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Medical Device Reporting Jobs in Washington (NOW HIRING)

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 ... Generate, review, and approve validation summary reports and supporting documentation for ...

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 ... Generate, review, and approve validation summary reports and supporting documentation for ...

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All JobsMedical Device Reporting JobsMedical Device Reporting Jobs in Washington

Medical Device Reporting information

See Washington salary details

$14

$22

$29

How much do medical device reporting jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for medical device reporting in Washington is $22.22, according to ZipRecruiter salary data. Most workers in this role earn between $19.62 and $23.94 per hour, depending on experience, location, and employer.

What is medical device reporting?

Medical device reporting is the process by which manufacturers, importers, and device user facilities notify regulatory authorities, such as the FDA, about certain adverse events and product problems involving medical devices. This reporting system helps monitor the safety and effectiveness of medical devices once they are on the market. The information collected can lead to recalls, safety alerts, or other actions to protect public health.

What are the key skills and qualifications needed to thrive in medical device reporting, and why are they important?

To excel in Medical Device Reporting, you need a solid understanding of regulatory requirements, data analysis, and healthcare compliance, often supported by a degree in life sciences or a related field. Familiarity with regulatory databases such as FDA’s MAUDE, electronic reporting systems, and quality management software is typically required. Strong attention to detail, analytical thinking, and effective written communication help ensure accurate and timely reporting. These skills are critical for maintaining regulatory compliance, protecting patient safety, and supporting product quality in the medical device industry.

What are some typical challenges faced by professionals in medical device reporting, and how can they be managed?

Professionals working in Medical Device Reporting often encounter challenges such as managing tight regulatory deadlines, ensuring complete and accurate documentation, and staying current with evolving global reporting requirements. Effective time management, attention to detail, and regular training on regulatory updates are essential for success in this role. Collaboration with quality assurance, regulatory affairs, and clinical teams also helps ensure timely and compliant submissions, minimizing the risk of non-compliance.

What is the difference between Medical Device Reporting vs Medical Device Technician?

AspectMedical Device ReportingMedical Device Technician
Required CredentialsRegulatory knowledge, often a background in healthcare or regulatory affairsTechnical skills, certifications in medical equipment maintenance or biomedical technology
Work EnvironmentRegulatory agencies, healthcare compliance departmentsHospitals, clinics, biomedical equipment service centers
Employer & Industry UsageUsed by medical device manufacturers, healthcare providers, and regulatory bodiesEmployers include hospitals and biomedical service companies
Common Search & Comparison IntentUnderstanding regulatory roles in medical device safetyTechnical maintenance and repair of medical devices

Medical Device Reporting focuses on regulatory compliance and reporting adverse events, while Medical Device Technicians handle the maintenance and repair of medical equipment. Both roles are essential in the medical device industry but serve different functions within healthcare and regulatory environments.

What are popular job titles related to Medical Device Reporting jobs in Washington?

For Medical Device Reporting jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Medical Device Reporting jobs in Washington look for?

The top searched job categories for Medical Device Reporting jobs in Washington are:

What cities in Washington are hiring for Medical Device Reporting jobs?

Cities in Washington with the most Medical Device Reporting job openings:

Medical Device Reporting jobs near you
Infographic showing various Medical Device Reporting job openings in Washington as of August 2026, with employment types broken down into 41% Full Time, and 59% Contract. Highlights an 85% In-person, and 15% Hybrid job distribution, with an average salary of $46,224 per year, or $22.2 per hour.

Medical Device Decontamination SME

Tunnell Government Services

Bethesda, MD

Full-time

Re-posted 3 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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