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Fda Scientist Jobs in California (NOW HIRING)

Nutrition Scientist

Orange, CA · On-site

$120K - $140K/yr

Evaluate scientific literature to support structure-function claims ... Ensure claims are truthful, not misleading, and FDA compliant. Label & Compliance Review: * Review ...

... and FDA policies and procedures. Conduct chemical analysis of body fluids and collect and study ... Must have Bachelor of Science in Medical Technology/Clinical Laboratory Science or equivalent and ...

... and FDA policies and procedures. Conduct chemical analysis of body fluids and collect and study ... Must have Bachelor of Science in Medical Technology/Clinical Laboratory Science or equivalent and ...

FDA Senior Analyst

Los Angeles, CA · On-site

$105 - $120/hr

Job Summary Viking Cruises is seeking a Financial Data Analytics (FDA) Senior Financial Analyst ... Bachelor's degree in Accounting, Computer Science or related field * Minimum of 2+ years of ...

Senior Biocompatibility Scientist II

Santa Clara, CA · On-site

$107K - $146K/yr

Senior Biocompatibility Scientist II Working at Abbott At Abbott, you can do work that matters ... 14971, FDA Biocompatibility Guidance, and Regulation (EU) 2017/745. You willleverageyour ...

Beverage Scientist

Hayward, CA · On-site

$95K - $110K/yr

... FDA regulations and policies. • Works across functions and communicates with all functional and operating groups on labeling and compliance matters. • Ability to travel to any location where the ...

... FDA regulations and policies. • Works across functions and communicates with all functional and operating groups on labeling and compliance matters. • Ability to travel to any location where the ...

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Showing results 1-20

Fda Scientist information

See California salary details

$49.8K

$109.9K

$135.7K

How much do fda scientist jobs pay per year?

As of Sep 3, 2026, the average yearly pay for fda scientist in California is $109,885.00, according to ZipRecruiter salary data. Most workers in this role earn between $93,300.00 and $135,200.00 per year, depending on experience, location, and employer.

What is an FDA Scientist?

An FDA Scientist is a researcher or regulatory expert responsible for evaluating the safety, efficacy, and quality of pharmaceutical drugs, medical devices, biologics, and food products. They conduct laboratory research, review clinical trial data, and assess regulatory submissions to ensure compliance with federal laws and guidelines. FDA Scientists play a critical role in protecting public health by making science-based decisions on product approvals and safety standards.

What types of projects and responsibilities can I expect as an FDA Scientist?

As an FDA Scientist, you'll typically be involved in reviewing data from clinical trials, conducting laboratory research, evaluating the safety and efficacy of pharmaceuticals or medical devices, and preparing reports for regulatory submissions. You'll collaborate closely with multidisciplinary teams including chemists, statisticians, and regulatory specialists to ensure scientific rigor and adherence to federal standards. Some days may involve detailed data analysis, while others could require participating in cross-team meetings or interacting with external stakeholders. This dynamic environment offers opportunities to contribute to important public health decisions and develop specialized expertise over time.

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

To thrive as an FDA Scientist, you need a solid background in biology, chemistry, pharmacology, or a related scientific field, typically supported by at least a bachelor's or advanced degree. Familiarity with regulatory submission systems, laboratory information management systems (LIMS), and relevant certifications such as Good Laboratory Practice (GLP) or Good Clinical Practice (GCP) is important. Strong analytical thinking, attention to detail, and effective communication skills help you excel when collaborating with colleagues and presenting findings. These abilities ensure accurate data review and regulatory compliance, which are crucial for advancing public health and safety.

How much do FDA scientists make?

FDA scientists typically earn between $70,000 and $130,000 annually, depending on experience, education, and location. Entry-level positions often start around $70,000, while experienced scientists with advanced degrees can earn higher salaries, especially in supervisory or specialized roles.

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

The most popular types of Fda Scientist jobs in California are:

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

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

Infographic showing various Fda Scientist job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $109,885 per year, or $52.8 per hour.

Regulatory Affairs Specialist (FDA, DEA )

BaRupOn LLC

Irvine, CA • On-site

$70 - $90/hr

Other

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Job description

Job Summary

The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn’s pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audits, and staying ahead of evolving federal and state regulations related to pharmaceuticals, medical devices, and controlled substances.

Key Responsibilities
  • Prepare and manage FDA submissions (e.g., drug listings, establishment registrations, 503A/503B updates)
  • Oversee and renew DEA registrations, inventory records, and security documentation
  • Maintain state pharmacy, medical device, and wholesale distribution licenses
  • Track regulatory changes affecting compounding, controlled substances, and labeling requirements
  • Support internal audits, site inspections, and responses to 483s or warning letters
  • Coordinate with Quality Assurance on SOP compliance, change controls, and deviation reports
  • Serve as point of contact with federal and state regulatory agencies
  • Document and file compliance records and ensure timely reporting
Qualifications
  • Associate degree in Life Sciences, Regulatory Affairs, or related field (Bachelor’s preferred)
  • 2–4 years of regulatory or compliance experience in pharmaceuticals, biotech, or medical devices
  • Working knowledge of FDA regulations (21 CFR Parts 210, 211, 820) and DEA requirements
  • Strong writing, documentation, and organizational skills
  • Familiarity with electronic submission systems, labeling requirements, and drug master files
Preferred Skills
  • Experience in sterile or non-sterile compounding (503A or 503B environments)
  • Knowledge of NABP license portals, MedWatch reporting, or REMS programs
  • Regulatory Affairs Certification (RAC) or DEA compliance training (preferred)
  • Experience responding to FDA inspections, audits, or state pharmacy board requests
Benefits
  • Health, dental, and vision insurance
  • 401(k) with employer match
  • Paid time off and holidays
  • Regulatory training and continuing education support
  • Advancement opportunities into QA/RA leadership roles
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