Supplier Quality Engineer

The Supplier Quality Engineer is responsible for ensuring that suppliers consistently deliver high-quality materials, components, and services that meet Healthcare's quality standards, regulatory requirements, and organizational procedures within the medical device industry. This role involves supplier qualification and onboarding, risk assessment, supplier audits, PPAP reviews, process validation, and continuous improvement initiatives. The position works closely with cross-functional and global teams to maintain supplier compliance, mitigate quality risks, and support product quality and reliability throughout the supply chain.

• Bachelor's degree in engineering, technical discipline, or a scientific field.
• Minimum of 8 years of experience in Supplier Quality Engineering or a related quality role within the medical device industry.
• Strong knowledge of medical device quality management systems, regulatory requirements, and supplier quality processes.
• Hands-on experience with supplier qualification, supplier audits, risk assessments, and Approved Supplier List (ASL) management
• Ensure suppliers consistently deliver materials, components, and services that meet Healthcare's quality and regulatory requirements.
• Evaluate, qualify, and onboard new suppliers into the Approved Supplier List (ASL).
• Conduct product- and feature-level quality impact assessments and maintain supporting documentation.
• Review and approve Production Part Approval Process (PPAP) documentation, including Control Plans, Process Flow Charts, Process Drawings, Capability Studies, Design Failure Mode and Effects Analysis (DFMEA), and Process Failure Mode and Effects Analysis (PFMEA).
• Perform supplier risk segmentation, maintain supplier risk profiles, and implement appropriate risk mitigation strategies.
• Facilitate Supplier Quality Agreements and conduct supplier quality audits to ensure compliance with applicable quality system and regulatory requirements.
• Coordinate supplier evaluation and selection activities for new suppliers and changes to existing products, components, or manufacturing processes.
• Support and approve process validation activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
• Review and support Measurement System Analysis (MSA), Test Method Validation (TMV), and Control Plan development and implementation.
• Route quality documentation through Product Lifecycle Management (PLM) systems, track approval workflows, and ensure timely document release.
• Collaborate with Global Supplier Quality teams to implement Supplier Data Review (SDR) and Supplier Owned Quality (SOQ) initiatives.
• Partner with cross-functional teams to resolve supplier quality issues, drive corrective and preventive actions, and support continuous improvement.
• Maintain accurate supplier quality records and ensure compliance with applicable medical device quality standards, regulatory requirements, and internal procedures.