Stay updated on FDA/CFR regulations and train staff accordingly.
Quick apply
Stay updated on FDA/CFR regulations and train staff accordingly.
Director of Engineering
Dallas, TX · On-site
PJI currently lacks FDA-approved therapies and forces patients through grueling, months-long treatments with poor outcomes. Our disruptive technology transforms this journey by safely delivering high ...
Director of Engineering
Dallas, TX · On-site
PJI currently lacks FDA-approved therapies and forces patients through grueling, months-long treatments with poor outcomes. Our disruptive technology transforms this journey by safely delivering high ...
Director of Engineering
Dallas, TX · On-site
PJI currently lacks FDA-approved therapies and forces patients through grueling, months-long treatments with poor outcomes. Our disruptive technology transforms this journey by safely delivering high ...
Director of Engineering
Dallas, TX · On-site
PJI currently lacks FDA-approved therapies and forces patients through grueling, months-long treatments with poor outcomes. Our disruptive technology transforms this journey by safely delivering high ...
Cybersecurity Engineer
Dallas, TX · On-site
Execute and document risk evaluation aligned with AAMI TIR57, AAMI TIR97, FDA Premarket Cybersecurity Guidance, and ISO 14971. * Participate actively in Coordinated Vulnerability Disclosure (CVD ...
Quick apply
Cybersecurity Engineer
Dallas, TX · On-site
Execute and document risk evaluation aligned with AAMI TIR57, AAMI TIR97, FDA Premarket Cybersecurity Guidance, and ISO 14971. * Participate actively in Coordinated Vulnerability Disclosure (CVD ...
Performs internal departmental audits and supports audits by third parties e.g., BSI, FDA and others, as required Initiates and maintains required establishment listings e.g., FDA and EU, including ...
Performs internal departmental audits and supports audits by third parties e.g., BSI, FDA and others, as required Initiates and maintains required establishment listings e.g., FDA and EU, including ...
Performs internal departmental audits and supports audits by third parties e.g., BSI, FDA and others, as required. * Initiates and maintains required establishment listings e.g., FDA and EU ...
Performs internal departmental audits and supports audits by third parties e.g., BSI, FDA and others, as required. * Initiates and maintains required establishment listings e.g., FDA and EU ...
Performs internal departmental audits and supports audits by third parties e.g., BSI, FDA and others, as required. * Initiates and maintains required establishment listings e.g., FDA and EU ...
Performs internal departmental audits and supports audits by third parties e.g., BSI, FDA and others, as required. * Initiates and maintains required establishment listings e.g., FDA and EU ...
PJI currently lacks FDA-approved therapies and forces patients through grueling, months-long treatments with poor outcomes. Our disruptive technology transforms this journey by safely delivering high ...
Quick apply
PJI currently lacks FDA-approved therapies and forces patients through grueling, months-long treatments with poor outcomes. Our disruptive technology transforms this journey by safely delivering high ...
Ensure adherence to regulatory requirements from FDA, EMA, and other global regulatory agencies. * Conduct internal audits and inspections to assess compliance with quality systems and regulatory ...
Ensure adherence to regulatory requirements from FDA, EMA, and other global regulatory agencies. * Conduct internal audits and inspections to assess compliance with quality systems and regulatory ...
Director of Engineering
Dallas, TX · On-site
$200 - $225/hr
PJI currently lacks FDA-approved therapies and forces patients through grueling, months-long treatments with poor outcomes. Our disruptive technology transforms this journey by safely delivering high ...
Director of Engineering
Dallas, TX · On-site
$200 - $225/hr
PJI currently lacks FDA-approved therapies and forces patients through grueling, months-long treatments with poor outcomes. Our disruptive technology transforms this journey by safely delivering high ...
Senior Quality Engineer, Cybersecurity
Dallas, TX · On-site
$87K - $118K/yr
Supports integration of ISO 14971 risk management, IEC 62366 usability engineering, and FDA cybersecurity guidance into SDLC processes, ensuring a cohesive and compliant approach to product safety ...
Senior Quality Engineer, Cybersecurity
Dallas, TX · On-site
$87K - $118K/yr
Supports integration of ISO 14971 risk management, IEC 62366 usability engineering, and FDA cybersecurity guidance into SDLC processes, ensuring a cohesive and compliant approach to product safety ...
Food Safety Manager
Alvarado, TX · On-site
$13 - $16/hr
Ensure adherence to FDA and produce safety guidelines. * Monitor food safety practices related to produce handling. * Stay up to date on food safety regulations and requirements. Qualifications:
Quick apply
Food Safety Manager
Alvarado, TX · On-site
$13 - $16/hr
Ensure adherence to FDA and produce safety guidelines. * Monitor food safety practices related to produce handling. * Stay up to date on food safety regulations and requirements. Qualifications:
Develop and implement regulatory strategies for medical devices, ensuring compliance with global regulations (FDA, EU MDR, Health Canada, TGA, etc.). Advise on the appropriate regulatory pathways (e ...
Develop and implement regulatory strategies for medical devices, ensuring compliance with global regulations (FDA, EU MDR, Health Canada, TGA, etc.). Advise on the appropriate regulatory pathways (e ...
Develop and implement regulatory strategies for medical devices, ensuring compliance with global regulations (FDA, EU MDR, Health Canada, TGA, etc.). Advise on the appropriate regulatory pathways (e ...
Develop and implement regulatory strategies for medical devices, ensuring compliance with global regulations (FDA, EU MDR, Health Canada, TGA, etc.). Advise on the appropriate regulatory pathways (e ...
