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Fda Jobs in Texas (NOW HIRING)

Bimeda Inc.

Regulatory Affairs Associate

Houston, TX

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Maintain awareness of evolving FDA and industry requirements through ongoing review of regulations, * guidance documents, and industry publications. * Cross-functional communication and data ...

Neurology Rare Disease Center

Be Seen First

Clinical Research Coordinator (CRC)

Flower Mound, TX · On-site

$50K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

Consumer Capital Management LLC

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 ...

Houston Methodist

This position communicates with regulatory affairs office for FDA submissions across multiple studies of different therapeutic areas and phases in accordance with appropriate regulations, Standard ...

Bimeda Inc.

Regulatory Affairs Associate

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Maintain awareness of evolving FDA and industry requirements through ongoing review of regulations, * guidance documents, and industry publications. * Cross-functional communication and data ...

Stark Pharma Solutions Inc

CQV Engineer

Austin, TX · On-site

Ensure compliance with GMP, FDA regulations, cGMP guidelines, and internal quality management systems. * Analyze validation data, investigate deviations, support root cause analysis, and implement ...

krg technology inc

Senior Project Manager

Waco, TX · On-site

Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements. Project Management / Planning practices, principles, tools and techniques.

Confidential

Quality Assurance Engineer IV

Seguin, TX

$85K - $99K/yr

This position will be responsible for maintaining compliance with SQF, HACCP, GMP, and FDA food-contact requirements while providing hands-on technical support to manufacturing operations. The ideal ...

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How much do fda jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for fda in Texas is $34.60, according to ZipRecruiter salary data. Most workers in this role earn between $21.56 and $43.13 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?

AspectFdaFood Scientist
Required CredentialsTypically a degree in health, science, or related field; certifications varyBachelor's or master's in food science, microbiology, or related
Work EnvironmentRegulatory agencies, laboratories, inspection sitesFood manufacturing facilities, laboratories, research settings
Employer & Industry UsageU.S. Food and Drug Administration, government agenciesFood companies, research institutions, government agencies
Common Search & Comparison IntentUnderstanding regulatory roles, compliance, and enforcementFood 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 healthcare. Many positions require specialized knowledge, experience, or advanced degrees, and some roles may require professional certifications or licenses. Strong analytical skills, attention to detail, and familiarity with regulatory guidelines are also important.

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

The most popular types of Fda jobs in Texas are:

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

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

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

The top searched job categories for Fda jobs in Texas are:

What cities in Texas are hiring for Fda jobs?

Cities in Texas with the most Fda job openings:

Fda jobs near you
Infographic showing various Fda job openings in Texas as of August 2026, with employment types broken down into 90% Full Time, 5% Part Time, and 5% Contract. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $71,976 per year, or $34.6 per hour.

Quality Engineer--Manufacturng

Diversified Sourcing Solutions

Waco, TX

$90K/yr

Full-time

Re-posted 12 days ago

Job description

POSITION SUMMARY
The Quality Engineer is responsible for ensuring compliance, safety, and quality of beverage products manufactured under Low-Acid Canned Food (LACF) regulations using thermal processing (retort). This role supports process validation, regulatory compliance, quality systems, and continuous improvement initiatives to guarantee product safety and adherence to FDA, HACCP, and applicable food safety standards. The Quality Engineer will report to the Quality Manager. This position will work with sensitive information; therefore, it will require an NDA.

KEY RESPONSIBILITIES
  • Ensure compliance with FDA LACF regulations (21 CFR Part 113) and related food safety requirements.
  • Maintain and support Scheduled Process filings (FDA Form 2541) in coordination with Process Authorities.
  • Verify adherence to thermal process parameters (time, temperature, pressure, venting, come-up time).
  • Support and maintain compliance with HACCP, Preventive Controls (FSMA), and GMPs.
  • Act as a subject matter expert for retort processing compliance and deviation handling.
  • Monitor and validate retort operations, this will include Temperature distribution (TD), heat penetration (HP) studies, Venting and air removal verification, and Critical factor control operations. 7. Investigate and document process deviations, including thermal process deviations, and lead corrective actions.
  • Collaborate with Process Authorities to establish and optimize scheduled processes.
  • Ensure calibration and proper functioning of critical instruments (temperature probes, pressure gauges, recorders).
  • Develop, implement, and maintain SOPs, work instructions, and quality documentation.
  • Perform internal audits and support third-party or regulatory inspections.
  • Maintain records per LACF requirements (retort logs, deviation logs, calibration records).
  • Lead or participate in root cause analysis (RCA) and CAPA processes.
  • Lead validation activities for new products, processes, or equipment related to retort systems.
  • Analyze process data and recommend improvements to enhance product quality, safety, and efficiency.
  • Support continuous improvement initiatives (Lean, Six Sigma, OEE improvements).
  • Implement statistical analysis methods to improve process capability and consistency.
  • Train operations and quality personnel on LACF requirements, retort procedures, critical limits, and Food safety and quality standards.
  • Provide technical support to production, R&D, and maintenance teams.
  • Participate in product development to ensure processes meet regulatory and safety requirements

JOB EFFICIENCY MEASURES
Job performance will be assessed using measurable metrics, which may include but are not limited to:
  • Production output and throughput targets.
  • Accuracy and quality rates.
  • Adherence to safety, regulatory, and compliance standards.
  • Equipment uptime, utilization, and operational efficiency.
  • On-time completion and schedule adherence.
  • Participation in and contribution to continuous improvement initiatives.


QUALIFICATIONS
  • Bachelor’s degree in Food Science, Chemical Engineering, Microbiology, or related field required.
  • Three to Five (3-5) years of experience in food or beverage manufacturing required, with knowledge preferably in LACF / acidified foods and Retort Processing.
  • Experience working with FDA regulations and audits is strongly preferred.
  • Certifications in BPCS, PCQI, and Six Sigma strongly preferred.
  • Fluency in English is a must, Spanish a plus.

Compensation - $90K +

Company Description

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