Supplier Engineer III — Medical Device (Hybrid - Maple Grove, MN) Contract - Possible Temp to Hire
- Hiring from
- United States
- Work type
- Hybrid
- Posted
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About Us
From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com and follow us on LinkedIn: https://www.linkedin.com/company/pharmavisecorp
Job Description
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.)
Requirements
Required Qualifications:
· Bachelor’s degree in engineering is required!
· 2-5 years of experience in a manufacturing environment.
· Ability to travel up to 15% of the time. (Domestic possible.)
· Problem solving abilities
· Mfg. experience
· Validation experience
· Change management experience
Preferred qualifications:
· 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 oriented.
· 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.
Pharmavise Corporation is an Equal Opportunity Employer and does not discriminate on the basis of race or ethnicity, religion, sex, national origin, age, veteran disability or genetic information or any other reason prohibited by law in employment.
