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Medical Device Board Advisor Jobs (NOW HIRING)

Three Point Solutions

Medical Assembler

Menlo Park, CA · On-site

$20 - $22/hr

Medical Device Manufacturing Company Duration: 6 Months (Possible Extension) Location: Menlo Park ... Build modules, boards, panels, frames, and cables. * Follow diagrams, schematics, and work ...

Kyyba Inc

Medical Device Quality Technician

Irving, TX · On-site

$21 - $21.98/hr

... medical device assembly. o May operate more advanced measuring instruments as needed ... Perform visual and dimensional inspections of cable harness assemblies and printed circuit board ...

NexGoal

Medical Device Sales Representative

Phoenix, AZ · On-site

Build and maintain positive working relationships with medical and administrative support staff ... Board updates. NexGoal will not share your email address with any third parties. You will be free ...

Kyyba Inc

Medical Device Quality Technician

Irving, TX · On-site

$17.25 - $23.25/hr

... circuit board assemblies. • Maintain accurate inspection records, documentation, and filing ... medical device manufacturing or regulated environments. • Experience reviewing engineering ...

Three Point Solutions

Medical Assembler

Dexter, MI · On-site

$18 - $22/hr

Medical Device Manufacturing Company Duration : 12-Month Contract Assignment Location : Dexter, MI ... Assemble modules, boards, panels, frames, and cables. * Follow diagrams, schematics, and work ...

NAMSA

Medical Monitor, Medical Device CRO

$140K/yr

... device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug ... Advise on protocol amendments based on emerging safety data or regulatory feedback. Attend project ...

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Medical Device Board Advisor information

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$15

$53

$98

How much do medical device board advisor jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for medical device board advisor in the United States is $53.85, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $78.37 per hour, depending on experience, location, and employer.

What is a medical device board advisor?

Medical Device Board Advisors are experienced professionals who provide strategic guidance, industry insights, and expert advice to medical device companies, typically at the board or executive level. They help shape company direction, ensure regulatory compliance, support product development, and connect organizations with key industry contacts. Their expertise often spans areas such as clinical practice, regulatory affairs, commercialization, and risk management, which is crucial for navigating the complex medical device landscape. Advisors may serve on formal boards of directors or as part of advisory boards to offer objective perspectives and foster company growth.

What are the key skills and qualifications needed to thrive as a medical device board advisor?

To thrive as a Medical Device Board Advisor, you need extensive medical device industry experience, regulatory knowledge, and a background in business strategy or clinical practice. Familiarity with FDA regulations, ISO standards, and quality management systems, as well as experience with product development tools, is typically expected. Strategic thinking, strong communication, and the ability to build consensus are crucial soft skills for guiding executive teams and stakeholders. These skills and qualifications are important because they ensure effective oversight, compliance, and innovation in a highly regulated and competitive industry.

How does a medical device board advisor typically contribute to product development and regulatory strategy?

Medical Device Board Advisors play a crucial role in guiding product development teams on compliance with regulatory standards and best practices. They often collaborate closely with R&D, quality assurance, and regulatory affairs departments to provide strategic insights, anticipate industry trends, and mitigate risks. Advisors help shape the company's approach to FDA submissions, CE marking, and clinical evaluations, ensuring that new devices meet safety and efficacy requirements. Their expertise is especially valuable in navigating complex regulations and accelerating time-to-market while maintaining compliance.

What are popular job titles related to Medical Device Board Advisor jobs?

For Medical Device Board Advisor jobs, the most frequently searched job titles are:

Medical Device Decontamination SME

Bethesda, MD • On-site

Tunnell Government Services
See more jobs at Tunnell Government Servicesexternal

Full-time

Re-posted 21 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.
FDA CDRH - Medical Device Decontamination SME Position Description
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. Tunnell Government Services, Inc. is providing professional and scientific services to the CDRH with expert consultants with scientific expertise in the regulation and approval of medical devices.
Responsibilities:
  • Tunnell is seeking a candidate to provide expert consulting services to assist the CDRH with their regulatory responsibilities. This candidate should possess specific expertise, experience, and training in the field of decontamination/sterilization, as relevant to medical devices and device related combination products.
  • The primary focus of the role is to provide regulatory and technical support to CDRH in the review and disposition of submittals from the medical device decontamination/sterilization industry to include review of 510(k) submissions, consultations, Pre-Submission (Q-Sub) engagements, among others. The candidate will use a combination of technical and operational expertise along with extensive review of FDA guidance documents and standard test methods relevant to each product to conduct a review of each submission, with a goal of ensuring that the product is safe and effective
  • Participate in meetings and teleconferences, coordinate meetings with internal and external stakeholders related to marketing applications and pre-submissions
  • Support ancillary, prioritized activities in support of the agency, such as performing review of Medical Device Reporting (MDR) submittals
  • Develop written reviews and correspondence
  • Write detailed documents and reports

Skills and Qualifications:
  • The candidate must possess a bachelor's degree (BS in a scientific/technical discipline applicable to sterilization/decontamination)
  • An advanced degree (MS, PhD) in a related/applicable field is strongly preferred.
  • At least 15 years of experience is required (direct experience in decontamination/sterilization involving medical products)
  • Experience with FDA Sterilization/Decontamination Guidance and other US regulatory requirements and consensus standards (ISO, ANSI) for medical devices highly preferred.
  • Candidate must be able to apply knowledge of decontamination/sterilization to the assessment of medical devices. This must entail an advanced understanding of the various techniques and industry best practices involving technologies to include fumigants, radiation, use of heat/steam, disinfectants, and validation approaches, e.g., indicators.
  • The ability to read and interpret standards, as well as knowledge of validation and testing methods related to sterilization, biocompatibility, shelf life, and performance testing, is critical.
  • 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.

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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