ZipRecruiter

Log In

1

Fda Scientist Jobs (NOW HIRING)

Orano

Quality Scientist

Plano, TX · On-site

... FDA, EMA, and global regulatory expectations. Success requires exceptional analytical acumen ... Bachelor's of Science (or higher) in Chemistry or other related field * 7+ years experience in ...

Alakaina Family of Companies

Scientist

San Antonio, TX · On-site

Bering-Alaka`ina Holdings (BAH) is looking for Scientist to perform services that impact a Combat ... Experience with in vitro testing of pharmaceuticals for FDA approval. * Experience developing high ...

MeriCal, LLC

Nutrition Scientist

Orange, CA · On-site

$120K - $140K/yr

Review product labels are marketing materials for FDA compliance. * Develop dietary supplement ... Access scientific data for quality and compliance risks. * Guide research based on claim(s) and ...

Actalent

Applications Food Scientist

Racine, WI · On-site

Operate within FDA, FSMA, and Global Food Safety Initiative (GFSI) requirements to ensure food ... Degree in food science or a related field of study. * Technical experience and a demonstrated track ...

Actalent

Applications Food Scientist

Racine, WI

Operate within FDA, FSMA, and Global Food Safety Initiative (GFSI) requirements to ensure food ... Degree in food science or a related field of study. * Technical experience and a demonstrated track ...

Kelly Services

Senior Scientist

Lincoln, NE

$79K - $123K/yr

Support regulatory submissions and compliance efforts involving FDA and USDA requirements for veterinary biologics. * Contribute to continuous improvement initiatives and scientific problem-solving ...

Kelly Services

Senior Scientist

Lincoln, NE · On-site

$79K - $123K/yr

Support regulatory submissions and compliance efforts involving FDA and USDA requirements for veterinary biologics. * Contribute to continuous improvement initiatives and scientific problem-solving ...

PMHD

Clinical Lab Scientist

Brawley, CA · On-site

... 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 ...

next page

Showing results 1-20

All JobsFda Scientist Jobs

Fda Scientist information

See salary details

$50.5K

$111.3K

$137.5K

How much do fda scientist jobs pay per year?

As of Jul 8, 2026, the average yearly pay for fda scientist in the United States is $111,343.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,500.00 and $137,000.00 per year, depending on experience, location, and employer.

What is an FDA Scientist job?

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 is the highest paying job at the FDA?

The highest paying jobs at the FDA are typically senior leadership roles such as the Commissioner of Food and Drugs or Deputy Commissioner, as well as senior scientific and medical directors. These positions often require advanced degrees, extensive experience, and leadership skills, and they can earn salaries exceeding $200,000 annually, with additional benefits and bonuses.

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 or those with advanced degrees can earn higher salaries, especially with specialized skills or supervisory roles.

Is it hard to get hired by the FDA?

Getting hired as an FDA scientist can be competitive due to the specialized qualifications required, such as relevant degrees and experience in regulatory science or related fields. Candidates often need to pass rigorous screening processes, including interviews and background checks, and may require certifications or knowledge of FDA regulations. Strong technical skills and familiarity with the agency's procedures improve hiring prospects.

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.

Does the FDA employ scientists?

Yes, the FDA employs scientists in various roles such as biologists, chemists, and pharmacologists to evaluate the safety and effectiveness of medical products, foods, and cosmetics. These scientists often work in laboratories, conduct research, and analyze data to support regulatory decisions, typically requiring relevant degrees and certifications. Their work is essential to ensuring public health and safety standards are met.
More about Fda Scientist jobs
What cities are hiring for Fda Scientist jobs? Cities with the most Fda Scientist job openings:
What are the most commonly searched types of Fda Scientist jobs? The most popular types of Fda Scientist jobs are:
What states have the most Fda Scientist jobs? States with the most job openings for Fda Scientist jobs include:
What job categories do people searching Fda Scientist jobs look for? The top searched job categories for Fda Scientist jobs are:
Fda Scientist jobs near you

Quality Scientist

Orano

Plano, TX • On-site

Full-time

Posted 2 days ago

Job description

Description
Orano Med Theranostics
Orano Med has developed new processes for producing high-purity lead-212, a rare radioactive isotope. Lead-212 is currently at the heart of promising research projects in nuclear medicine to develop new treatments against cancer. The innovative approach, known as targeted alpha therapy (TAT), recognizes and destroys cancer cells while limiting the impact on nearby healthy cells.
Orano Med LLC has opening for Quality Scientist in Plano, TX.
This role ensures the integrity, reliability, and regulatory compliance of analytical methods and their transfers used for drug product testing from early development through Phase 2 clinical manufacturing. The Quality Scientist partners closely with QC, Analytical Development, Manufacturing, and QA teams. Using strong scientific judgment and GMP expertise, this position leads investigations, evaluates analytical trends, drives effective CAPAs, and ensures method qualification, validation, and transfer activities meet FDA, EMA, and global regulatory expectations. Success requires exceptional analytical acumen, meticulous attention to detail, and the ability to translate complex laboratory and process data into compliant, practical solutions that protect product quality and patient safety.
Key Responsibilities
  • Perform thorough technical review of QC analytical data, including raw data, chromatograms, calculations, audit trails, and reports to verify accuracy, data integrity, and method compliance while identifying trends.
  • Lead and support analytical method qualification, validation, and transfer activities, including protocol review, data evaluation, receiving site alignment, and adherence to ICH Q2/Q14, FDA, and EMA guidelines.
  • Drive continuous improvement of the analytical qualification/validation program through data trending, method performance monitoring, and initiatives to enhance robustness and reduce variability.
  • Conduct scientifically sound investigations of analytical deviations, OOS/OOT results, and nonconformances, ensuring robust root cause analysis and effective CAPA implementation.
  • Provide technical review and approval of method transfer packages, validation documents, and associated data to ensure regulatory and internal compliance.
  • Assess manufacturing processes, method performance, and R&D recommendations to identify risks, propose improvements, and support method optimization and lifecycle management.
  • Execute complex quality and analytical tasks to deliver consistent, high-quality data, methods, and processes across the product development lifecycle.
  • Perform additional duties as assigned to advance quality system maturity, analytical readiness, and regulatory compliance.

Requirements
All candidates must meet the following minimum requirements in order to be considered for this opportunity. Candidates who exceed minimum qualifications may be considered for a higher-level position.
Minimum Qualifications
  • Bachelor's of Science (or higher) in Chemistry or other related field
  • 7+ years experience in Pharmaceuticals
  • 5+ years experience as a QC analyst or Method Development

Preferred Skills & Competencies
  • Strong experience performing technical review of Analytical Data
  • Experience writing & reviewing SOPs, Protocols, Technical Reports and other associated GMP documentation
  • In-depth knowledge of cGMP, GLP, FDA/EMA regulations, ICH guidelines, USP/EP pharmacopeial methods, and data integrity principles.
  • Proficient in Microsoft Office, Excel, and Power Point
  • Excellent technical writing and verbal communication skills.
  • Strong organization skills and attention to detail.
  • Able to easily switch between multiple ongoing projects, adjusting priorities based on business needs.

Apply