Supplier Qual Engineer II.
Medtronic INC · 🌍 Tijuana, Baja California, Mexico
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Sponsor Radar — Medtronic INC
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About the role
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life Supplier Quality Engineer II Responsibilities may include the following and other duties may be assigned. • Ensures that suppliers deliver quality parts, materials, and services. • Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness. • Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur. • Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met. • Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation. • Some individuals may have responsibilities that include Pre-Market Supplier Quality and duties may include: Provides Pre-Market Quality Engineering support to New Product Development (NPD) working in partnership with the Component Engineering and Post-Market Supplier Quality Teams, to deliver quality parts, materials, and services, prevent defects, and allow Medtronic to provide customers with the highest quality and reliable products. • Provides technical guidance and quality compliance for Supplier Quality engagement throughout the NPD lifecycle on newly qualified parts from NPD and implementing strategies for driving product quality and continuous improvement, ensuring purchased products and components are manufactured and qualified in accordance to applicable industry standards, regulatory requirements, and customer requirements. • Collaborates with Component Engineers to develop and deliver the Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and Control Plans for new products. • Define Receiving Inspection requirements as required and associated test method validation for all internal Medtronic Test Methods. Nice to Have (Preferred Qualifications) • Bachelor’s degree in Engineering, Science, or technical field with 3+ years’ experience in Medical Device OR Advanced degree in Engineering, Science or technical field with 1+ years of experience in Engineering or Quality. • 2+ years of supplier quality experience in the medical device industry or related field with supplier quality management experience • Experience supporting manufacturing processes including printed circuit board assembly, manual assembly, machining, molding (dip/injection), etc. • Demonstrated working knowledge of supplier controls, process validation, failure investigation techniques, nonconforming product controls, and protocol/report generation • Project Management experience • First Time Quality (FTQ) Coach or Six Sigma / DFSS / Lean Green Belt • Quality System Lead Auditor experience (ISO 13485) • Working knowledge of Statistical Tools (Design of Experiments, Measurement System Analysis, Process Capability and Statistical Process Control) • Strong Oral and Written communication skills (English and Spanish) • Ability to work in a team/partnership environment TECHNICAL SPECIALIST CAREER STREAM: An individual contributor with responsibility in our technical functions to advance existing technology or introduce new