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Medical Device Program Manager Jobs in Virginia (NOW HIRING)

Danaher

Sales Representative Medical Device

Richmond, VA · 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 ...

Caraballo Consulting & Associates L

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QA Manufacturing Engineer - Medical Device

Sterling, VA · On-site

$40 - $80/hr

... Medical Device company. The perfect candidate will perform the following activities: Key ... Complete the bulk download of documents and records from a Quality Management System. Required ...

Caraballo Consulting & Associates L

Be Seen First

QA Manufacturing Engineer - Medical Device

Sterling, VA · On-site

$40 - $80/hr

... Medical Device company. The perfect candidate will perform the following activities: Key ... Complete the bulk download of documents and records from a Quality Management System. Required ...

AeroVironment, Inc.

Program Manager

Herndon, VA · On-site

$170K - $230K/yr

Mobile Device and BYOD management in cloud computing environments. * Zero-Trust architecture ... AV offers an excellent benefits package including medical, dental vision, 401K with company ...

AeroVironment

Program Manager

Herndon, VA

$170K - $230K/yr

Mobile Device and BYOD management in cloud computing environments. * Zero-Trust architecture ... AV offers an excellent benefits package including medical, dental vision, 401K with company ...

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All JobsMedical Device Program JobsMedical Device Program Manager JobsMedical Device Program Manager Jobs in Virginia

Medical Device Program Manager information

See Virginia salary details

$38.2K

$106.5K

$155.7K

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

As of Aug 26, 2026, the average yearly pay for medical device program manager in Virginia is $106,539.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,800.00 and $131,400.00 per year, depending on experience, location, and employer.

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 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 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 popular job titles related to Medical Device Program Manager jobs in Virginia?

For Medical Device Program Manager jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Medical Device Program Manager jobs in Virginia look for?

The top searched job categories for Medical Device Program Manager jobs in Virginia are:

What cities in Virginia are hiring for Medical Device Program Manager jobs?

Cities in Virginia with the most Medical Device Program Manager job openings:

Medical Device Program Manager jobs near you
Infographic showing various Medical Device Program Manager job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 22% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $106,539 per year, or $51.2 per hour.

Medical Equipment Management Specialist

Falls Church, VA • On-site

KurzSolutions
Recruiting and Staffing Services • 11 - 50 employees
Learn more about KurzSolutionsexternal

Other

Re-posted 16 days ago

Job description

Medical Equipment Management Specialist

Medical Device Deployment in National Capital Region

DHA MHS Genesis Medical Device Integration

The Defense Health Agency's (DHA) National Capital Region Medical Directorate (Client MD) exercises authority, direction, and control over the Walter Reed National Military Medical Center, Fort Belvoir Community Hospital (FBCH), and their subordinate clinics; DiLorenzo TRICARE Health Clinic (DTHC), Tri-Service Dental Clinic, Fairfax Health Center, Dumfries Health Center, and the Joint Pathology Center (JPC). Effective October 1, 2019, the Client MD becomes the "Client Market Area." On this date the Client will assume direct control of additional healthcare operations at Andrews AFB, Fort Meade, Annapolis Naval Support Base, Quantico Marine Corps Base, and the Patuxent River Naval Air Station Client Market and tIMO Activities. The Medical Device Systems Security Program Management Office supports the Client's preparation and readiness to implement the MHS GENESIS electronic health record system in December 2022.

MHS GENESIS, the new DOD and VA electronic health record (EHR) requires a high level of medical device integration (MDI). Several critical medical equipment/device items and systems must integrate to the EHR to achieve optimal EHR utilization and effectiveness.

MDI is the electronic transmission of patient data from medical device to patient record. Medical equipment and systems that constitute this integration are therefore "devices" with respect to network infrastructure and security.

Medical devices that are integrated to the EHR must be MHS GENESIS compatible and cybercompliant in order to be declared "MHS GENESIS Ready." Only devices fulfilling this criteria can be authorized and approved for integration to the EHR. MHS GENESIS compatibility is confirmed by the DHA Medical Device Task Force. Cyber compliance is determined by Defense Health Agency officials who administer NIST cyber security guidelines and criteria within the Military Health System. The DHA Medical Device Task Force monitors device compliance and is therefore also a key source to verify cyber compliance.

DHA Medical Device Guidance (November 2017) prescribes MHS GENESIS readiness, Risk Management Framework (RMF)/cyber security compliance, and medical device standardization as operating requirements for DHA activities.

DHA's National Capital Region (Client) Director of Logistics and Acquisition established the Medical Device System Security (MDSS) Program Management Office (PMO) in October 2017 to achieve medical device readiness within the Client; specifically, Walter Reed National Military Medical Center (WRNMMC) and the Fort Belvoir Community Hospital (FBCH). On October 1, 2019 the Client Market Area officially adds medical activities at Andrews AFB, Fort Meade, Annapolis Naval Base, Patuxent River, and Quantico Marine Corps Base to its MHS GENESIS implementation program.

KurzSolutions is committed to improving Federal outcomes by providing Agencies with the top talent in the market.

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