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Remote Medical Device Project Manager Jobs (NOW HIRING)

Experience with medical device capital equipment development required and * 10+ years of experience ... For fully remote positions, compensation will comply with all applicable federal, state, and local ...

... Medical Device space * Experience with GxP guidelines, Software Development Life Cycle (SDLC ... Remote and Hybrid Work * Time Off When You Need It * Benefits That Flex * Professional Development ...

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... preferably medical device) * Confident presence and strong influencing skills; excellent ... Demonstrated proficiency in managing complex sales cycles typically defined as six months or longer ...

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... preferably medical device) * Confident presence and strong influencing skills; excellent ... Demonstrated proficiency in managing complex sales cycles typically defined as six months or longer ...

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Remote Medical Device Project Manager information

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$38.5K

$102.7K

$162K

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

As of Jun 7, 2026, the average yearly pay for remote medical device project manager in the United States is $102,682.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,500.00 and $123,000.00 per year, depending on experience, location, and employer.

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

To thrive as a Remote Medical Device Project Manager, you need strong project management skills, a background in engineering or life sciences, and knowledge of medical device regulations, often supported by a PMP certification or similar credential. Familiarity with project management tools like Microsoft Project, collaboration platforms, and regulatory submission systems (such as FDA eCTD) is commonly required. Exceptional communication, leadership, and problem-solving abilities help in leading cross-functional remote teams and managing stakeholders. These skills are crucial for ensuring regulatory compliance, timely product development, and effective coordination in a dispersed work environment.

What are some common challenges faced by Remote Medical Device Project Managers, and how can they be addressed?

Remote Medical Device Project Managers often face challenges such as coordinating cross-functional teams across different time zones, maintaining clear communication with stakeholders, and ensuring regulatory compliance from a distance. These challenges can be addressed by establishing regular virtual meetings, using project management tools to track progress, and implementing standardized documentation practices. Building strong relationships with team members and fostering an open communication culture are also key to overcoming these hurdles and ensuring project success.

What does a Remote Medical Device Project Manager do?

A Remote Medical Device Project Manager oversees the planning, execution, and completion of projects related to medical devices, all while working remotely. They coordinate cross-functional teams, manage timelines and budgets, ensure regulatory compliance, and communicate with stakeholders to keep projects on track. Their role is crucial for ensuring that new medical devices are developed efficiently and safely, meeting both company goals and industry standards.

What is the difference between Remote Medical Device Project Manager vs Remote Medical Device Quality Assurance Specialist?

AspectRemote Medical Device Project ManagerRemote Medical Device Quality Assurance Specialist
CertificationsPMP, CAPM, or equivalent project management certificationsISO 13485 Lead Auditor, CQE, or similar quality assurance certifications
Work EnvironmentOversees project timelines, teams, and deliverables remotely within medical device companiesEnsures compliance, audits, and quality processes remotely in medical device manufacturing or development
Employer & Industry UsageUsed by medical device firms managing product development projects remotelyCommon in companies focusing on quality standards and regulatory compliance remotely

The Remote Medical Device Project Manager focuses on managing project timelines, teams, and deliverables remotely, ensuring successful product development. In contrast, the Remote Medical Device Quality Assurance Specialist concentrates on maintaining quality standards, conducting audits, and ensuring regulatory compliance remotely. Both roles require specialized certifications and are vital in the medical device industry, often working in similar remote environments but with distinct responsibilities.

More about Remote Medical Device Project Manager jobs
What cities are hiring for Remote Medical Device Project Manager jobs? Cities with the most Remote Medical Device Project Manager job openings:
What states have the most Remote Medical Device Project Manager jobs? States with the most job openings for Remote Medical Device Project Manager jobs include:
Infographic showing various Remote Medical Device Project Manager job openings in the United States as of May 2026, with employment types broken down into 64% Full Time, 29% Part Time, and 7% Contract. Highlights an 100% Remote job distribution, with an average salary of $102,682 per year, or $49.4 per hour.
Medical Device Risk Management Advisor (Part-Time, Remote)

Medical Device Risk Management Advisor (Part-Time, Remote)

FocusKPI Inc.

Boston, MA โ€ข Remote

Contractor

Posted 19 days ago


Job description

We are building an AI-powered platform to support medical device risk management and regulatory documentation (including ISO 14971 and design controls), and are looking for a few professionals to serve as ongoing product feedback advisors.

This is a flexible, part-time opportunity for experienced professionals who can periodically test new features, review workflows, and provide practical feedback based on real-world medical device and regulatory experience. Your input will directly shape how the product supports day-to-day work in regulated environments.

What Youโ€™ll Do
  • Test new features and prototypes periodically
  • Provide feedback on usability and regulatory alignment
  • Review risk management and documentation workflows
  • Suggest improvements based on real industry practice
  • Join occasional 30โ€“45 minute feedback sessions
Time Commitment
  • Flexible, ongoing engagement
  • Approximately 1โ€“2 hours per week or biweekly
  • Fully remote
Preferred Background
  • Medical device regulatory affairs or quality assurance
  • Experience with ISO 14971 risk management
  • Design controls / DHF documentation
  • 510(k), De Novo, or PMA experience is a plus
  • Risk management file, FMEA, or hazard analysis experience

Consultants and industry professionals are welcome.

How to Apply

If youโ€™re interested, please complete this short screening form so we can better understand your background:
https://forms.gle/jgj1ZN2jtAGGAbYQA

Weโ€™ll follow up with selected candidates to schedule an initial session and discuss next steps.

NOTICE: Please be aware of fraudulent emails regarding job postings, job offers and fake checks. FocusKPI's recruiting team will strictly reach out via @focuskpi.com email domain. If you have received fraudulent emails now or in the past, please report it to https://reportfraud.ftc.gov/ .
The domain @focuskpijobs.com is fraudulent and not related to FocusKPI. Please do not not reply or communicate to anyone with @focuskpijobs.com.

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FocusKPI logo

About FocusKPI

Sourced by ZipRecruiter

Industry

Computing infrastructure providers, data processing, web hosting

Company size

51 - 200 Employees

Headquarters location

Santa Clara, CA, US

Year founded

2010