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Biomedical Engineer Manager Jobs in Reston, VA (NOW HIRING)

Blue Water Thinking

Biomedical Engineer

Washington, DC · On-site

The role requires strong project management skills, an in depth understanding of healthcare technology management (HTM), and experience working within the VA enterprise. The Biomedical Engineer will ...

Guidehouse

Biomedical Engineer

Rockville, MD

$65K - $108K/yr

We are currently searching for Biomedical Engineer to help maintain, perform repairs, and ... Able to successfully manage several high-priority tasks at the same time. The annual salary range ...

Guidehouse

Biomedical Engineer

Rockville, MD · On-site

$65K - $108K/yr

We are currently searching for Biomedical Engineer to help maintain, perform repairs, and ... Able to successfully manage several high-priority tasks at the same time. The annual salary range ...

Castalia Systems

Biomedical Engineer Senior

Reston, VA · On-site

$110.40K - $151.70K/yr

Castalia Systems is seeking a Biomedical Engineer, Senior to support to the government's all source ... Must be able to demonstrate in-depth analysis of analytic operations and knowledge management ...

Castalia Systems

Biomedical Engineer Senior

Reston, VA

$108.70K - $149.30K/yr

Castalia Systems is seeking a Biomedical Engineer, Senior to support to the government's all source ... Must be able to demonstrate in-depth analysis of analytic operations and knowledge management ...

Castalia Systems

Biomedical Engineer Senior

Reston, VA

$108.70K - $149.30K/yr

Job Summary: Castalia Systems is seeking a Biomedical Engineer, Senior to support to the ... Must be able to demonstrate in-depth analysis of analytic operations and knowledge management ...

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$42.7K

$98.6K

$145.7K

How much do biomedical engineer manager jobs pay per year?

As of Jun 1, 2026, the average yearly pay for biomedical engineer manager in Reston, VA is $98,633.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,500.00 and $120,700.00 per year, depending on experience, location, and employer.

What does a Biomedical Engineer Manager do?

A Biomedical Engineer Manager oversees the design, development, and maintenance of medical equipment and healthcare technology. They lead teams of biomedical engineers, ensuring compliance with industry regulations and safety standards. Their responsibilities include project management, budgeting, vendor coordination, and collaboration with healthcare professionals to improve medical device performance. Additionally, they may conduct research to innovate new technologies and optimize existing systems. Effective communication and leadership skills are essential for managing both technical and organizational aspects of the role.

What are the key skills and qualifications needed to thrive in the Biomedical Engineer Manager position, and why are they important?

To thrive as a Biomedical Engineer Manager, you need a strong background in biomedical engineering, project management experience, and often a relevant bachelor's or master's degree. Familiarity with regulatory compliance systems (such as FDA standards), medical device development tools, and quality assurance certifications like PMP or Six Sigma is highly valued. Outstanding interpersonal communication, leadership, and problem-solving skills help distinguish top performers in this role. These skills ensure successful project delivery, regulatory compliance, and effective team leadership in a complex, multidisciplinary environment.

What are the typical daily responsibilities of a Biomedical Engineer Manager?

A Biomedical Engineer Manager’s day often involves overseeing engineering teams, guiding medical device development projects, and ensuring product compliance with healthcare regulations. They regularly coordinate with cross-functional groups, including research scientists, clinicians, and regulatory specialists, to align project objectives and timelines. Managers also allocate resources, address technical and personnel challenges, and provide mentoring to junior engineers. This role requires balancing hands-on technical work with strategic planning to deliver safe, effective medical solutions on time and within budget.
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What cities near Reston, VA are hiring for Biomedical Engineer Manager jobs? Cities near Reston, VA with the most Biomedical Engineer Manager job openings:
Biomedical Engineer Manager jobs near you

Biomedical Engineer

Tunnell Government Services

Bethesda, MD

Other

Posted 3 days ago

Job description

Biomedical Engineer SME Position Description

The successful candidate will be a Biomedical Engineer, with broad experience in aspects of the discipline that are relevant to the medical device domain, e.g., design, development, refinement, etc. They will provide scientific, technical, product development, product validation, and sustaining engineering advice as part of regulatory review of medical devices, with specific attention to premarket submissions. Such submissions include Premarket Notification (510(k)), Premarket Approval Application (PMA), etc.

The candidate should  have demonstrated at the interface of advanced engineering and clinical medicine.  Expertise in areas of research and development, quality and regulatory affairs, manufacturing and production, and clinical evaluation and field support should be evident. Additional specialization in relevant areas, such as biomaterials, biomechanics, bioinstrumentation, is desired. 

The candidate should be familiar with applicable industry standards and regulatory requirements, such as, but not limited to, FDA Guidances (Appropriate Use of Voluntary Consensus Standards in Premarket Submissions for Medical Devices), US regulatory standards (21 CFR Part 820 -- Quality System Regulation), and ANSI standards (ANSI/AAMI/ISO 14971: Medical devices - Applications of risk management to medical devices).

Qualifications

  • The candidate must possess a bachelor's degree (BS) in biomedical engineering.
  • An advanced degree (MS, PhD) in a related/applicable field is strongly preferred.
  • 10 years of experience is required
  • Experience with directly supporting FDA 510(k) and related regulatory submissions is preferred
  • Exceptionally strong written and verbal communication skills
  • 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.)

Responsibilities

  • The primary focus of the role is to support analyses of medical devices relative to regulatory and technical aspects of biomedical engineering.
  • Provide consultation related to supporting medical device reviews (EUA, 510(k), PMA, IDE, Combination Devices, 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

Must be a US Citizen or Full Green Card holder.

Job Type:  Full Time Employee

Schedule:  Monday through Friday (No Holidays)

Location:  This position is 100% telework. 

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