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Medical Device Project Manager Jobs in Maryland (NOW HIRING)

Danaher

Sales Representative Medical Device

Baltimore, MD · On-site +1

$90K - $100K/yr

This position reports to the Regional Sales Manager and is part of the Blood Gas Sales Team and ... in a medical device industry preferred * 1+ years capital equipment sales experience preferred ...

Pinnaql

Automation Project Manager

Rockville, MD · On-site

$96K - $126K/yr

Experience supporting automation projects in pharmaceutical, biotech, medical device, or other GMP-regulated environments. * Strong project execution and stakeholder management skills. * Experience ...

Pinnaql

Automation Project Manager

Rockville, MD

$96K - $126K/yr

Experience supporting automation projects in pharmaceutical, biotech, medical device, or other GMP-regulated environments. * Strong project execution and stakeholder management skills. * Experience ...

Pinnaql

Automation Project Manager

Rockville, MD · On-site

$96K - $126K/yr

Experience supporting automation projects in pharmaceutical, biotech, medical device, or other GMP-regulated environments. * Strong project execution and stakeholder management skills. * Experience ...

Edwards Lifesciences Corporation

Proven successful project management and cross-functional leadership skills. * Ability to read and ... Ability to write routine MDR (Medical Device Reports)/MIR (Manufacturer Incident Report) and ...

CareMetx

Project Manager

Bethesda, MD · On-site

Project Manager POSITION SUMMARY : The Project Manager (PM) role within the Project Management ... Preferred experience in the pharmaceutical, medical device, biotech or healthcare hub services ...

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Medical Device Project Manager information

See Maryland salary details

$37.4K

$99.7K

$157.2K

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

As of Sep 7, 2026, the average yearly pay for medical device project manager in Maryland is $99,657.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,200.00 and $119,400.00 per year, depending on experience, location, and employer.

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 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 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 are popular job titles related to Medical Device Project Manager jobs in Maryland?

For Medical Device Project Manager jobs in Maryland, the most frequently searched job titles are:

What job categories do people searching Medical Device Project Manager jobs in Maryland look for?

The top searched job categories for Medical Device Project Manager jobs in Maryland are:

Medical Device Project Manager jobs near you
Infographic showing various Medical Device Project Manager job openings in Maryland as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 12% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $99,657 per year, or $47.9 per hour.

Combination Product (Medical Device) Reviewer

Tunnell Government Services

Bethesda, MD • On-site

Full-time

Posted 6 days ago

Job description

Tunnell Government Services, Inc., is comprised of the industry's leading scientists, medical and technical experts, and human capital and organizational development professionals. We approach all projects as a team and are committed to helping our clients transform and quickly achieve strategic goals. If you are interested in joining an employee-owned company that develops and implements innovative, integrated and differentiated solutions, please click on the links below to find the job that is right for you and contact us.
Combination Product (Medical Device) Reviewer
The mission of the FDA Center for Devices and Radiological Health (CDRH) is to protect and promote the public health. CDRH assures that patients and providers have timely and continued access to safe, effective, and high-quality medical devices and safe radiation-emitting products.
The Office of Clinical Evidence and Analysis within CDRH's Office of Product Evaluation and Quality (OPEQ) provides policy and program support regarding clinical trials, biostatistics, real-world evidence, epidemiological analysis and outreach and collaboration with hospitals and other external stakeholders.
Tunnell Government Services, Inc. is providing professional and scientific services to CDRH with expert consultants with scientific expertise in the regulation and approval and of medical devices. In general, these consultants provide consultation related to supporting medical device reviews (EUA, 510(k), PME and De Novo marketing applications, Pre-submissions); participate in meetings and teleconferences; coordinate meetings with internal and external stakeholders; develop written reviews and correspondence; write detailed documents and reports; and execute other administrative tasks related to CDRH's projects.
Tunnell is seeking a candidate to provide expert consulting services to assist the CDRH with their regulatory responsibilities, specific to the evaluation of pre-market submissions and lifecycle applications for medical products that combine medical devices with drugs and/or devices (e.g., drug-eluting stents, pre-filled syringes, inhalers).
This candidate should possess specific expertise and applicable training in regulatory scientific review, as relevant to:
  • Evaluating medical device investigations and clinical data to support regulatory decisions.
  • Ensuring clinical trial designs, biostatistics, and real-world evidence (RWE) comply with human subject protection standards and safety regulations before devices reach the market.

Key Duties and Responsibilities
  • Submission Evaluation: Review INDs, NDAs, BLAs, PMAs, and 510(k)s to assess how drug/biologic and device components interact.
  • Interdisciplinary Collaboration: Consult with cross-center experts (CDER, CDRH, CBER) and the Office of Combination Products to ensure aligned, consolidated regulatory feedback.
  • Design & Performance Review: Assess design controls, human factors (usability), and essential drug delivery outputs for complex combination therapies.
  • Guidance & Policy: Under direction of federal personnel, advise sponsors in pre-submission meetings and help develop or implement agency guidance documents.
  • Deficiency Identification: Draft formal deficiency letters for manufacturers if additional non-clinical, clinical, or manufacturing data is required.

Qualifications
  • The candidate must possess a bachelor's degree (BS) in a relevant field
  • An advanced degree (MD, MS, PhD) in a related/applicable field is strongly preferred.
  • 5-7 years of applicable experience is required, however advanced degrees can substitute for professional work experience
  • Candidates must demonstrate advanced professional experience in scientific, regulatory, or clinical research environments. Key background experiences include:
    • Trial Evaluation: Background evaluating clinical trial designs, bioequivalence data, and statistical protocols.
    • Regulatory Knowledge: Familiarity with the Federal Food, Drug, and Cosmetic (FD&C) Act, FDA guidance documents, and Good Clinical Practice (GCP) standards.
    • Industry Experience: Prior experience inside the medical device or pharmaceutical industry managing product lifecycles, clinical outcomes, or postmarket safety data.
  • Ability to communicate well with others using excellent written and verbal communication skills.
  • Excellent interpersonal skills, with the ability to effectively work both independently and within a team of technical personnel.
  • Proficiency with Microsoft Office Suite (Outlook, Word, Excel, etc.)

Job Type: Full Time
Schedule: Monday through Friday (No Holidays)
Location: This position is 100% telework.
Must be a US Citizen or Full Green Card holder.
Tunnell strives to hire and retain the most qualified talent. We believe that having employees with different backgrounds and capabilities contributes to the success of our business. To attract qualified applicants, Tunnell posts to a wide variety of job sites. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Please be advised that certain client contracts may outline specific requirements for onsite work. Tunnell employees and/or contractors are expected to comply with all client requirements, including any safety and health protocols.

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