Develop and implement regulatory strategies for medical devices, ensuring compliance with global regulations (FDA, EU MDR, Health Canada, TGA, etc.). Advise on the appropriate regulatory pathways (e ...
Develop and implement regulatory strategies for medical devices, ensuring compliance with global regulations (FDA, EU MDR, Health Canada, TGA, etc.). Advise on the appropriate regulatory pathways (e ...
Warehouse Lead
Burleson, TX · On-site
$16 - $20.50/hr
Train and mentor warehouse staff on SOPs, FDA/GMP requirements, inventory practices, and warehouse safety standards * Receive inbound shipments of finished goods, components, and materials and verify ...
Quick apply
Warehouse Lead
Burleson, TX · On-site
$16 - $20.50/hr
Train and mentor warehouse staff on SOPs, FDA/GMP requirements, inventory practices, and warehouse safety standards * Receive inbound shipments of finished goods, components, and materials and verify ...
Be Seen First
Clinical Research Coordinator (CRC)
Flower Mound, TX · On-site
$50K - $70K/yr
Ensure strict adherence to GCP, FDA regulations, and protocol requirements * Maintain high-quality source documentation and EDC data entry (real-time, audit-ready) * Manage investigational product ...
Quick apply
Be Seen First
Clinical Research Coordinator (CRC)
Flower Mound, TX · On-site
$50K - $70K/yr
Ensure strict adherence to GCP, FDA regulations, and protocol requirements * Maintain high-quality source documentation and EDC data entry (real-time, audit-ready) * Manage investigational product ...
FDA, ISO, etc.) and actively participate and represent the company in 3rd party inspections. Maintain up-to-date knowledge, identify, and monitor applicable standards and guidance documents for ...
FDA, ISO, etc.) and actively participate and represent the company in 3rd party inspections. Maintain up-to-date knowledge, identify, and monitor applicable standards and guidance documents for ...
ROC Medical Release Clerk
Irving, TX · On-site
The primary responsibility is to review product release paperwork for Matheson locations all over the country to fulfill the requirements of the FDA. This position works closely with local operations ...
ROC Medical Release Clerk
Irving, TX · On-site
The primary responsibility is to review product release paperwork for Matheson locations all over the country to fulfill the requirements of the FDA. This position works closely with local operations ...
ROC Medical Release Clerk
Irving, TX · On-site
The primary responsibility is to review product release paperwork for Matheson locations all over the country to fulfill the requirements of the FDA. This position works closely with local operations ...
ROC Medical Release Clerk
Irving, TX · On-site
The primary responsibility is to review product release paperwork for Matheson locations all over the country to fulfill the requirements of the FDA. This position works closely with local operations ...
Fda information
See Dallas, TX salary details
$13.28 - $18.98
11% of jobs
$23.58 is the 25th percentile. Wages below this are outliers.
$18.98 - $24.67
18% of jobs
$24.67 - $30.36
16% of jobs
The median wage is $33.21 / hr.
$30.36 - $36.06
12% of jobs
$36.06 - $41.75
11% of jobs
$46.02 is the 75th percentile. Wages above this are outliers.
$41.75 - $47.44
12% of jobs
$47.44 - $53.13
9% of jobs
$53.13 - $58.83
5% of jobs
$58.83 - $64.52
3% of jobs
$64.52 - $70.21
2% of jobs
$70.21 - $75.91
2% of jobs
$13
$38
$75
How much do fda jobs pay per hour?
As of Aug 23, 2026, the average hourly pay for fda in Dallas, TX is $38.83, according to ZipRecruiter salary data. Most workers in this role earn between $24.19 and $48.39 per hour, depending on experience, location, and employer.
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?
| Aspect | Fda | Food Scientist |
|---|---|---|
| Required Credentials | Typically a degree in health, science, or related field; certifications vary | Bachelor's or master's in food science, microbiology, or related |
| Work Environment | Regulatory agencies, laboratories, inspection sites | Food manufacturing facilities, laboratories, research settings |
| Employer & Industry Usage | U.S. Food and Drug Administration, government agencies | Food companies, research institutions, government agencies |
| Common Search & Comparison Intent | Understanding regulatory roles, compliance, and enforcement | Food 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 Dallas, TX?
The most popular types of Fda jobs in Dallas, TX are:
What are popular job titles related to Fda jobs in Dallas, TX?
For Fda jobs in Dallas, TX, the most frequently searched job titles are:
What job categories do people searching Fda jobs in Dallas, TX look for?
The top searched job categories for Fda jobs in Dallas, TX are:
What cities near Dallas, TX are hiring for Fda jobs?
Cities near Dallas, TX with the most Fda job openings:
Job description
Job Title: Quality Assurance Supervisor
Job Location: Midlothian, TX
Job Type: Full Time
Job Description:
Supervise, train, and motivate QA personnel; enforce company policies.
Review and audit production, QC, and sanitation records; ensure GMP and FDA compliance.
Lead investigations (OOS, CAPA, deviations, complaints, NCMR).
Maintain QA documentation at audit-ready standards.
Conduct monthly GMP audits and oversee supplier qualification records.
Manage QMS programs (GMP, HACCP, Sanitation, Allergen, Pest Control, etc.).
Coordinate with production and inventory teams on reworks and quality issues.
Support regulatory audits (FDA, NSF, Kosher, Halal, etc.).
Ensure calibration and maintenance of quality instruments.
Stay updated on FDA/CFR regulations and train staff accordingly.
About Staffingine
Sourced by ZipRecruiter
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Atlanta, GA, US
Year founded
2016