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Medical Device Testing Jobs in Washington (NOW HIRING)

Ametek

Sr. Mechanical Engineer

Germantown, MD · On-site

$106K - $140K/yr

Support completion and deployment of a manufacturing cell for a medical device. * Develop and ... Hands-on experience building, testing, troubleshooting, and evaluating prototypes. * Experience ...

VB Spine

Staff Packaging Engineer

Leesburg, VA · On-site

Establish yourself as a thought leader in sterile and non-sterile medical device packaging while ... testing activities Why VB Spine? We believe in growing talent from within. At VB Spine, join a high ...

Ametek

Sr. Mechanical Engineer

Germantown, MD · On-site

$106K - $140K/yr

Support completion and deployment of a manufacturing cell for a medical device. * Develop and ... Hands-on experience building, testing, troubleshooting, and evaluating prototypes. * Experience ...

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Medical Device Testing information

See Washington salary details

$24

$41

$80

How much do medical device testing jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for medical device testing in Washington is $41.59, according to ZipRecruiter salary data. Most workers in this role earn between $28.03 and $52.02 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed for medical device testing?

To thrive in Medical Device Testing, you need a strong background in biomedical engineering, quality assurance, and regulatory compliance, often supported by a relevant degree. Hands-on experience with testing equipment, validation protocols, and familiarity with standards such as ISO 13485 and FDA guidelines are typically required. Attention to detail, analytical thinking, and clear documentation skills are essential soft skills for excelling in this field. These abilities ensure that devices meet safety and performance standards, protecting patient health and supporting company compliance.

What does medical device testing involve?

Professionals in Medical Device Testing typically spend their days conducting tests on new or existing medical devices to ensure they meet quality, safety, and regulatory standards. This often involves following strict protocols, documenting results accurately, and troubleshooting any performance or compliance issues that arise. Team members frequently collaborate with engineers, regulatory specialists, and manufacturing staff to ensure seamless product development and problem resolution. There may also be tasks related to preparing reports for regulatory submissions or participating in audits. This role offers the opportunity to make a real impact on patient safety while working in a collaborative, fast-paced environment.

What is medical device testing?

A Medical Device Testing job involves evaluating medical devices to ensure they meet regulatory standards, safety guidelines, and performance requirements. Professionals in this role conduct tests, analyze data, and document results to verify compliance with industry regulations such as FDA, ISO, and IEC standards. They work with engineers and regulatory teams to identify design flaws, improve product safety, and ensure reliability before market release. This job is crucial for preventing defects that could impact patient health and safety.

What are the most commonly searched types of Medical Device Testing jobs in Washington? The most popular types of Medical Device Testing jobs in Washington are:
What are popular job titles related to Medical Device Testing jobs in Washington? For Medical Device Testing jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Medical Device Testing jobs in Washington look for? The top searched job categories for Medical Device Testing jobs in Washington are:
What cities in Washington are hiring for Medical Device Testing jobs? Cities in Washington with the most Medical Device Testing job openings:
Medical Device Testing jobs near you
Infographic showing various Medical Device Testing job openings in Washington as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $86,513 per year, or $41.6 per hour.

Medical Device Decontamination SME

Tunnell Government Services

Bethesda, MD • On-site

Other

Posted 13 days ago

Job description

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.

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