Engineering Program Manager
MedtronicAbout 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, we act boldly, compete to win, move with speed, foster belonging, and deliver results—the right way. This is the Medtronic Mindset, defining how we work and what we value. Our brand is rooted in action, and every team member plays a vital role in bringing our culture to life.We recognize your extraordinary potential to help ensure future generations live better, healthier lives. A career at Medtronic is purposeful, mission-driven, and unlike any other. We are committed to alleviating pain, restoring health, and extending life for millions worldwide.
You will be a part of a dedicated, experienced, and high-performing team at our Brooklyn Park site. At this facility, the assembler role is responsible for the day-to-day production and packaging of components used in our medical devices.
Onsite: 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 a minimum of 4 days a 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
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 products or software systems.
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 concepts from initial design to market release.
Manages feasibility studies of the design to determine if capable of functioning as intended.
Monitors documentation maintenance throughout all phases of research and development.
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.
Must Have: Minimum Requirements
To be considered for this role, please ensure the minimum requirements are evident in your applicant profile.
Practical experience leading and managing the execution of processes, projects, and initiatives within a defined functional area
Advanced knowledge and skills within a specific technical or professional discipline
Understanding of how work impacts other areas of the organization
Bachelor’s degree required (or, for degrees earned outside the United States, a degree that meets the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A))
Minimum of 5 years of relevant experience with a bachelor’s degree, or an advanced degree with a minimum of 3 years of relevant experience
Nice to Have
Experience in the medical device or other regulated industry (FDA, ISO 13485, design controls).
PMP, PgMP, or Agile certification (Scrum, SAFe).
Experience managing large, complex, or global engineering programs.
Apply for this role
Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.
Apply Now →Generate Application KitFree account required — sign up in 30s