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Remote Fda Jobs in California (NOW HIRING)

Tempus

Senior Quality Engineer

Redwood City, CA · On-site +1

Be involved in the medical device software design controls activities, in accordance with the FDA ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...

DivIHN

Sr SW Test Development Engineer - Remote

San Diego, CA · On-site +1

$117K - $152K/yr

San Diego, CA (Remote) Ocasional office visits required only for hardware pickup and meetings in ... an FDA-regulated quality environment. * Proactively identify and mitigate risks and resolve ...

Vaxcyte

Associate Director, Regulatory CMC

San Carlos, CA · On-site +1

$180K - $210K/yr

Advanced knowledge in regulatory (FDA, EMA, Health Canada and ICH) guidelines Reports to: Executive Director, CMC Regulatory Location: San Carlos, CA / US Remote Work Arrangement: Remote Compensation:

BigHat Biosciences

SharePoint Consultant

San Mateo, CA · On-site +1

... submitted to FDA or ex-US health authorities), replacing manual email-based review chains ... Ability to work independently, manage deliverables across a remote engagement, and communicate ...

BigHat Biosciences

SharePoint Consultant

San Mateo, CA · On-site +1

... submitted to FDA or ex-US health authorities), replacing manual email-based review chains ... Ability to work independently, manage deliverables across a remote engagement, and communicate ...

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Showing results 1-20

All JobsFda JobsRemote Fda JobsRemote Fda Jobs in California

Remote Fda information

See California salary details

$25.5K

$86.8K

$170.9K

How much do remote fda jobs pay per year?

As of Aug 25, 2026, the average yearly pay for remote fda in California is $86,801.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,430.00 and $112,611.00 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 California?

The most popular types of Fda jobs in California are:

What are popular job titles related to Remote Fda jobs in California?

For Remote Fda jobs in California, the most frequently searched job titles are:

What job categories do people searching Remote Fda jobs in California look for?

The top searched job categories for Remote Fda jobs in California are:

What cities in California are hiring for Remote Fda jobs?

Cities in California with the most Remote Fda job openings:

Remote Fda jobs near you
Infographic showing various Remote Fda job openings in California as of August 2026, with employment types broken down into 53% Full Time, and 47% Part Time. Highlights an 100% Remote job distribution, with an average salary of $86,801 per year, or $41.7 per hour.

Regulatory Affairs Consultant - Fully Remote | Upto $170/hr

Mercor

San Francisco, CA • Remote

$170/hr

Full-time

Posted 2 days ago

New

Job description

About the job

Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey.

Position: Clinical Regulatory Expert
Type: Contract
Compensation: $130–$170/hour
Location: Remote
Commitment: 20–25 hours/week

Role Responsibilities

  • Validate clinical data rooms and documents against FDA evidentiary standards and formatting expectations.
  • Author FDA information requests and model responses. Design prompts, golden outputs, and rubrics to quantify AI agent capabilities.
  • Ensure compliance with deliberate defects testing regulatory judgment.
  • Work independently and asynchronously to meet deadlines and improve AI model performance.

Qualifications

Must-Have

  • 5+ years of experience in regulatory roles.
  • MD, PhD, PharmD, or equivalent.
  • Experience reviewing or responding to FDA information requests across CMC, patient-level data, investigator qualifications, and biomarker or endpoint evidence.
  • No conflict of interest with a current federal employer.

Preferred

  • 10–25 years of experience.
  • Direct FDA review experience preferred over sponsor-side liaison work.

Application Process (Takes 20–30 mins to complete)

  • Upload resume
  • AI interview based on your resume
  • Submit form

Resources & Support

  • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome
  • For any help or support, reach out to: support@mercor.com

PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.