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Engineering Supervisor

Medtronic
United Statesfull_timeVerifiedPosted 4 Jun 2026
💰 $152,400/yr($101,600/yr$152,400/yr)

About the role


 

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 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 work a minimum of five days per week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.

         

         

At Medtronic, Engineers are indispensable to achieving our Mission. That’s why we empower you to bring the best of your experience to bear on our market-leading portfolio of innovations. Apply your existing skills and develop new ones, with the training, mentorship, and guidance you need to continue to develop your expertise. With roles in specific business units, as well as at the corporate level, you’re sure to find an opportunity to make an impact that’s right for you.

The Manufacturing Engineering Manager is responsible for leading a team of technicians in the optimization of manufacturing equipment for the Crescent, Nautilus, BMLS, and Opus product lines. This role ensures that production operations consistently meet safety, quality, delivery, and cost objectives through equipment assembly, qualification, maintenance and repair. As an contributor, this role will work on projects and tasks to enhance and improve manufacturing processes and equipment while managing a team focused on maximizing uptime, insuring safety, and reducing cost.  Reporting into the Engineering Sr. Manager at Dexter, you will collaborate cross-functionally with inter-departmental teams of Engineers, Designers, Machinists and site teams such as  Quality, Regulatory, Operations, Released Product Engineering, and Supply Chain teams to maintain robust, reliable, and scalable manufacturing systems.

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

  • Plans, directs and implements all aspects of the company's design and development of new medical device producing equipment, fixtures and processes.
  • May develop, evaluate, implement and maintain technical quality assurance and control systems or reliability systems and standards pertaining to materials, techniques, or company products.
  • Oversees the investigation and evaluation of existing technologies.
  • Guides the conceptualization of new methodologies, materials, machines, processes or products.
  • Directs the development of new equipment or processes from initial concept through validation.
  • Manages feasibility studies of the design to determine if capable of functioning as intended.
  • Monitors documentation of preventative maintenance throughout all phases of equipment life.
  • Organizes the coordination of activities with outside suppliers and consultants to ensure timely delivery.
  • Selects, develops and evaluates personnel to ensure the efficient operation of the function.
  • Manages the team performance with measurable metrics, skill and professional growth opportunities, and career development.

Required Knowledge and Experience: 
Requires a Bachelor's degree and minimum of 1 year relevant experience.

Nice to Have:

·       Experience in medical manufacturing under FDA/GMP conditions in a manufacturing environment, preferably medical devices.

·       Experience as a Manufacturing Engineer.

·       Experience managing direct reports.

·       Excellent personal, organizational and leadership skills.

·       Proficiency with business software and network applications.

·       Knowledge of laws, regulations and standards governing medical device manufacturing.

·       Ability to lead DMAIC A3 problem solving processes.

·       Ability to interpret technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.

·       Ability to effectively present information to larg

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Company

Medtronic

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