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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Supplier Quality Management, ensuring compliance with medical device regulations and Good Manufacturing Practices. Proven ability to coordinate quality assurance activities, drive continuous improvement, and effectively communicate with cross-functional teams.
Highest-signal resume keywords
Supplier Quality ManagementGood Manufacturing PracticesQuality Systems ExperienceRegulatory ComplianceContinuous Improvement
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Quality EngineeringSupplier AuditsNonconforming Product ManagementMaterial Review Board CoordinationSupplier Performance Evaluation
Soft Skills
CommunicationCollaborationProblem-Solving
Industry Keywords
Medical Device IndustryManufacturing QualitySupplier Quality ActivitiesRegulated Manufacturing
About the role
Key responsibilities & impact- Manage supplier quality issues across assigned external manufacturers, ensuring material quality concerns are documented, communicated, investigated, and addressed
- Coordinate Material Review Board activities with business units to support timely assessment and disposition of potentially nonconforming products
- Serve as the Supplier Quality point of contact during internal and external audits and coordinate required follow-up activities
- Ensure supplier compliance with applicable medical device regulations, Good Manufacturing Practices, and Stryker quality requirements
- Partner with Manufacturing, Quality, Procurement, Strategic Sourcing, and business units to assess and resolve supplier and material quality issues
- Track supplier quality key performance indicators, report metrics during monthly business reviews, and participate in supplier performance evaluations
- Oversee supplier quality documentation and the Approved Supplier List in partnership with Procurement
- Drive continuous improvement activities with external manufacturing partners and provide technical guidance related to supplier quality systems and regulatory requirements
Requirements
What you’ll need- Bachelor’s degree in Engineering or a related technical field
- Minimum 5 years of experience in Quality Engineering, Supplier Quality, Manufacturing Quality, or a related quality function
- Professional working proficiency in English
- Experience working with quality systems, supplier quality, manufacturing processes, or regulatory compliance
- Experience within the medical device or another regulated manufacturing industry
- Experience supporting external manufacturers, contract manufacturers, or supplier quality activities
- Experience with Good Manufacturing Practices, supplier audits, nonconforming product management, and continuous improvement
Benefits
Comp & perks- Hybrid work flexibility
- Travel opportunity/requirement of 20%