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Fda Jobs in California, MD (NOW HIRING)

Industrial Resource Group

Operations Manager

Newburg, MD · On-site

$90K - $125K/yr

Ensure compliance with USDA Warehousing, FDA regulations, and company requirements. Ensure routine and preventative maintenance is performed on all equipment to maximize availability, operating ...

Recor Medical

Training Manager

California, MD · On-site

$134K - $154K/yr

Proven experience in adult education, learning, development, and/or training * 5 years' work experience or higher in education related field in medical device, pharmaceutical, biotech, or other FDA ...

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Fda information

What does an FDA professional do?

An FDA professional works for the U.S. Food and Drug Administration, a federal agency responsible for protecting public health by ensuring the safety and efficacy of drugs, medical devices, food, cosmetics, and other products. Their roles can include reviewing and approving new drugs and medical devices, conducting inspections, enforcing regulations, and providing guidance to industries. FDA professionals may also work in research, policy development, and public outreach to ensure that products meet regulatory standards and are safe for consumer use.

What are the key skills and qualifications needed to thrive as an FDA Regulatory Affairs Specialist, and why are they important?

To thrive as an FDA Regulatory Affairs Specialist, you need a strong background in life sciences, regulatory guidelines, and compliance, usually supported by a relevant degree such as pharmacy, biology, or chemistry. Familiarity with regulatory submission systems, FDA regulations (such as 21 CFR), and certifications like RAC (Regulatory Affairs Certification) are highly beneficial. Attention to detail, strong analytical thinking, and effective communication skills help professionals navigate complex regulations and collaborate with cross-functional teams. These competencies ensure that products meet legal requirements and safety standards, facilitating successful approvals and market access.

What are some typical challenges faced by professionals working at the FDA, and how can they be managed?

Professionals at the FDA often navigate complex regulatory requirements, tight deadlines, and the need to balance public health priorities with industry innovation. Collaborating across multidisciplinary teams and staying updated on evolving scientific data are essential parts of the role. Adapting to frequent changes in policy and handling high volumes of submissions can be demanding, but leveraging strong communication skills and seeking mentorship within the agency can help manage these challenges effectively.

What is the difference between Fda vs Food Scientist?

AspectFdaFood Scientist
Required CredentialsTypically a degree in health, science, or related field; certifications varyBachelor's or master's in food science, microbiology, or related
Work EnvironmentRegulatory agencies, laboratories, inspection sitesFood manufacturing facilities, laboratories, research settings
Employer & Industry UsageU.S. Food and Drug Administration, government agenciesFood companies, research institutions, government agencies
Common Search & Comparison IntentUnderstanding regulatory roles, compliance, and enforcementFood safety, product development, research

While both Fda professionals and Food Scientists work within the food industry, Fda roles focus on regulation, compliance, and enforcement of food safety laws, often within government agencies. Food Scientists primarily engage in research, product development, and ensuring food quality in manufacturing settings. The two careers overlap in food safety knowledge but differ in their primary responsibilities and work environments.

What qualifications do you need to work for the Food and Drug Administration?

To work for the Food and Drug Administration (FDA), candidates typically need a bachelor's degree in a relevant field such as science, engineering, or public health. For certain positions, advanced degrees or specialized certifications may be required, along with relevant work experience and knowledge of regulatory processes and compliance standards.

What are the most commonly searched types of Fda jobs in California, MD?

The most popular types of Fda jobs in California, MD are:

What cities near California, MD are hiring for Fda jobs?

Cities near California, MD with the most Fda job openings:

Fda jobs near you
Infographic showing various Fda job openings in California, MD as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution.

Associate Director, Global Medical & Promotional Regulatory Affairs

Scorpion Therapeutics

California, MD • On-site

$160 - $240/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago

Job description

Associate Director, Global Medical and Promotional Regulatory Affairs

Essential Job Functions
  • Lead the Promotional Materials Review Committee (PMRC) for assigned products/therapeutic areas in the US; provide input on concepts and draft promotional materials to meet FDA promotional regulations, corporate standards/policies, and business objectives.
  • Serve as Promotional Regulatory Affairs lead for new product launches as needed (contributions to US Core launch team).
  • Provide regulatory advice and support; lead PMRC process, manage review/approval of promotional materials, ensure compliance with FDA regulations, and submit materials to OPDP in a timely fashion.
  • Chair review meetings; lead discussion, collaborate with cross-functional reviewers to determine next steps/approval status.
  • Ensure submission content, quality, accuracy, and format comply with internal policies/procedures and FDA guidance/regulations.
  • Partner with Regulatory, Medical Affairs, Legal/Compliance, Marketing, and other departments to ensure thorough, timely, efficient material review.
  • Provide regulatory support for Medical Affairs Review Committee (MARC) and publications review.
  • Contribute to regulatory strategy for the assigned Global Regulatory team.
  • Provide guidance on new marketing concepts and promotional tactics.
  • Lead FDA/OPDP interactions, including advisory comment submissions for full approval and accelerated approval products.
  • Stay current on evolving FDA regulations/interpretations, enforcement letters, and policy issues; communicate FDA perspective and recommend policy/process changes.
Required/Preferred Education and Licences
  • BS/BA in a scientific discipline or equivalent plus substantial increasingly responsible pharmaceutical industry experience; direct advertising/promotional material review experience required. PharmD or other advanced scientific degree strongly preferred.
  • Strong understanding of FDA regulations and guidelines.
  • Strong judgment and decision-making; excellent collaboration and verbal/written communication.
US Candidates Only (Pay and Benefits)
  • Base pay range: $160,000–$240,000.
  • Eligible for discretionary annual cash bonus/incentive and discretionary equity grants.
  • Eligible for medical, dental, vision, 401k, and flexible paid vacation.
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