Supplier Quality Engineer III

JCW Group; Maple Grove (MN); Hybride; USD 69 000 - 76 000; Plein temps

Résumé du poste

JCW Group in Maple Grove, MN is seeking a Supplier Engineer III for a hybrid role combining on-site collaboration Tue-Thu with remote work. This contract position runs 12 months and starts late November, offering exposure to high-impact supplier quality remediation in medical devices.

You will lead PFMEA remediation, validate supplier processes, and coordinate with contract manufacturers and cross-functional teams to ensure patient safety and product quality.

Qualifications

• 2-5 years of experience in a manufacturing environment.
• Hands-on validation and change management experience.

Responsabilités

• Review, remediate, and approve supplier PFMEAs against newly defined criteria.
• Review and approve supplier process and inspection validations against statistical requirements.
• Lead change management activities to close gaps in supplier documentation.
• Partner with suppliers and internal cross-functional teams to drive deliverables to completion.
• Uphold a strong commitment to patient safety and product quality in every step.

Connaissances

Project management

Supplier quality

Validation

Six Sigma

Outils

IQ/OQ/PQ

TMV

Description du poste

Supplier Engineer III | Medical Device | Maple Grove, MN (Hybrid)

Contract: 12 months, starting late November

Pay: $50-55/hr

Schedule: Hybrid, onsite Tuesday through Thursday

Travel: Up to 15% domestic

About the opportunity

A global medical device manufacturer is looking for a Supplier Engineer to lead a high-visibility quality remediation project. You'll work directly with contract manufacturers that build finished medical devices, making sure their process risk documentation and validations meet updated company standards. This role suits an engineer who likes owning a project, working with suppliers, and seeing measurable results.

What you'll do

• Review, remediate, and approve supplier PFMEAs against newly defined criteria
• Review and approve supplier process and inspection validations against statistical requirements
• Lead change management activities to close gaps in supplier documentation
• Partner with suppliers and internal cross-functional teams to drive deliverables to completion
• Uphold a strong commitment to patient safety and product quality in every step

What you bring

• 2-5 years of experience in a manufacturing environment
• Hands-on validation and change management experience

Nice to have

• Medical device industry experience
• Supplier quality or supply chain experience
• IQ/OQ/PQ and test method validation (TMV) experience
• Working knowledge of statistical methods and Six Sigma tools
• Strong communication and project management skills

Why this role

• Build deep supplier quality and validation experience at a leading med device company
• Clear project scope with real impact on product quality
• Defined hybrid schedule in the Twin Cities