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Medical Device Program Manager Jobs in Excelsior, MN

Sr. Engineer, Medical Device R&D

Edina, MN · On-site

$108K - $148K/yr

This role will lead product design and development projects of new medical devices. REQUIREMENTS ... Strong Device Design Control and Risk Management * Biocompatibility research and testing experience ...

New

Assembly - Medical

Minnetonka, MN

$18.25 - $22.50/hr

  • Medical

  • Dental

  • Life

  • Retirement

This role is with a leading medical device manufacturing organization, is seeking Operators to join ... Comprehensive training and development programs Upon completion of waiting period associates are ...

... to focus solely on medical device materials for safety. NAMSA started testing medical devices ... Program/project management experience preferred PMP and CAPM certification preferred. Working ...

... to focus solely on medical device materials for safety. NAMSA started testing medical devices ... Program/project management experience preferred PMP and CAPM certification preferred. Working ...

Medical Assembly

Minneapolis, MN · On-site

$18 - $21/hr

  • Medical

  • Dental

  • Retirement

  • PTO

Jump into the world of medical device assembly. Become a part of something bigger with Medtronic ... Reward Programs Duties and Responsibilities * Assemble or inspect medical devices * Set up and ...

Medical Affairs Manager (Remote)

Minneapolis, MN · Remote

$190K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Medical Affairs Program Manager is responsible for supporting evidence strategies and for ... device industry in the US. Major Areas of Accountability * Partner with US and global cross ...

Showing results 41-60

Medical Device Program Manager information

See Excelsior, MN salary details

$43K

$120.1K

$175.5K

How much do medical device program manager jobs pay per year?

As of Aug 15, 2026, the average yearly pay for medical device program manager in Excelsior, MN is $120,145.00, according to ZipRecruiter salary data. Most workers in this role earn between $88,900.00 and $148,100.00 per year, depending on experience, location, and employer.

What is the difference between Medical Device Program Manager vs Medical Device Quality Engineer?

AspectMedical Device Program ManagerMedical Device Quality Engineer
CredentialsProject management certifications, engineering degreeQuality assurance certifications (e.g., CQE), engineering degree
Work EnvironmentCross-functional teams, project planning, product developmentQuality systems, compliance, testing, and validation
Employer & Industry UsageMedical device companies, manufacturing, R&DRegulatory agencies, manufacturing, quality departments
Search & Comparison IntentManaging projects, product launches, timelinesEnsuring quality, compliance, risk management

The Medical Device Program Manager focuses on overseeing product development projects, coordinating teams, and ensuring timely delivery. In contrast, the Medical Device Quality Engineer concentrates on maintaining quality standards, regulatory compliance, and testing processes. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.

What are the key skills and qualifications needed to thrive as a medical device program manager, and why are they important?

To thrive as a Medical Device Program Manager, you need a strong background in project management, regulatory compliance, and biomedical engineering or a related field, often supported by a relevant degree and industry experience. Familiarity with project management tools (such as MS Project), quality management systems (QMS), and certifications like PMP or Six Sigma are highly valued. Exceptional leadership, cross-functional communication, and problem-solving skills help drive successful product development and team coordination. These competencies ensure programs meet regulatory standards, stay on schedule, and deliver safe, effective medical devices to market.

What is a medical device program manager?

A Medical Device Program Manager oversees the planning, development, and execution of projects related to medical devices within a company. They coordinate cross-functional teams, manage timelines, ensure regulatory compliance, and serve as the main point of contact for stakeholders. Their role is crucial in bringing safe and effective medical devices from concept to market, ensuring that all aspects of the program meet quality and regulatory standards. Medical Device Program Managers often work closely with engineering, quality assurance, regulatory affairs, and marketing teams.

How does a medical device program manager typically collaborate with cross-functional teams during product development?

A Medical Device Program Manager works closely with cross-functional teams including engineering, regulatory affairs, quality assurance, manufacturing, and marketing throughout the product development lifecycle. They coordinate timelines, facilitate communication, and resolve conflicts to ensure project milestones are met while maintaining compliance with regulatory standards. Regular meetings and progress updates are essential, as the Program Manager acts as a central point of contact to align various team goals and address issues proactively. This collaborative approach helps streamline development and supports successful product launches.

What job categories do people searching Medical Device Program Manager jobs in Excelsior, MN look for?

The top searched job categories for Medical Device Program Manager jobs in Excelsior, MN are:

What cities near Excelsior, MN are hiring for Medical Device Program Manager jobs?

Cities near Excelsior, MN with the most Medical Device Program Manager job openings:

Infographic showing various Medical Device Program Manager job openings in Excelsior, MN as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $120,145 per year, or $57.8 per hour.

Senior Design Assurance Engineer - Medical Device (Onsite - Arbor Lakes, MN) Contract

Pharmavise

Maple Grove, MN • On-site

Full-time

Re-posted 6 days ago


Job description


Job Role: Senior Design Assurance Engineer - Medical Device (Onsite - Arbor Lakes, MN) Contract
Overview:
From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com and follow us on LinkedIn: https://www.linkedin.com/company/pharmavisecorp
Our F500 Medical Device client has an exciting opportunity for a Senior Design Assurance Engineer.
Job Summary:
The Sr Design Assurance Engineer provides focused quality engineering leadership on sustaining design assurance activities. Design assurance drives the ISO14971 risk management process and the Verification & Validation (V&V) process. This includes quality plans, risk management plans and reports, hazard analysis, product risk management workbook (user FMEA and design FMEA), sampling systems / procedures and statistical techniques, verification protocols/testing/reports, validation protocols/testing/reports. This role will be responsible for supporting risk document and post market record review during remediation activities as well as ensuring quality and compliance through post commercialization sustaining activities.
Requirements
Required Qualifications
  • Bachelor's degree in mechanical, electrical, biomedical engineering, or related discipline

  • 5+ years of related experience in design assurance, new product development, or related medical device or regulated industry experience

  • Understanding of electrical safety standards IEC 60601

  • Experience with reliability testing

  • Demonstrated use of Quality tools/methodologies

  • Strong written/verbal communication skills.

  • Risk documentation per ISO14971

Preferred Qualifications:
  • Experience with class III medical devices
  • BS in Electrical Engineering
  • Previous R&D experience
  • Strong knowledge of QSR and ISO standards
  • Medical device experience
  • ASQ certification