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Principal R&D Engineer, Brooklyn Center (North), MN
MedtronicBrooklyn Center, United Statesfull_timeVerifiedPosted 15 Aug 2025
💰 $188,400/yr
About the role
We anticipate the application window for this opening will close on - 20 Aug 2025
At Medtronic, we push the limits of what technology can do to make tomorrow better than yesterday and that makes it an exciting and rewarding place to work. We value what makes you unique. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.
The Process Engineer will lead the development of manufacturing processes for new components at the Medtronic Energy and Component Center (MECC) for the Cardiac Rhythm Management (CRM) business. MECC supports the design, development, and production of components used in implantable devices.
This position will work with other functions within the program team; but will have ownership for plans, reports, data collection, or other means necessary to gain the knowledge required to create and document the associated manufacturing procedures. You will also collaborate with design colleagues to ensure designs are capable of meeting performance and manufacturing targets. This position will support in data collection and review of regulatory submission-ready documentation for the FDA and other regulatory bodies.
Our Cardiac Rhythm Management Operating Unit offers devices and therapies that treat patients with abnormal heart rhythms and heart failure. It is comprised of four key businesses: Cardiac Pacing Therapies, Defibrillation Solutions, Cardiovascular Diagnostics & Services, and Patient Care Systems. Together, we will transform the lives of people with cardiac arrhythmias and heart failure.
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 are working onsite 4 days per 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 role will require less than 10% of travel to enhance collaboration and ensure successful completion of projects.
In general, the following responsibilities apply for the Principal Process Engineer. This includes, but is not limited to the following:
• Work with cross functional teams, including Design, Operations, Quality, Reliability and Tooling, to develop processes for manufacturing components in a regulated industry.
• Understand final product and assembly specifications so that processes are created to achieve the specification.
• Create specifications for manufacturing equipment. Interface with equipment supplier during equipment build.
• Plan and execute process characterization, OQ/PQ plans and reports and process release activities, including TMVs.
• Plan and execute FAT/SAT and IQ.
• Use statistical methods to resolve technical challenges and evaluate capability of manufacturing processes.
• Create or update pFMEAs for new or existing assembly processes.
• Develop fixtures, tools, and procedures for manufacturing processes.
• Leads the innovation, development and/or optimization of new manufacturing concepts, processes and procedures for transfer to manufacturing operations.
• This can include scouting and feasibility work, material selection, process and equipment selection, tooling / fixture and equipment installation and assessment of inputs, outputs and alignment to requirements.
• Develops manufacturing processes that are applicable to statistical process control and may develop those techniques including the measurement systems.
• Ensures processes and procedures are in compliance with regulations.
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
A Day in the Life
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.At Medtronic, we push the limits of what technology can do to make tomorrow better than yesterday and that makes it an exciting and rewarding place to work. We value what makes you unique. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.
The Process Engineer will lead the development of manufacturing processes for new components at the Medtronic Energy and Component Center (MECC) for the Cardiac Rhythm Management (CRM) business. MECC supports the design, development, and production of components used in implantable devices.
This position will work with other functions within the program team; but will have ownership for plans, reports, data collection, or other means necessary to gain the knowledge required to create and document the associated manufacturing procedures. You will also collaborate with design colleagues to ensure designs are capable of meeting performance and manufacturing targets. This position will support in data collection and review of regulatory submission-ready documentation for the FDA and other regulatory bodies.
Our Cardiac Rhythm Management Operating Unit offers devices and therapies that treat patients with abnormal heart rhythms and heart failure. It is comprised of four key businesses: Cardiac Pacing Therapies, Defibrillation Solutions, Cardiovascular Diagnostics & Services, and Patient Care Systems. Together, we will transform the lives of people with cardiac arrhythmias and heart failure.
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 are working onsite 4 days per 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 role will require less than 10% of travel to enhance collaboration and ensure successful completion of projects.
In general, the following responsibilities apply for the Principal Process Engineer. This includes, but is not limited to the following:
• Work with cross functional teams, including Design, Operations, Quality, Reliability and Tooling, to develop processes for manufacturing components in a regulated industry.
• Understand final product and assembly specifications so that processes are created to achieve the specification.
• Create specifications for manufacturing equipment. Interface with equipment supplier during equipment build.
• Plan and execute process characterization, OQ/PQ plans and reports and process release activities, including TMVs.
• Plan and execute FAT/SAT and IQ.
• Use statistical methods to resolve technical challenges and evaluate capability of manufacturing processes.
• Create or update pFMEAs for new or existing assembly processes.
• Develop fixtures, tools, and procedures for manufacturing processes.
• Leads the innovation, development and/or optimization of new manufacturing concepts, processes and procedures for transfer to manufacturing operations.
• This can include scouting and feasibility work, material selection, process and equipment selection, tooling / fixture and equipment installation and assessment of inputs, outputs and alignment to requirements.
• Develops manufacturing processes that are applicable to statistical process control and may develop those techniques including the measurement systems.
• Ensures processes and procedures are in compliance with regulations.
Must Have: Minimum Requirements: To be considered for this role, please ensure the minimum requirements are evident on your resume.
- Bachelor’s degree in engineering or scientific field
- Minimum 7 years of relevant experience, or advanced degree with a minimum of 5 years of relevant experience.
Nice to Have (Desired & Preferred Qualifications):
- Experience in medical device manufacturing or manufacturing in highly regulated industry/environment
- Prior knowledge and experience in new product development
- Experience in batteries manufacturing and processes
- Working knowledge of statistical tools such as
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