... and biologic products. This position is designated as an SES Equivalent position and is covered under the FDA Title 21 Executive Performance Management System and identified as a public filing ...
... and biologic products. This position is designated as an SES Equivalent position and is covered under the FDA Title 21 Executive Performance Management System and identified as a public filing ...
... of chemical, biological, radiological, and nuclear (CBRN) accidents, incidents and attacks ... These are products which are regulated by FDA's Center for Devices and Radiological Health (CDRH ...
... of chemical, biological, radiological, and nuclear (CBRN) accidents, incidents and attacks ... These are products which are regulated by FDA's Center for Devices and Radiological Health (CDRH ...
FDA regulatory engagement and product approval activities The candidate will work closely with ... Biology, Regulatory Affairs, or a related scientific discipline. * Advanced degree (M.S., Pharm.D ...
Quick apply
FDA regulatory engagement and product approval activities The candidate will work closely with ... Biology, Regulatory Affairs, or a related scientific discipline. * Advanced degree (M.S., Pharm.D ...
FDA regulatory engagement and product approval activities The candidate will work closely with ... Biology, Regulatory Affairs, or a related scientific discipline. * Advanced degree (M.S., Pharm.D ...
FDA regulatory engagement and product approval activities The candidate will work closely with ... Biology, Regulatory Affairs, or a related scientific discipline. * Advanced degree (M.S., Pharm.D ...
... biology technologies. The associate will handle all phases of complex patent disputes Hatch-Waxman ... Advise clients on FDA regulatory interfaces, Orange Book practice, and CMC-related issues impacting ...
Quick apply
... biology technologies. The associate will handle all phases of complex patent disputes Hatch-Waxman ... Advise clients on FDA regulatory interfaces, Orange Book practice, and CMC-related issues impacting ...
Bioassay Researcher
Silver Spring, MD · On-site
$85K - $141K/yr
Establish new analytical methods to evaluate the biological activity of biotechnology products ... with FDA laboratory standards. * Assist with laboratory inventory management, procurement ...
Bioassay Researcher
Silver Spring, MD · On-site
$85K - $141K/yr
Establish new analytical methods to evaluate the biological activity of biotechnology products ... with FDA laboratory standards. * Assist with laboratory inventory management, procurement ...
Bioassay Researcher
Silver Spring, MD · On-site
$85K - $141K/yr
Establish new analytical methods to evaluate the biological activity of biotechnology products ... with FDA laboratory standards. * Assist with laboratory inventory management, procurement ...
Bioassay Researcher
Silver Spring, MD · On-site
$85K - $141K/yr
Establish new analytical methods to evaluate the biological activity of biotechnology products ... with FDA laboratory standards. * Assist with laboratory inventory management, procurement ...
BTO is a unique technical office that leverages the power of biology as a technology to develop ... Experience interfacing with the FDA, NIH, or other regulatory/health-focused government agencies.
BTO is a unique technical office that leverages the power of biology as a technology to develop ... Experience interfacing with the FDA, NIH, or other regulatory/health-focused government agencies.
BTO is a unique technical office that leverages the power of biology as a technology to develop ... Experience interfacing with the FDA, NIH, or other regulatory/health-focused government agencies.
BTO is a unique technical office that leverages the power of biology as a technology to develop ... Experience interfacing with the FDA, NIH, or other regulatory/health-focused government agencies.
Training Manager (ITS17) Custom Computer Programming Services
Silver Spring, MD · On-site
$119K - $120K/yr
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
Training Manager (ITS17) Custom Computer Programming Services
Silver Spring, MD · On-site
$119K - $120K/yr
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
BTO is a unique technical office that leverages the power of biology as a technology to develop ... Experience interfacing with the FDA, NIH, or other regulatory/health-focused government agencies.
BTO is a unique technical office that leverages the power of biology as a technology to develop ... Experience interfacing with the FDA, NIH, or other regulatory/health-focused government agencies.
Software Developer Mid-level (II) (ITS12) Custom Computer Programming Services
Silver Spring, MD · On-site
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
Software Developer Mid-level (II) (ITS12) Custom Computer Programming Services
Silver Spring, MD · On-site
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
Subject Manager II (ITS3) Custom Computer Programming Services
Silver Spring, MD · On-site
$119K - $120K/yr
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
Subject Manager II (ITS3) Custom Computer Programming Services
Silver Spring, MD · On-site
$119K - $120K/yr
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
Our FDA-licensed, state-of-the-art CGMP gene therapy campus in Harmans, MD-just minutes from BWI ... Knowledgeable and/or exposure to biological manufacturing processes including microbial and cell ...
Our FDA-licensed, state-of-the-art CGMP gene therapy campus in Harmans, MD-just minutes from BWI ... Knowledgeable and/or exposure to biological manufacturing processes including microbial and cell ...
