Principal Process Engineer, Injection Molding - NMPH - Rice Creek/Fridley, MN (Onsite)

We anticipate the application window for this opening will close on - 31 Oct 2026

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

• Medtronic Neuroscience is transforming care for patients with neurological, spinal, chronic pain, bladder, and bowel conditions. Through meaningful innovation, advanced neuromodulation technologies, and strong clinical partnerships, we empower clinicians to deliver targeted therapies that restore function, relieve symptoms, improve quality of life, and help patients regain confidence, independence, and greater control over their health.
• Within Advanced Manufacturing Engineering, this role supports early-stage manufacturing development for next-generation implantable medical devices, partnering closely with research and development teams to evaluate manufacturability, establish scalable process concepts, and accelerate the transition from product concept to manufacturing readiness.

This position is based at the Rice Creek facility in Fridley, Minnesota and requires a minimum of four days onsite each week in a laboratory and engineering development environment. The role includes collaboration with internal product development teams, manufacturing sites, contract manufacturers, tooling suppliers, and external development partners. <25% travel may be required to support manufacturing partners and technology transfer activities.

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As Principal Process Engineer, Advanced Manufacturing Engineering (AME), you will provide technical leadership for manufacturing feasibility, rapid prototyping, and process development efforts supporting emerging implantable device technologies. This role focuses on developing and maturing manufacturing processes for complex implantable assemblies, identifying process risks, and establishing scalable manufacturing approaches that support future commercialization.

The position serves as a key manufacturing partner to research and development teams while influencing manufacturing strategy, technical standards, and organizational capability development.

Primary Responsibilities

Lead manufacturing feasibility assessments and process development activities for novel implantable medical device concepts and emerging therapies.

Develop and evaluate proof-of-concept manufacturing methods for implantable assemblies, stimulation leads, and miniature electromechanical components.

Drive rapid prototyping and iterative experimentation to assess manufacturability, process capability, failure mechanisms, and design tradeoffs.

Provide technical leadership in micro-insert molding, over-molding, precision injection molding, mold tool design, implantable lead assembly, and precision assembly technologies.

Partner with research and development teams to apply Design for Manufacturability (DFM) and Design for Assembly (DFA) principles during product development.

Establish process characterization strategies, design of experiments (DOE), process windows, and manufacturing readiness assessments to support process maturation.

Collaborate with manufacturing sites, contract manufacturers, tooling vendors, and automation suppliers to transition prototype processes into scalable production solutions.

Mentor engineers and influence technical decision-making across cross-functional teams to strengthen manufacturing capability and engineering rigor.

Required Qualifications

Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Biomedical Engineering, or related engineering discipline and a minimum of 7 years of experience in manufacturing engineering, OR

Master's degree in manufacturing engineering, process development, or medical device manufacturing and a minimum of 5 years of relevant experience, OR

PhD with minimum of 3 years of relevant experience

Demonstrated expertise in micro-insert molding and over-molding, including mold tool design, process development, and molding process optimization.

Experience developing, characterizing, and troubleshooting manufacturing processes for precision-engineered products or assemblies.

Experience designing and executing process characterization studies and Design of Experiments (DOE) to establish process capability and operating windows.

Preferred Qualifications

• Experience with implantable lead manufacturing, conductor assembly, or other implantable medical device manufacturing processes.
• Experience with precision assembly automation, fixture design, and advanced manufacturing technologies.
• Experience supporting early feasibility manufacturing, rapid prototyping, and iterative product development environments.
• Experience transferring manufacturing processes from development or pilot environments into commercial-scale production.
• Experience working with contract manufacturers, tooling suppliers, and external development partners to develop scalable manufacturing solutions.
• 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
• 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.
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Medtronic benefits and compensation plans

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