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Us Fda Jobs in Texas (NOW HIRING)

PET Facility Manager

Austin, TX · On-site

$100K - $125K/yr

Experience with HPLC, radiochemistry synthesis, US FDA cGMP, Radiation Safety Principles, Isotopes production and analytical equipment troubleshooting and maintenance a plus. * Superior teamwork ...

Head of US Engineering

Houston, TX · On-site

$180 - $260/hr

You will lead the US engineering team and, with the Head of UKEngineering, maintain one common ... Lead representative at regulatory, certification andcustomer audits and inspections, including FDA ...

Understanding of clinical trials, including US-FDA 510(k) / PMA regulatory pathway * Knowledge of routine assessments made from spine and/or orthopedic imaging exams * History of collaboration with ...

Understanding of clinical trials, including US-FDA 510(k) / PMA regulatory pathway * Knowledge of routine assessments made from spine and/or orthopedic imaging exams * History of collaboration with ...

Join us at MMS and be part of a team that is shaping the future of clinical research. Discover more ... Strong knowledge of CDISC (especially SDTM and ADaM), looks to understand guidance from FDA from ...

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Us Fda information

See Texas salary details

$8

$33

$69

How much do us fda jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for us fda in Texas is $33.80, according to ZipRecruiter salary data. Most workers in this role earn between $19.45 and $43.55 per hour, depending on experience, location, and employer.

What is the US FDA?

The US FDA, or United States Food and Drug Administration, is a federal agency responsible for protecting public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, food supply, cosmetics, and products that emit radiation. The FDA regulates and oversees the approval of new drugs and medical devices, monitors food safety, and enforces regulations to ensure products meet safety standards. The agency also provides guidance to industry and the public on issues related to health and safety.

What are the key skills and qualifications needed to thrive as a US FDA Regulatory Affairs Specialist?

To thrive as a US FDA Regulatory Affairs Specialist, you need in-depth knowledge of FDA regulations, strong analytical skills, and a degree in life sciences or a related field. Familiarity with regulatory submission platforms like eCTD, and certifications such as RAC (Regulatory Affairs Certification), are highly valuable. Exceptional attention to detail, problem-solving abilities, and strong written and verbal communication skills help professionals excel in this role. These skills ensure compliance with complex regulations, effective communication with regulatory agencies, and successful product approvals.

What are some common challenges faced by professionals working in roles related to the US FDA?

Professionals working in roles related to the US FDA often encounter challenges such as staying updated with frequently changing regulations and ensuring strict compliance with all applicable guidelines. They may also face tight deadlines when preparing documentation for product submissions or responding to regulatory inquiries. Collaboration across multidisciplinary teams—including legal, scientific, and quality assurance departments—is essential, which can require strong communication and project management skills. Navigating complex processes and balancing regulatory requirements with business needs are key aspects of the role.

What is the difference between Us Fda vs Us Pharmacist?

AspectUs FdaUs Pharmacist
Required CredentialsRegulatory knowledge, possibly a degree in health sciencesDoctor of Pharmacy (PharmD), state licensure
Work EnvironmentRegulatory agencies, laboratories, compliance officesPharmacies, hospitals, clinics
Industry UsageRegulatory oversight, policy developmentPatient care, medication dispensing
Common Search/ComparisonRegulatory roles, compliance jobsClinical roles, medication management

The main difference is that Us Fda professionals focus on regulation, compliance, and policy within the healthcare industry, often working for government agencies. In contrast, Us Pharmacists are healthcare providers directly involved in patient care and medication dispensing. While both roles require healthcare knowledge, their work environments and responsibilities differ significantly.

What qualifications do I need for US FDA jobs?

US FDA jobs typically require a bachelor's degree in a relevant field such as science, engineering, or healthcare, along with relevant work experience. Some positions may require advanced degrees or professional certifications, and strong analytical, communication, and regulatory knowledge are often essential. Specific qualifications vary depending on the role and level of responsibility.

What are popular job titles related to Us Fda jobs in Texas?

For Us Fda jobs in Texas, the most frequently searched job titles are:

What cities in Texas are hiring for Us Fda jobs?

Cities in Texas with the most Us Fda job openings:

Infographic showing various Us Fda job openings in Texas as of August 2026, with employment types broken down into 83% Full Time, 9% Part Time, and 8% Contract. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $70,304 per year, or $33.8 per hour.

POSTDOCTORAL RESEARCHER - Radiology - Nuclear Medicine - Sun Lab [Req#: 886058, Position#: 126365]

Dallas, TX • On-site


UT Southwestern Medical Center
Hospitals • 10K+ employees

7.9

Company rating: 7.9 out of 10

Based on 152 frontline employees who took The Breakroom Quiz

106th of 895 rated healthcare providers

People enjoy working here

Good employer

Recommended by students


Full-time

Re-posted 13 days ago


Job description

Description
The Department of Radiology at the University of Texas Southwestern Medical Center (UT Southwestern, Dallas, Texas) is looking for highly motivated synthetic chemists to work on various projects with research focus on the design, synthesis, and biological evaluations of targeted imaging probes or theranostic agents for noninvasive disease detection and therapy assessment.
Major research resources available include a recently established state-of-the-art Cyclotron and Radiochemistry Program (CRP) (http://www.utsouthwestern.edu/research/cyclotron/index.html) and a Small Animal Imaging Shared Resource (SAISR) funded by an NCI Cancer Center Support Grant (https://www.utsouthwestern.edu/departments/simmons/research/shared-resources/).
Equipped with a GE PETtrace 880 cyclotron and a Current Good Manufacturing Practice (CGMP) Radiopharmacy, the CRP produces PET radiotracers as needed on fourteen (14) US-FDA Investigational New Drug (IND) and one (1) Abbreviated New Drug Application (ANDA) approvals for clinical PET practice and research, in addition to over fifty (50) preclinical radiotracers for studies in various diseased animal models. With a comprehensive set of preclinical animal imaging modalities, the SAISR enables noninvasive assessment of anatomy, pathophysiology, molecular targets, pharmacodynamics, pharmacokinetics, and dosimetry.
Qualifications
Candidates must hold a recent Ph.D. and/or M.D. degree. Experience with small animal imaging, medical radioisotopes, and live animlas is desired but not required.
Application Instructions
Interested individuals must upload a CV, cover letter, and a list of three references.


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