Test Engineer I (ITS15) Custom Computer Programming Services
Silver Spring, MD · On-site
$114K - $135K/yr
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
Test Engineer I (ITS15) Custom Computer Programming Services
Silver Spring, MD · On-site
$114K - $135K/yr
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
Subject Manager III (ITS4) Custom Computer Programming Services
Silver Spring, MD · On-site
$119K - $120K/yr
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
Subject Manager III (ITS4) Custom Computer Programming Services
Silver Spring, MD · On-site
$119K - $120K/yr
The FDA is seeking Small Business (SB) sources to determine the availability and capability of ... biologics, medical devices, and radiological products. * The scope of this contract is to provide ...
Fda Biologist information
See Silver Spring, MD salary details
$36.4K - $45.4K
6% of jobs
$45.4K - $54.5K
9% of jobs
$59.8K is the 25th percentile. Wages below this are outliers.
$54.5K - $63.5K
17% of jobs
$63.5K - $72.5K
13% of jobs
The median wage is $77.6K / yr.
$72.5K - $81.6K
10% of jobs
$81.6K - $90.6K
7% of jobs
$90.6K - $99.6K
12% of jobs
$103K is the 75th percentile. Wages above this are outliers.
$99.6K - $108.7K
4% of jobs
$108.7K - $117.7K
4% of jobs
$117.7K - $126.7K
1% of jobs
$126.7K - $135.8K
17% of jobs
$36.4K
$88K
$135.8K
How much do fda biologist jobs pay per year?
What are the typical daily responsibilities of an FDA biologist?
An FDA Biologist’s daily tasks often include reviewing scientific data, conducting laboratory experiments, and preparing reports on biological product submissions. You may assess the safety and efficacy of products such as vaccines or medical devices, ensuring compliance with regulatory standards. Collaboration with interdisciplinary teams—including chemists, statisticians, and regulatory affairs specialists—is common to address scientific questions and support regulatory decision-making. The role also involves staying updated on scientific advancements and regulatory changes relevant to the field. This dynamic environment provides opportunities to contribute to public health while developing specialized expertise.
What are the key skills and qualifications needed to thrive in the FDA biologist position, and why are they important?
To thrive as an FDA Biologist, you need a degree in biology or a related scientific field, strong analytical and laboratory skills, and a solid understanding of regulatory requirements. Familiarity with laboratory instruments, scientific data analysis tools, and regulatory databases such as GLP (Good Laboratory Practice) systems is important. Attention to detail, effective communication, and strong problem-solving abilities are valuable soft skills in this role. These competencies are crucial for accurately evaluating biological data, ensuring regulatory compliance, and collaborating effectively within multidisciplinary teams at the FDA.
What is an FDA biologist?
An FDA Biologist is a scientist who evaluates biological products, research data, and laboratory studies to ensure public health and safety. They work on regulatory reviews, inspections, and policy development related to vaccines, gene therapy, blood products, and other biologics. Their role helps ensure compliance with federal regulations and supports scientific advancements in healthcare.

Office Director, Office of Pharmacovigilance and Epidemiology
Silver Spring, MD • On-site
$213K/yr
Other
Posted 24 days ago
Job description
The candidate must meet the following qualifications for this Title 21 position:
- Scientific, Technical, and/or Professional Fields
- Qualified and Outstanding Candidates
b, Outstanding candidates can be defined by existing outstanding work experience, outstanding performance rating, or both.
Technical Qualifications: Candidates do not need to provide narrative responses. However, the technical qualifications must be reflected within the candidate's two-page resume.
- At least 3 years experience in managing a multi-disciplinary professional staff that is responsible for developing and using epidemiologic and other evidence to assess the effectiveness and safety of human drug and therapeutic biologic products and making recommendations on actions to improve patient safety and protect and promote the public health.
- Demonstrated ability in providing authoritative and professional expertise in health sciences, including epidemiology, drug safety and population health issues related to the regulation of human drug and therapeutic biological products to internal and external stakeholders.
- Demonstrated ability in providing critical reviews in the study design and methods of epidemiologic and other study protocols relevant to the assessment of post-marketing drug safety submitted by the pharmaceutical industry.
- Experience applying the Food and Drug Administration Amendments Act, regulations, policies, and procedures related to the regulation and evaluation of drugs and biologic products.
This position is designated as an SES Equivalent position and is covered under the FDA Title 21 Executive Performance Management System and identified as a public filing position for ethics purposes. NOTE: Applicants must submit all relevant transcripts that demonstrate you possess the required education to meet the Basic Qualifications.
Supervisory Responsibilities:
- The incumbent provides occupational specific technical and administrative direction 25 percent or more of the time to three or more subordinate employees performing the work and functions of the organization.
- Obtains resources and identifies strategic objectives for the organization.
- Defines jobs, selects employees, and assigns work; defines technical work requirements and milestones; evaluates the organization and employee accomplishments by accepting or rejecting work products; and presents and defends organization and employees work to senior management and other offices.
- Recommends employee promotions and recognition; approves leave; implements performance modifications and takes corrective actions as appropriate.
- Provides employees with resources and information that ensure a safe and healthy work environment.
- U.S. Citizenship requirement or proof of being a U.S. National must be met by closing date.
