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Biomedical Product Manager Jobs (NOW HIRING)

Knowtex

Founding Technical Product Manager

San Francisco, CA · On-site

$196K - $227K/yr

Founding Technical Product Manager Knowtex • In-Person/Hybrid (San Francisco) About Knowtex ... Background in health informatics, biomedical data, or life sciences technology * Experience ...

Teleflex

Global Product Manager

Morrisville, NC · On-site

... biomedical engineering, business administration or other similar degree area. • At least 3 years experience in product management or project management. • Comfort level in medical environment ...

Teleflex

Global Product Manager

Morrisville, NC

... biomedical engineering, business administration or other similar degree area. At least 3 years ... in product management or project management. Comfort level in medical environment, with ...

Zifo

Product Manager - Benchling

Cambridge, MA · On-site

Benchling Product Manager **This role will require regular, on-site presence at our client site in ... We look for Science - Biotechnology, Pharmaceutical Technology, Biomedical Engineering ...

Zifo

Product Manager - Benchling

Cambridge, MA · On-site

Benchling Product Manager **This role will require regular, on-site presence at our client site in ... We look for Science - Biotechnology, Pharmaceutical Technology, Biomedical Engineering ...

Zifo

Product Manager - Benchling

Norwood, MA · On-site

Benchling Product Manager **This role will require regular, on-site presence at our client site in ... We look for Science - Biotechnology, Pharmaceutical Technology, Biomedical Engineering ...

Zifo

Product Manager - Benchling

Cambridge, MA · On-site

Benchling Product Manager **This role will require regular, on-site presence at our client site in ... We look for Science - Biotechnology, Pharmaceutical Technology, Biomedical Engineering ...

Zifo

Product Manager - Benchling

Norwood, MA · On-site

Benchling Product Manager **This role will require regular, on-site presence at our client site in ... We look for Science - Biotechnology, Pharmaceutical Technology, Biomedical Engineering ...

Genentech

Senior Principal Product Manager

Boston, MA · On-site

Responsibilities : • You lead the product development lifecycle from initial concept and strategy ... in biomedical settings • Proven ability to manage complexity and risk in early-phase or ...

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All JobsBiomedical Product Manager Jobs

Biomedical Product Manager information

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$51.5K

$159.4K

$197K

How much do biomedical product manager jobs pay per year?

As of Jun 15, 2026, the average yearly pay for biomedical product manager in the United States is $159,405.00, according to ZipRecruiter salary data. Most workers in this role earn between $141,000.00 and $197,000.00 per year, depending on experience, location, and employer.

What does a Biomedical Product Manager do?

A Biomedical Product Manager oversees the development, marketing, and lifecycle management of biomedical products such as medical devices or diagnostic equipment. They act as a bridge between engineering, regulatory, marketing, and sales teams to ensure products meet market needs and comply with industry regulations. Their responsibilities include market research, product strategy, and communicating product value to internal and external stakeholders. Ultimately, they play a key role in bringing innovative biomedical solutions to market.

What are some common challenges faced by Biomedical Product Managers when bringing new medical devices to market?

Biomedical Product Managers often face the challenge of navigating complex regulatory requirements, such as FDA approval, which can be time-consuming and require meticulous documentation. They must also coordinate closely with cross-functional teams—including R&D, quality assurance, and marketing—to ensure products meet both clinical needs and business objectives. Balancing innovation with compliance, managing project timelines, and adapting to rapidly changing technologies are all typical hurdles. Effective communication and a strong understanding of both technical and market demands are essential for success in this role.

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

To thrive as a Biomedical Product Manager, you need a solid background in biomedical engineering or life sciences, combined with experience in product development and project management. Familiarity with regulatory requirements (such as FDA or CE Mark), product lifecycle management software, and quality management systems is typically required. Outstanding communication, leadership, and problem-solving skills help you collaborate effectively across cross-functional teams and drive product success. These competencies are crucial for ensuring biomedical products meet market needs, comply with regulations, and achieve commercial goals.
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Biomedical Product Manager jobs near you
Infographic showing various Biomedical Product Manager job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 67% In-person, and 33% Hybrid job distribution, with an average salary of $159,405 per year, or $76.6 per hour.

Biomedical Engineer

Tunnell Government Services

Bethesda, MD

Other

Posted 18 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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