ZipRecruiter

Log In

1

Medtech Project Manager Jobs in Minnesota (NOW HIRING)

Coloplast

Senior R&D CAD Specialist

Minneapolis, MN · On-site

$79K - $119K/yr

... MedTech Code of Conduct, and company policies. * Other duties as assigned Basic Qualifications * AA ... Knowledge of basic project management At Coloplast, we believe in recognizing and rewarding the ...

Comfort Medical

Senior R&D CAD Specialist

Minneapolis, MN · On-site

$79K - $119K/yr

... MedTech Code of Conduct, and company policies. * Other duties as assigned Basic Qualifications * AA ... Knowledge of basic project management At Coloplast, we believe in recognizing and rewarding the ...

LivaNova

Statistical Programmer II

Minneapolis, MN

$90K - $100K/yr

As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a ... Ability to manage priorities and timelines in a changing project environment. Desired ...

LivaNova

Regulatory & Clinical Specialist

Minneapolis, MN · Remote

$85K - $95K/yr

As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a ... projects. * Perform regulatory assessments of changes as part of the change management process.

LivaNova

Head of Sales, OSA

Minneapolis, MN

$325K - $430K/yr

As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a ... Ability to manage and prioritize multiple projects, and enjoy an agile, patient and quality focused ...

Coloplast

Senior Biostatistician

Minneapolis, MN · On-site

... MedTech Code of Conduct, and company policies. * Other duties as assigned Major Areas of ... Ability to manage multiple projects and priorities in a dynamic environment At Coloplast, we ...

Becton, Dickinson and Company

Support process improvement projects (templates, standard terms, system updates, etc.) to drive ... Weight management programs * Gastrointestinal health program * Substance use management program

Comfort Medical

Quality Engineer

Minneapolis, MN · On-site

$88K - $132K/yr

... MedTech Code of Conduct, and company policies. * Other duties as assigned Basic Qualifications ... Ability to effectively manage multiple projects and priorities. * Exercises judgment on details of ...

Comfort Medical

Senior Quality Engineer

Minneapolis, MN · On-site

$105K - $158K/yr

... MedTech Code of Conduct, and company policies. * Other duties as assigned Basic Qualifications ... Ability to effectively manage multiple projects and priorities. * Exercises judgment on details of ...

LivaNova

Senior UI Designer

Minneapolis, MN

$160K - $180K/yr

As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a ... Collaborate cross-functionally with product managers, engineering, human factors, regulatory, legal ...

previous page

Showing results 41-58

All JobsMedtech Project JobsMedtech Project Manager JobsMedtech Project Manager Jobs in Minnesota

Medtech Project Manager information

What does a Medtech Project Manager do?

A Medtech Project Manager oversees the planning, execution, and delivery of projects related to medical technology, such as the development of medical devices or healthcare software. They coordinate cross-functional teams, manage timelines and budgets, and ensure compliance with regulatory standards. Their role is crucial in bridging the gap between technical development, clinical requirements, and business goals to bring innovative medical solutions to market efficiently and safely.

What are the key skills and qualifications needed to thrive as a Medtech Project Manager, and why are they important?

To thrive as a Medtech Project Manager, you need a strong background in project management, biomedical engineering or life sciences, and a solid understanding of regulatory requirements, often supported by a relevant degree and PMP or similar certification. Familiarity with project management software like MS Project or Jira, as well as knowledge of FDA/CE regulations and quality management systems, is typically required. Exceptional leadership, communication, and problem-solving skills help drive cross-functional teams and manage stakeholder expectations. These abilities ensure timely product development, regulatory compliance, and successful project outcomes in the highly regulated Medtech industry.

How does a Medtech Project Manager typically collaborate with cross-functional teams during the product development lifecycle?

A Medtech Project Manager frequently works with cross-functional teams, including R&D, regulatory affairs, quality assurance, marketing, and manufacturing. They coordinate efforts by facilitating regular meetings, setting clear timelines, and ensuring all team members are aligned with project goals and compliance requirements. Strong communication skills are essential, as the Project Manager must translate technical updates between departments and resolve potential roadblocks promptly. This collaborative approach helps deliver innovative medical technologies efficiently while meeting regulatory standards.

What is the difference between Medtech Project Manager vs Medical Device Engineer?

AspectMedtech Project ManagerMedical Device Engineer
Required credentialsBachelor's in engineering, project management certification (PMP)Bachelor's or higher in biomedical, mechanical, or electrical engineering
Work environmentProject teams, cross-functional collaboration, client interactionsDesign, development, testing, and manufacturing of medical devices
Employer & industry usageMedical device companies, healthcare tech firmsMedical device manufacturing, R&D departments
Common search & comparison intentUnderstanding project management roles in medtechTechnical engineering roles in medical device development

The Medtech Project Manager focuses on overseeing medical device projects, coordinating teams, and ensuring timely delivery. In contrast, a Medical Device Engineer is primarily involved in designing, developing, and testing medical devices. Both roles require engineering backgrounds, but their daily tasks and responsibilities differ significantly, catering to different aspects of the medical device lifecycle.

