Supplier Quality Engineer II

Supplier Quality Engineer (SQE) II

The Supplier Quality Engineer (SQE) II is responsible for executing supplier quality activities and supporting the quality performance of external product and service suppliers used in spinal orthopedic implants, instruments, software, and capital equipment. This role focuses on developing and maintaining supplier capability through audits, corrective actions, change management, and continuous improvement initiatives. The SQE II works cross-functionally with Supply Chain, R&D, Regulatory, Quality, and Operations to support new product development and sustaining activities.

Essential Duties and Responsibilities

• Supplier Quality Management
• Manage supplier quality activities, including performance monitoring, issue resolution, and continuous improvement initiatives
• Build and maintain effective working relationships with assigned suppliers, serving as a quality point of contact and supporting on-site supplier visits, audits, and periodic business or quality reviews.
• Support supplier selection, approval, classification, and development through a combination of audits and product or process qualifications.
• Conduct on-site audits and supplier performance evaluations based on company procedures and ensures compliance with the supplier's management system.
• Provides input into supplier audit schedules and ensure completion of audits per audit schedule.
• Utilize risk management methodologies to influence risk-based decisions tied to supplier qualification, supplier change requests, and nonconforming product.
• Support maintenance of the Approved Supplier List.
• Product Support
• Represent supplier quality engineering in technical teams, setting priorities for corrective action efforts and leading related failure investigations as required.
• Manage supplier change requests, ensuring cross-functional review, risk assessment, and compliance with internal change control and regulatory requirements.
• Support second sourcing initiatives by assisting with supplier qualification activities, risk assessments, and documentation to ensure alternate suppliers meet quality and regulatory requirements.
• Provide statistical support to suppliers allowing both to analyze manufacturing processes and to recommend appropriate process controls for ensuring product conformance to specification.
• Coordinate Manufacturer Qualification activities including but not limited to Part Qualifications, Gage R&R, correlation studies and process development.
• Perform customer complaint investigations on products manufactured by suppliers.
• Audits & Compliance
• Analyze supplier quality data and provide results for Management Review
• Supports SCAR process from beginning to end, implementing and follow-up of corrective and preventive actions.
• Participate in FDA, MDSAP, ISO and other regulatory audits.
• Traveling is approximately 10-30% as required.
• Other duties as assigned.