Supplier Engineer III — Medical Device (Hybrid - Maple Grove, MN) Contract - Possible Temp to Hire

Our Medical Device client has an exciting opportunity for a Supplier Engineer III.

Job Summary:

This Supplier Engineer (SE) will be responsible for the remediation activities identified by CAPA 7720 for client’s contract manufactured (CM) sourced finished medical device (SFMD) product. This individual works independently, serves as a leader for SE remediation activities, and interacts cross-functionally with client's team members and CM SFMD suppliers to execute deliverables according to business needs.

Responsibilities and Job Requirements:

1. Review, remediate, and approve CM SFMD supplier’s process risk documentation (PFMEA) to newly defined criteria.

2. Review, remediate, and approve CM SFMD supplier’s process and inspection validations to client’s statistical requirements.

3. Perform change management activities to remediate gaps found in CM SFMD Supplier’s process risk documentation and process/inspection validations.

4. Collaborate with CM SFMD suppliers and client’s functional resources to complete all activities needed to approve supplier’s process risk documentation and process/inspection validations to the newly defined criteria.

5. In all actions, it demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.

Other Details:

• Schedule: 40 hours

• Contract Length: 12 months (Possible temp to hire)

• Work Set-Up: Hybrid in Maple Grove, MN

• Start Date: 11/23/2026

• Travel Requirements: Ability to travel up to 15% of the time. (Domestic possible.)