- The candidate selected for this position will serve under a career or career-conditional appointment within the competitive service.
- Direct Deposit: You will be required to have all federal salary payments electronically deposited into a bank account with a financial institution of your choice.
- FDA participates in e-Verify: All new hires must complete the I-9 form; this information will be processed through e-Verify to determine your employment eligibility. If a discrepancy arises, you must take affirmative steps to resolve the matter.
- Males born after December 31, 1959, must be registered with the Selective Service. Please go to http://www.sss.gov for more information.
- Background Investigation Requirement: All employees must pass a security investigation. Failing to pass the background check may be grounds for removal or legal action. If hired, you may be subject to additional investigations at a later time.
- Certification of Accuracy: All information concerning eligibility and qualification is subject to investigation and verification. False representation may be grounds for non-consideration, non-selection, or appropriate legal action.
- All applicants tentatively selected for this position will be required to submit to urinalysis to screen for illegal drug use prior to appointment and be subject to random, reasonable suspicion, and post-accident drug testing upon hiring.
- Appointment to the position will be contingent upon a negative applicant drug test result.
- Probationary periods are required for new employees appointed to competitive service positions for the first time; or reinstated employees who return after a break in service of 30-days or more and who have not completed a probationary period.
- Pre-employment physical required: No
- Drug testing required: No
- License required: No
- Mobility agreement required: No
- Immunization required: No
- Bargaining Unit: No
- Telework eligible position: Telework is at the discretion of the supervisor.
- Ethics preclearance/OGE-278, required: Please be advised that this position is subject to FDA's prohibited financial interest regulation and may require the incumbent of this position to divest of certain financial interests. Applicants are advised to seek additional information on this requirement from the hiring official before accepting this position. For more information please visit the FDA Ethics web page: https://www.fda.gov/about-fda/jobs-and-training-fda/ethics.
- Financial disclosure statement, required: This position requires financial disclosure reporting and will be subject to FDA's prohibited financial interest regulation. If you are hired, you may be required to divest of certain financial interests. You are advised to seek additional information on this requirement from the hiring official before accepting any job offers.
- Employment is subject to the successful completion of a background investigation, verification of qualifications, completion of onboarding forms, submission of required documents, and any other job-related requirement before or after appointment.
https://www.opm.gov/policy-data-oversight/classification-qualifications/general-schedule-qualification-standards/0600/general-medical-and-healthcare-series-0601/
Pay careful attention to the Qualifications and Education sections to identify vacancies where a transcript is required. Even if you hold a similar position or are a current employee, you are not exempt from transcript requirements.
TRANSCRIPTS (Required): Positions which are scientific or technical in nature often have very specific educational requirements. You must submit an official transcript, unofficial transcript, or a list including courses, grades earned, completion dates, and quarter and semester hours earned.
Education must be accredited by an accrediting institution recognized by the U.S. Department of Education in order for it to be credited towards qualifications. Therefore, provide only the attendance and/or degrees from schools accredited by accrediting institutions recognized by the U.S. Department of Education.
If you are using education completed in foreign colleges or universities, see the Foreign Education section below for additional requirements.
Electronic Transcript Caution: If you have obtained your transcripts electronically, the file might contain security measures that could prevent our application system from reading the file. Therefore, you should consider asking the institution to provide the file in a non-secured electronic format. Alternatively, you could scan or take a photo of the printed copy of the transcript. If your uploaded transcript cannot be read by our system, you may receive consideration and credit for the information we can access.
Foreign Education: If you are using education completed in foreign colleges or universities to meet the qualification requirements, you must show that the education credentials have been evaluated by a private organization that specializes in interpretation of foreign education programs and such education has been deemed equivalent to that gained in an accredited U.S. education program; or full credit has been given for the courses at a U.S. accredited college or university. For further information, visit the U.S. Department of Education website for Foreign Education Evaluation.
To be acceptable, the foreign credential evaluation must include/describe at a minimum, the following information: (1) The type of education received by the applicant; (2) The level of education in relation to the U.S. education system, and state that its comparability recommendations follow the general guidelines of the International Evaluation Standards Council; (3) The content of the applicant's educational program earned abroad, and the standard obtained; (4) The status of the awarding foreign school's recognition and legitimacy in its home country's education system; and (5) Any other information of interest such as what the evaluation service did to obtain this information, the qualifications of the evaluator, and any indications as to other problems such as forgery.
Note: Some positions require the completion of specific courses or a specified number of credit hours. Therefore, the foreign credential evaluation should provide information similar to that of an official transcript, to include a list of the courses taken, quarter and/or semester hours awarded, the cumulative grade point average (GPA), honors received, if any, date degree awarded.
Applicants can request an evaluation from a member organization of one of the two national associations of credential evaluation services listed below:
- National Association of Credential Evaluation Services (NACES)
- Association of International Credentials Evaluators (AICE)
For more information about this requirement, please visit the U.S. Department of Education website for Foreign Education Evaluation.Employment Type: OTHER