SQE II_CMSQ

Technical Specialist Career Stream at Medtronic focusing on supplier quality, GMP compliance, and quality engineering across the product lifecycle. Responsibilities include qualifying suppliers, administering supplier programs, overseeing receiving inspection, auditing designated suppliers for GMP and quality standards, developing and prioritizing audit schedules, evaluating supplier internal functions, supporting Pre-Market Quality for New Product Development, providing technical guidance on quality compliance throughout the NPD lifecycle, and collaborating with Component Engineers to implement Product Acceptance Sampling Strategy, Approved Supplier List coordination, and Control Plans for new products. Emphasis on delivering R&D/system initiatives, mentoring, and cross-functional collaboration to drive high-quality, reliable medical devices.