What are popular job titles related to Medtech Project Manager jobs in Minnesota? For Medtech Project Manager jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Medtech Project Manager jobs in Minnesota look for? The top searched job categories for Medtech Project Manager jobs in Minnesota are:
What cities in Minnesota are hiring for Medtech Project Manager jobs? Cities in Minnesota with the most Medtech Project Manager job openings:
Medtech Project Manager jobs near you

Principal Design Assurance Engineer

Mobia Medical, Inc.

Fridley, MN • On-site

$110K - $160K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 11 days ago

Job description

About Mobia
Mobia Medical is a commercial-stage medtech companydelivering breakthrough stroke recovery solutions. The company's Vivistim® Paired VNS™ Therapy is thefirst and only FDA-approved implantable solution designedto improve function in chronic ischemic stroke survivorswith moderate to severe upper limb impairments. Vivistim® Paired VNS™ Therapy combines targeted vagusnerve stimulation with functional movement to promoteneuroplasticity and improve the brain's ability to relearnmotor skills. Mobia Medical is mobilizing patients, providers, and carepartners to establish a better way forward in stroke care.
About the role
The Principal Design Assurance Engineer supports product design and development activities and ensures the effective transfer of new products into manufacturing. This role partners closely with Regulatory, Operations, and Engineering teams to ensure compliance with applicable regulatory requirements and company standards.
The position is responsible for lifecycle management of assigned products, including maintenance of Design History Files (DHF) and Design Risk Management documentation.
This role applies hands-on electrical engineering expertise to support the design, analysis, verification, and sustaining of medical devices, including analog and digital circuits, power management, embedded systems, and electromechanical interfaces. The engineer interprets and evaluates electrical schematics, PCB layouts, component selection, and design tradeoffs to ensure alignment with design inputs, risk controls, and regulatory requirements.
The role serves as a technical bridge between Design Engineering and Quality by providing informed review and challenge of electrical design decisions.
In addition, this position supports nonconformance, CAPA, and complaint investigations and acts as a subject matter expert in hardware and electrical design controls, product and system risk management, robust design practices, test method development and validation, and technical investigations.
What you'll do
  • Provide Design Assurance leadership throughout the design and development of new hardware and electrical medical device products
  • Support post-market sustaining activities including failure analysis, design change development and implementation, supplier performance evaluation, certifications, complaint investigations, and nonconformance disposition
  • Lead root cause investigations, corrective action development, and verification of effectiveness
  • Lead and support compliant development, verification, validation, and transfer of new products and processes into manufacturing
  • Serve as a subject matter expert in hardware and electrical design controls, risk management, verification & validation, and DHF maintenance
  • Support new process development, test method development and validation, process characterization, and technical investigations
  • Lead and participate in design verification and validation activities with clear documentation
  • Ensure hardware and electrical designs meet regulatory and company standards for quality, safety, performance, and reliability
  • Apply sound engineering methodologies to resolve technical issues and drive improvements
  • Collaborate with Product Development, Sustaining Engineering, Quality, Regulatory, and Operations teams
  • Participate in design reviews and phase-gate reviews
  • Contribute to project planning, cost estimates, schedules, and performance requirements
  • Prepare and deliver technical presentations
  • Provide leadership and mentoring to engineers and project team members
  • Support audits and regulatory inspections
  • Provide backup support for other QA functions
  • Perform other duties as assigned

Qualifications
  • Bachelor's degree in Electrical, Biomedical, Mechanical Engineering, or related discipline with 10+ years of progressive experience, or equivalent combination of education and experience
  • Experience applying hardware and electrical design controls in regulated industries
  • Quality engineering experience or certification preferred
  • Strong knowledge of:
    • Medical device design controls
    • Risk management
    • New product development
    • DHF maintenance
    • Verification and validation testing
  • Experience with test method development and validation
  • Strong communication skills with ability to explain technical concepts clearly
  • Demonstrated ability to lead technical teams through collaboration and influence
  • In-depth knowledge of applicable regulations and standards, including:
    • FDA 21 CFR Part 820
    • ISO 13485
    • ISO 14971
    • IEC 60601
    • IEC 61010 (as applicable)
    • ISO 10993 (as applicable)
    • EU MDR
  • Strong analytical and problem-solving skills
  • Ability to work independently while exercising sound judgment
  • Proficiency with Microsoft Office and engineering/documentation tools
  • Strong organizational and time-management skills
  • Demonstrated success achieving quality and compliance objectives

Equal Opportunity Employer
Mobia Medical provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
Benefits
Mobia Medical provides a comprehensive benefits program to employees. It includes medical, dental and vision plans along with an FSA. Employees may participate in the company 401(k) plan with company matching. The company offers an unlimited Paid Time Off (PTO) program and approximately 18 paid company holidays per year.
Apply now
The pay range for this role is:
110,000 - 160,000 USD per year (US National)

Apply