Sr. Supplier Quality Engineer II – Medical Device

Grove Technical Resources; Grand Rapids (MI); On-site; USD 55,000 - 83,000; Full time

Job summary

Grove Technical Resources seeks a Sr. Supplier Quality Engineer II to oversee supplier quality operations for a medical device manufacturer in Grand Rapids, MI.

This onsite, W2 contract role spans 12+ months, focusing on driving supplier quality improvements, CAPAs, and compliance activities. The ideal candidate has 4+ years in supplier/manufacturing/medical device quality engineering, with hands-on problem solving and experience in GMP/QMS environments.

Qualifications

• 4+ years in Supplier Quality, Manufacturing Quality, or Medical Device Quality Engineering.
• Experience with GMP compliance and CAPA processes.
• Strong problem-solving and cross-functional collaboration.

Responsibilities

• Drive supplier quality improvements and performance monitoring.
• Investigate supplier-related quality issues and implement CAPAs.
• Support supplier audits and GMP compliance activities.
• Partner with Engineering, Operations, and Quality teams to resolve complex issues.
• Ensure suppliers consistently deliver quality materials, parts, and services.

Skills

Supplier quality management

Root cause analysis

CAPA

Nonconformance & deviation management

GMP compliance

Change control

QMS

Hands-on problem solving

Tools

TrackWise

Job description

Hiring: Sr. Supplier Quality Engineer II – Medical Device

Location: Grand Rapids, MI (Onsite)

Type: W2 contract

Duration: 12+ Months

We are seeking an experienced Sr. Supplier Quality Engineer II to support supplier quality operations for a leading medical device manufacturer in Grand Rapids, MI.

Key Skills Required:

• Supplier Quality Management & Supplier Performance Monitoring
• Root Cause Analysis, CAPA, Nonconformance & Deviation Management
• Quality Systems & Regulatory Compliance (GMP, Change Control, QMS)
• TrackWise or similar Quality Management Systems
• Hands-on Product Problem Solving in a Manufacturing Environment
• Mechanical, Industrial, Operations, or Biomedical Engineering Background

Preferred:

• Lean Six Sigma Yellow Belt or Green Belt Certification.

Experience:

• 4+ years in Supplier Quality, Manufacturing Quality, or Medical Device Quality Engineering.

Responsibilities:

• Drive supplier quality improvements and performance monitoring
• Investigate supplier-related quality issues and implement CAPAs
• Support supplier audits and GMP compliance activities
• Partner with Engineering, Operations, and Quality teams to resolve complex issues
• Ensure suppliers consistently deliver quality materials, parts, and services.