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Medical Device Project Manager Jobs in Maple Grove, MN

Stereotaxis

Project Manager

Minneapolis, MN · On-site

Minimum 10 years' experience in the medical device industry 5+ years of project management experience in the medical device industry. Proven track record of managing complex, multi-disciplinary ...

Stereotaxis

Project Manager

Minneapolis, MN · On-site

... relevant medical device industry regulations and standards. • Identify potential project risks ... Hiring Manager Exemption Type # of Hires Needed 1 Wage Amount

Cirtec Medical

Sr. Project Manager

Brooklyn Park, MN · On-site

Position Summary: The Sr. Project Manager position is primarily responsible for managing and ... Lead and coordinate assigned medical device projects, including development activities and ...

Bracco

Medical Device Assembler I

Eden Prairie, MN · On-site

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Other duties or projects as required Qualifications (Knowledge, Skills & Abilities): Minimum * High ...

Bracco

Medical Device Assembler I

Eden Prairie, MN

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Other duties or projects as required Qualifications (Knowledge, Skills & Abilities): Minimum * High ...

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All JobsMedical Device Project JobsMedical Device Project Manager JobsMedical Device Project Manager Jobs in Maple Grove, MN

Medical Device Project Manager information

See Maple Grove, MN salary details

$39.4K

$105.1K

$165.9K

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

As of Aug 11, 2026, the average yearly pay for medical device project manager in Maple Grove, MN is $105,141.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,400.00 and $125,900.00 per year, depending on experience, location, and employer.

What are the day-to-day responsibilities of a medical device project manager?

As a Medical Device Project Manager, your daily duties typically include coordinating the activities of cross-functional teams—such as engineering, quality assurance, regulatory affairs, and marketing—to ensure project milestones are met. You'll oversee timelines, budgets, and documentation, while also addressing risks, facilitating communication, and managing stakeholder expectations. Regular tasks might involve leading project meetings, updating project trackers, monitoring regulatory compliance, and troubleshooting challenges that arise throughout the product development lifecycle. Successful project managers balance strategic planning with hands-on problem solving to keep complex medical device projects moving smoothly toward launch.

What is a medical device project manager?

A Medical Device Project Manager oversees the planning, development, and launch of medical devices, ensuring compliance with regulatory standards. They coordinate cross-functional teams, manage timelines, budgets, and risks, and facilitate communication between stakeholders. Their role involves working closely with engineering, regulatory, quality, and marketing teams to bring safe and effective medical devices to market.

What are the key skills and qualifications needed to thrive in a medical device project manager position, and why are they important?

To thrive as a Medical Device Project Manager, you need a strong knowledge of medical device development, regulatory compliance, and project management, often supported by a background in engineering or life sciences and certifications like PMP or Six Sigma. Familiarity with tools such as Microsoft Project, quality management systems (QMS), and regulatory submission platforms (such as FDA eSubmitter) is highly valuable. Excellent leadership, problem-solving skills, and effective communication are essential for coordinating cross-functional teams and navigating complex project demands. These skills are crucial for delivering compliant, high-quality medical devices on time and within budget while ensuring collaboration across technical and clinical stakeholders.

What job categories do people searching Medical Device Project Manager jobs in Maple Grove, MN look for? The top searched job categories for Medical Device Project Manager jobs in Maple Grove, MN are:
What cities near Maple Grove, MN are hiring for Medical Device Project Manager jobs? Cities near Maple Grove, MN with the most Medical Device Project Manager job openings:
Medical Device Project Manager jobs near you
Infographic showing various Medical Device Project Manager job openings in Maple Grove, MN as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $105,141 per year, or $50.5 per hour.

Senior Project Manager

Enterra Medical, Inc.

Saint Louis Park, MN • On-site

$150K - $165K/yr

Full-time

Re-posted 24 days ago

Job description

Senior Project Manager
Location: St. Louis Park, MN (Hybrid)
Job Summary:
We are seeking an experienced Senior Project Manager to lead product lifecycle and continuous improvement projects for active implantable medical devices (AIMDs). This role will be responsible for maintaining business continuity, improving existing designs, and managing product lifecycle changes. The ideal candidate will proactively lead cross-functional teams to identify, plan, and execute business critical projects.
Responsibilities:
  • Be the translator between business and technical to lead the identification of risks and opportunities and deliver solutions.
  • Drive planning and execution of R&D projects including design transfer, product upgrades, material obsolescence, cost-reduction initiatives, corrective actions, and geography expansions while ensuringproject milestones are met within scope, schedule, and budget.
  • Lead cross-functional teams including R&D, Quality, Regulatory, Operations, and Contract Design and Manufacturing Organizations.
  • Drive compliance with medical device standards and regulations, including ISO 13485, ISO 14971, IEC 62304, and IEC 60601.
  • Provide regular status updates and lead project reviews.
  • Ability to travel domestically and internationally up to 25%.

Required Qualifications:
  • Bachelor's degree in engineering or related field.
  • 7+ years of experience in project management and/or engineering for Class II/III medical devices.
  • Proven track record in medical device project management, including product launch through end of life.
  • Proven ability to influence both internal and external team members and leadership.
  • Strong knowledge of regulatory requirements for medical devices and experience with design controls, manufacturing process development, and risk management.

Preferred Qualifications:
  • MBA or master's degree in engineering or related field.
  • Experience with active implantable medical devices (e.g., neurostimulators, pacemakers, defibrillators, cochlear implants, or similar)
  • Proficient in current, best-practice project management methodologies and tools.
  • Previous participation in regulatory audits.
Total Compensation: $150,000-$165,000

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