPA, and regulatory requirements Engineering degree preferred, but not required A proactive, roll-up-your-sleeves approach No direct reports to start, but growth and leadership opportunities ahead.

Ready to make an impact in a fast-growing med device environment? Let’s talk.