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Principal Process Engineer

Medtronic
Northridge, United Statesfull_timeVerifiedPosted 7 Nov 2025
💰 $188,400/yr

About the role

We anticipate the application window for this opening will close on - 14 Nov 2025


 

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

This position will play a key role in the development of various new/improved chemistry layers/coatings of glucose sensors by designing and executing design feasibility, process development, and manufacturing transfer. This role will be responsible for driving the product build documentation, design and executing experiments and builds of sensors for pilot scale evaluations, execute data trending & statistical analysis. Upon successful process and design optimization, this role will subsequently support tech transfer to new product introduction and manufacturing teams. You will manage deliverables for multiple projects and maintain an effective system for tracking progress. You will be interfacing with Managers, Engineers &Technicians in R&D and New Product Introduction (NPI) Operations teams as well as Quality and Clinical groups to accomplish day to day activities. The candidate must have strong organizational skills, attention to details, an analytical mindset and ability to communicate effectively with multiple stakeholders.

This position is an exciting opportunity to work with Medtronic's Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our team with a bold opportunity to unleash our potential, enabling us to operate with greater speed and agility. As a separate entity, we anticipate leveraging increased investments to drive meaningful innovation and enhance our impact on patient care.

Responsibilities may include the following and other duties may be assigned.

  • Develop & utilize technical & wet lab skills associated with medical device coatings/deposition & relevant fabrication processes

  • Utilize design of experiments (DOEs), statistical process control, and statistical data analysis methodologies in developing new designs and processes to integrate with next generation sensors

  • Generate documentation following good documentation practices in relation to product builds & instructions, clinical documentation, specifications, etc. and drive approvals

  • Act as a key interface with Manufacturing/Production teams

  • Coordinate with material inventory and external or internal vendors in sourcing raw materials and parts for the prototype builds

  • Develop and support Bill Of Materials (BOM)

  • Oversee & coordinate device build, sterilization, and testing

  • Resolve non-compliance issues and inefficiency issues, recommending and implementing process changes.

  • Provides technical support to device failure analysis on devices

  • Attend prototype product build coordination meetings, including schedule management; gather and verify requirements and communicate updates to stakeholders in a timely manner

  • Utilize knowledge of project management, schedules and deliver on day-to-day tasks to accomplish goals for a specific project

Required Knowledge and Experience: Requires a Baccalaureate degree and minimum of 7 years of relevant experience OR Master's degree with a minimum of 5 years relevant experience OR PhD with 3 years relevant experience.

Nice to Haves:

  • Prior experience with coatings/deposition methodologies including spray, slot, spin, CVD, PVD, as relevant to medical device or semiconductor industries (ex: MEMS photolithography processes)

  • Standard wet lab techniques as applicable to chemistry or biology labs

  • Prior experience working in a manufacturing or prototype line in a cleanroom environment in medical device, pharmaceutical or semiconductor industry

  • Experience with statistical data analysis software (Ex. Minitab, JMP, etc.) and standard statistical tests (T-test, ANOVA)

  • Experience in programming with MATLAB and/or Python

  • Performed R&R studies, demonstrating process capability (Ppk & Cpk), and Qualification procedures (IQ/OQ/PQ)

  • Exposure to Design for Reliability and Manufacturability (DRM) principles and/or process and performance improvement tools such as Lean and/or Six Sigma

  • Experience with technical documentation (Work Instructions, laboratory notebooks, publications, engineering reports, change r

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Company

Medtronic

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