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

Pharmavise Corporation • Maple Grove, MN

3d • Hybrid

About The Position

The Supplier Engineer III is responsible for remediation activities identified by CAPA 7720 for contract-manufactured, supplier-sourced finished medical device products. The role works independently, leads supplier engineering remediation activities, and collaborates with internal cross-functional team members and suppliers to complete deliverables according to business needs.

The position reviews, remediates, and approves supplier process risk documentation (PFMEA) and process and inspection validations against newly defined criteria and statistical requirements. It also performs change management to address identified gaps and collaborates with suppliers and internal functional resources to complete the necessary activities for approval. The role maintains a primary commitment to patient safety and product quality while complying with the Quality Policy and documented quality processes and procedures.

This is a 12-month contract with possible temp-to-hire conversion. The schedule is 40 hours per week, with a hybrid work setup in Maple Grove, Minnesota, and domestic travel of up to 15% may be required. The stated start date is November 23, 2026.

Requirements

• Bachelor’s degree in engineering.
• 2–5 years of experience in a manufacturing environment.
• Ability to travel up to 15% of the time; domestic travel is possible.
• Problem-solving abilities.
• Manufacturing experience.
• Validation experience.
• Change management experience.

Nice To Haves

• Experience working with suppliers or in supply chain management.
• Experience working in the medical device field.
• Experience with installation qualifications (IQ), operational qualifications (OQ), performance qualification (PQ), and test method validation (TMV).
• Excellent communication and project management skills.
• Strong bias for action and results orientation.
• Self-driven and self-motivated to learn and apply knowledge to produce results.
• Good understanding of statistical methods, Six Sigma methodologies, and problem-solving methodologies.

Responsibilities

• Review, remediate, and approve contract-manufactured, supplier-sourced finished medical device suppliers’ process risk documentation (PFMEA) to newly defined criteria.
• Review, remediate, and approve supplier process and inspection validations to the client’s statistical requirements.
• Perform change management activities to remediate gaps in supplier process risk documentation and process or inspection validations.
• Collaborate with suppliers and the client’s functional resources to complete activities needed to approve supplier process risk documentation and process and inspection validations to newly defined criteria.
• Maintain a primary commitment to patient safety and product quality by complying with the Quality Policy and documented quality processes and procedures.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level