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Regulatory Affairs Scientist (Devices)

Department of Defense - Fort Detrick, Maryland

Posted Jun 11, 2026

Benefits

Parental leave
Not verified
Non-birth-parent leave
Not verified
Family-building benefits
  • Fertility benefits: Not verified
  • Adoption assistance: Not verified
  • Surrogacy assistance: Not verified
Mental health support
Not verified
Relocation assistance
Not verified
Childcare support
Not verified
Learning budget
Not verified
Verification
Not verified
Salary
$122K-$187K From the posting source checked Jun 20, 2026
401(k) match
Not verified

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Market context

U.S. role benchmark (BLS OEWS)
$61,842 U.S. median for this role
Projected growth (BLS Employment Projections)
+1.9% - Slower

150% above the BLS role benchmark for operations aggregate.

Matched to SOC 11-1021 - Operations aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function
Operations From the posting source checked Jun 20, 2026
Seniority
Mid From the posting source checked Jun 20, 2026

Schedule

Shift type
Not verified
Weekend work
Not verified

Application

Cover letter
Not verified
Assessment
Not verified
Deadline
Jun 18, 2026 From the posting source checked Jun 20, 2026

Where they hire

Hires in: MD From the posting source checked Jun 20, 2026

About this role

Regulatory Affairs Scientist (Devices) Fort Detrick, Maryland Summary About the Position: MRDC is now part of the Defense Health Agency (DHA) Research & Development (R&D). We are themedical materiel developer, with responsibility for medical research, development and acquisition. Ourexpertise in these critical areas helps establish and maintain the capabilities the military needs to remainready and lethal on the battlefield. Please visit our website https://mrdc.health.mil/ This is a Direct Hire Solicitation Duties Develop and implement comprehensive regulatory affairs strategies for advanced 'tech base' medical devices and diagnostic products to ensure mission-critical compliance from early development Establish and maintain Quality Management Systems specifically tailored for the lifecycle of advanced medical diagnostics and early-stage technological innovations Lead Medical Devices branch personnel, providing professional mentorship while managing high-priority project portfolios to meet operational milestones Direct all Food and Drug Administration-regulated activities across the development pipeline, ensuring organizational adherence to federal statutes and agency mandates Oversee the execution of nonclinical and clinical studies, ensuring all research activities strictly adhere to Good Clinical Practices and internal protocols Manage manufacturing and testing operations to ensure full compliance with Good Manufacturing Practices and Quality Management System Regulations Align product development plans with both pre-market and post-market Food Drug Administration requirements to facilitate efficient device clearance, approval, and long-term surveillance Execute medical device classification processes and conduct risk assessments to categorize Significant Risk and Non-significant Risk research studies Lead the preparation and strategic management of regulatory submissions, including Investigational Device Exemptions, premarket notifications, Deovo and Premarket approval Perform expert

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