Senior Component Development Engineer (Supplier Quality)
LocationTempe, Arizona, United States of America
Work modeon-site
Typefull-time
SenioritySenior
DepartmentEngineering
Company size10,000+ people
First seenOct 4, 2026 · 1w ago
Verified live10h ago
At a glanceSummarised by Seekless from the posting.
Must have2
Bachelor’s degree in engineering, Science or technical field with 4+ years of work experience in Engineering and/or Quality OR Advanced degree with 2+ years OR PhD with 0 years
Experience in semiconductor manufacturing process, and/or electronics or chemical laboratory or clean room facilities
Nice to have6
Solid knowledge and experience on discrete components, timing components, and memory components
Preferred education: BSc/MSc in Electrical Engineering, Chemical Engineering, Material Science or related field
Familiarity with PLM systems, engineering processes (e.g. DFMEA, PPAP, TMV)
Professional certifications such as CQE, lead auditor, Six Sigma green/black belt, or PMP
Excellent communication and negotiation skills
Strong analytical, problem-solving, and cross-functional collaboration skills
Eligibility2
U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above; roles below Principal level require unrestricted U.S. work authorization at time of hire and for duration of employment
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required
Skills
PLM
DFMEA
PPAP
TMV
We anticipate the application window for this opening will close on - 18 Oct 2026
About the company
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
At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working onsite 5 days a week as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.
This is a rewarding opportunity in a highly talented and diverse team of engineers, technicians, and contractors located in Tempe, Arizona. Our campus is a technology development centers, where we help design, manufacture, and test circuit boards for all the CRM and Neuro implantable products, as well as wafers and services for products of other Operating Units like Diabetes.
Act boldly. Compete to win. Move with speed and decisiveness. Foster belonging. Deliver results…the right way. That’s the Medtronic Mindset — our cultural norms. Our brand is rooted in action, not just words. The Medtronic Mindset defines the expectations of our culture. Every person here plays a role in bringing it to life. We recognize your extraordinary potential to ensure future generations live better, healthier lives.
Responsibilities
Responsibilities may include the following and other duties may be assigned.
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Select, characterize, qualify, and release electronic components according to company standards.
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Create and release component specifications, datasheets, and drawings for new product introductions (NPI).
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Drive Quality rigor for New Product Development decisions, Capability & Reliability with Suppliers.
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Lead failure analysis, root cause investigation, and corrective actions for component-related issues while working with suppliers, manufacturing and quality teams to resolve technical and quality concerns.
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Work closely with program managers and cross functional teams including design, process, test, and reliability engineers to ensure project milestones are completed efficiently and on time.
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Monitor parts from acquisition through the manufacturing cycle and communicate and resolve supplier-related problems as they occur.
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Collaborate in qualification audits for new suppliers to ensure good manufacturing practices (GMP) and quality standards are met.
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Evaluate suppliers’ internal functions to assess their overall performance and provide feedback in assessment of their operation.
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Provide technical guidance and quality compliance for Supplier Quality engagement throughout the NPD lifecycle on newly qualified parts from NPD and implement 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.
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Evaluate alternate and second-source components to mitigate supply chain risks.
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Define Receiving Inspection requirements as required and associated test method validation for all internal Medtronic Test Methods.
Required Knowledge and Experience:
•
Bachelor’s degree in engineering, Science or technical field with 4+ years of work experience in Engineering and/or Quality OR Advanced degree in Engineering, Science or technical field with 2+ years of work experience in Engineering and/or Quality OR PhD with 0 years relevant experience.
•
Experience in semiconductor manufacturing process, and/or electronics or chemical laboratory or clean room facilities.
Nice to Have
•
Solid knowledge and experience on discrete components (e.g. capacitors and resistors), timing components (e.g. oscillators and RTC), and memory components (e.g. FRAM).
•
Preferred education: BSc/MSc in Electrical Engineering, Chemical Engineering, Material Science or related field.
•
Familiarity with PLM systems, engineering processes (e.g. DFMEA, PPAP, TMV).Professional certifications such as CQE, lead auditor, Six Sigma green/black belt, or PMP.
•
Excellent communication and negotiation skills (e.g. with suppliers for quality agreements, etc.)
•
Strong analytical, problem-solving, and cross-functional collaboration skills
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
Legal
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.