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Remote Fda Jobs in Maryland (NOW HIRING)

Wearlinq is reimagining ambulatory cardiac monitoring with the first FDA-cleared, real-time, six ... A rare opportunity for remote techs is now open! Clinician must be able to submit comprehensive ...

Wearlinq is reimagining ambulatory cardiac monitoring with the first FDA-cleared, real-time, six ... A rare opportunity for remote techs is now open! Clinician must be able to submit comprehensive ...

Food and Drug Administration (FDA). This position is contingent upon award. This position is remote with periodic on-site presence at Silver Spring, MD. Clearance Requirement: Current or ability to ...

$44K/yr

Wearlinq is reimagining ambulatory cardiac monitoring with the first FDA-cleared, real-time, six ... Benefits: * Optional Remote work opportunity * 401(k) * Dental insurance * Health insurance

Wearlinq is reimagining ambulatory cardiac monitoring with the first FDA-cleared, real-time, six ... Benefits: * Optional Remote work opportunity * 401(k) * Dental insurance * Health insurance

Central Monitor

Bethesda, MD ยท Remote

$18.25 - $19.50/hr

Applies a thorough understanding of regulatory (FDA requirements, GCPs/ICH guidelines), data ... This role is fully remote to those in/willing to relocate to Maryland, Virginia, or Washington D.C.

Central Monitor

Bethesda, MD ยท On-site +1

$85K - $115K/yr

Applies a thorough understanding of regulatory (FDA requirements, GCPs/ICH guidelines), data ... This role is fully remote to those in/willing to relocate to Maryland, Virginia, or Washington D.C.

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Remote Fda information

See Maryland salary details

$25.9K

$88.4K

$173.9K

How much do remote fda jobs pay per year?

As of Sep 2, 2026, the average yearly pay for remote fda in Maryland is $88,354.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,332.00 and $114,626.00 per year, depending on experience, location, and employer.

What is a remote FDA?

A Remote FDA job typically involves working for or with the U.S. Food and Drug Administration (FDA) from a remote location. These roles can include regulatory affairs, compliance, medical writing, research, and reviewing submissions for drug and medical device approvals. Remote FDA jobs require knowledge of FDA regulations, strong analytical skills, and experience in healthcare, pharmaceuticals, or related fields. They offer flexibility while maintaining high regulatory standards and ensuring public health and safety.

What are the typical daily responsibilities of a remote FDA compliance specialist?

A Remote FDA Compliance Specialist generally reviews and updates regulatory documents, conducts virtual audits, and monitors company practices for FDA compliance. They regularly collaborate with cross-functional teams, such as quality assurance, legal, and product development, to provide guidance on regulatory requirements and respond to compliance queries. Additionally, they prepare and submit necessary reports, maintain records for inspections, and stay current on evolving regulations. This remote structure allows flexibility but also demands excellent organization, communication, and self-discipline to ensure all deadlines and compliance standards are met.

What are the key skills and qualifications needed to thrive in the remote FDA position, and why are they important?

To excel as a Remote FDA Compliance Specialist, you need in-depth knowledge of FDA regulations, quality assurance procedures, and a background in life sciences or a related field. Proficiency in using compliance management systems, electronic document management tools, and relevant certifications such as RAC (Regulatory Affairs Certification) are often required. Exceptional attention to detail, self-motivation, and strong written and verbal communication skills are vital for remote collaboration and thorough documentation. These abilities ensure regulatory adherence, minimize compliance risks, and facilitate effective remote teamwork within the pharmaceutical or medical device industry.

What jobs can I do completely remotely as a remote FDA?

A remote FDA typically refers to a Food and Drug Administration-related role that can be performed remotely, such as regulatory affairs specialists, quality assurance managers, or compliance analysts. These positions often require knowledge of regulations, strong communication skills, and familiarity with digital tools for document review and reporting, allowing work to be done entirely online. However, some roles may require occasional on-site visits or inspections depending on the specific job and employer policies.

What are the most commonly searched types of Fda jobs in Maryland?

The most popular types of Fda jobs in Maryland are:

What cities in Maryland are hiring for Remote Fda jobs?

Cities in Maryland with the most Remote Fda job openings:

Infographic showing various Remote Fda job openings in Maryland as of August 2026, with employment types broken down into 91% Full Time, and 9% Part Time. Highlights an 9% In-person, and 91% Remote job distribution, with an average salary of $88,354 per year, or $42.5 per hour.

Full-time, Part-time

Posted 21 days ago


Job description

Medical Physics Subject Matter Expert (Full-Time, Remote Contractor)

The FDA Center for Devices and Radiological Health (CDRH), Office of Radiological Health, Division of Radiological Imaging and Radiation Therapy Devices (DHT8C), is seeking a full-time or part-time, fully remote contractor to provide specialized technical and regulatory support for the review of radiation oncology, radiological imaging, nuclear medicine, and radiation-emitting products.

Key Responsibilities

  • Conduct technical reviews of medical device regulatory submissions, including 510(k), PMA, Pre-IDE, IDE, and 513(g) submissions.
  • Provide expert support for postmarket and compliance activities, including Medical Device Reports (MDRs), recalls, Establishment Inspection Reports (EIRs), Electronic Product Radiation Control (EPRC) issues, and trade complaints.
  • Evaluate radiation oncology, nuclear medicine, and radiologic imaging technologies for safety, effectiveness, performance, and clinical application.
  • Review dosimetry methodologies, software systems, and dose calculation algorithms associated with nuclear medicine and radiopharmaceutical therapy devices.
  • Provide subject matter expertise in radiation oncology physics, including quality assurance, external beam radiation therapy, and brachytherapy.
  • Interpret and apply relevant FDA regulations, guidance documents, consensus standards, and risk management principles to support regulatory decision-making.

Minimum Qualifications

  • Master's degree or PhD in Medical Physics or a closely related scientific discipline.
  • 5-10 years of professional experience in medical physics.
  • Demonstrated expertise in radiation oncology physics, including quality assurance, external beam therapy, and brachytherapy.
  • Extensive experience with dosimetry, nuclear medicine devices, and radiopharmaceutical therapy dose calculation software.
  • Working knowledge of applicable FDA medical device regulations, guidance documents, relevant sections of 21 CFR, and recognized national and international consensus standards applicable to radiation oncology, nuclear medicine, and radiologic imaging devices.
  • U.S. Citizen or Lawful Permanent Resident (Green Card Holder).

Preferred Qualifications

  • American Board of Radiology (ABR) certification in Medical Physics.
  • Experience supporting FDA-regulated medical devices, including premarket review, compliance, quality systems, and postmarket activities.
  • Familiarity with FDA-recognized standards and guidance documents related to radiation-emitting products, medical imaging systems, radiation therapy devices, software, and cybersecurity.

Position Type: Full-Time Contractor
Work Location: Fully Remote (U.S.-Based)
Organization Supported: FDA CDRH, Office of Radiological Health, Division of Radiological Imaging and Radiation Therapy Devices (DHT8C)

Must be a US Citizen or a Green Card Holder.