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Together with our customers, we are driven to make healthcare better. #WeAreStryker
Staff Engineer, Supplier Quality Engineering
Location
Illinois
Posted
101 days ago
Salary
$98.2K - $163.7K / year
Seniority
Lead
Job Description
Staff Engineer, Supplier Quality Engineering
Stryker
• Act as a key liaison between suppliers and Stryker • Drive continuous improvement across the global supply base • Lead supplier-related CAPA review and management • Perform detailed process reviews and audits at supplier manufacturing sites • Track, analyze, and report supplier KPIs and performance metrics to leadership • Assess and improve supplier process control documentation and Quality Management Systems • Identify, prioritize, and execute supplier improvement and cost-reduction initiatives • Analyze nonconformance data to address systemic supplier quality issues • Support PMO initiatives and lead portfolios of supplier improvement projects • Collaborate cross-functionally to prioritize supplier change requests and improvement actions • Execute proactive supplier site visits and support third-party audits related to Supplier Quality CAPA • Transfer supplier “lessons learned” back to R&D to support next-generation design improvements • Train, mentor, and develop less experienced engineers while championing best-practice sharing across Stryker
Job Requirements
- Bachelor’s degree in engineering or related field
- Minimum 4 years of relevant experience in Supplier Quality or related quality engineering roles
- Experience working on Internal/External Quality Audits
- Experience working in a highly regulated environment
- Working knowledge of FMEA, validation programs, and SPC
- Foundational understanding of manufacturing drawings and tolerancing
- Basic statistical analysis skills
- Strong problem-solving and root cause analysis capability
- Ability to communicate effectively with suppliers and internal stakeholders
- Proven ability to manage multiple priorities and projects
- Willingness to travel 30% domestically
- Preferred External Quality Auditor qualification (ISO 13485, 21 CFR 820, or equivalent)
- Experience supporting API or pharmaceutical manufacturing environments
- Experience working with global suppliers or global strategic partners
- Advanced problem-solving or continuous improvement expertise (e.g., Six Sigma).
Benefits
- Annual salary plus bonus eligible
- Benefits available
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