Stryker

Together with our customers, we are driven to make healthcare better. #WeAreStryker

Staff Engineer, Supplier Quality Engineering

QA EngineerQA EngineerFull TimeRemoteTeam 10,001+Since 1941H1B SponsorCompany SiteLinkedIn

Location

Illinois

Posted

5 days ago

Salary

$98.2K - $163.7K / year

Bachelor Degree4 yrs expEnglish

Job Description

• 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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