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Fda Inspector Jobs in Dallas, TX (NOW HIRING)

... inspections and audits by agencies such as FDA, EMA, and Notified Bodies. Act as a liaison with regulatory authorities during inspections, responding to queries and providing necessary documentation ...

Maintain compliance with SQF, HACCP, GMP, FDA, FSMA, OSHA, and all customer requirements * Conduct internal audits, GMP inspections, sanitation inspections, and food safety assessments * Lead ...

Maintain compliance with SQF, HACCP, GMP, FDA, FSMA, OSHA, and all customer requirements * Conduct internal audits, GMP inspections, sanitation inspections, and food safety assessments * Lead ...

Showing results 21-40

Fda Inspector information

See Dallas, TX salary details

$24.2K

$54.3K

$97.9K

How much do fda inspector jobs pay per year?

As of Aug 16, 2026, the average yearly pay for fda inspector in Dallas, TX is $54,339.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,100.00 and $62,800.00 per year, depending on experience, location, and employer.

What types of facilities or products do FDA inspectors review, and what does a typical inspection process involve?

FDA Inspectors routinely examine a variety of facilities, such as food processing plants, pharmaceutical manufacturers, medical device companies, and cosmetic production sites, to ensure compliance with federal safety and quality regulations. A typical inspection involves reviewing operational procedures, examining production environments, sampling products, and interviewing staff to identify potential violations or risks. Inspectors often work onsite, sometimes with travel required to cover multiple locations within their region, and collaborate closely with facility management to explain findings and recommend corrective actions. This role offers the opportunity to make a significant impact on public health and provides clear advancement pathways into specialized inspection or supervisory roles within regulatory agencies.

What skills and qualifications are needed to be an FDA inspector?

To thrive as an FDA Inspector, you need a solid background in science or public health, attention to detail, and thorough knowledge of regulatory standards, often supported by a relevant degree. Familiarity with inspection protocols, laboratory testing equipment, and digital reporting systems is commonly required, along with potential USDA or FDA certifications. Strong analytical thinking, effective communication, and integrity are important soft skills for this role. These competencies ensure accurate inspections, compliance with safety regulations, and clear reporting essential to public health and organizational accountability.

How do you become an FDA inspector?

To become an FDA inspector, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or food science, along with experience in food safety, pharmaceuticals, or related areas. They must pass the FDA's specialized training program and often require a background check and security clearance; some positions may also require state licensure or certifications. Strong attention to detail, knowledge of regulatory standards, and good communication skills are essential for the role.

What does an FDA inspector do?

An FDA Inspector is responsible for ensuring that companies comply with federal regulations related to food, drugs, medical devices, and other products overseen by the U.S. Food and Drug Administration. They conduct inspections, review records, collect samples, and assess manufacturing practices to ensure public health and safety. Inspectors may also investigate complaints, issue compliance notices, and recommend enforcement actions if violations are found.

What are popular job titles related to Fda Inspector jobs in Dallas, TX?

For Fda Inspector jobs in Dallas, TX, the most frequently searched job titles are:

What cities near Dallas, TX are hiring for Fda Inspector jobs?

Cities near Dallas, TX with the most Fda Inspector job openings:

Infographic showing various Fda Inspector job openings in Dallas, TX as of August 2026, with employment types broken down into 70% Full Time, and 30% Contract. Highlights an 100% In-person job distribution, with an average salary of $54,339 per year, or $26.1 per hour.

QA/RA Specialist - Pharmaceutical GLP/GMP Experience

synergy

Dallas, TX

Full-time

Medical, Dental, Vision, PTO

Re-posted 24 days ago


Job description

QA/RA Specialist - Pharmaceutical GLP/GMP Experience

Synergy is seeking a knowledgeable and meticulous QA/RA Specialist with strong expertise in Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) within the pharmaceutical industry. The specialist will be responsible for supporting the implementation, maintenance, and continuous improvement of quality and regulatory compliance systems to ensure adherence to FDA, EMA, and other regulatory requirements. This role involves reviewing procedures, ensuring documentation compliance, conducting internal audits, and assisting with regulatory submissions and inspections.

Key Responsibilities:

  • Develop, review, and maintain quality assurance and regulatory affairs documentation in compliance with GLP and GMP standards.
  • 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 standards.
  • Support preparation and management of regulatory submissions and responses to regulatory agencies.
  • Collaborate with cross-functional teams to ensure compliance throughout product lifecycle.
  • Assist in training laboratory and manufacturing staff on quality system requirements and regulatory standards.
  • Investigate and support resolution of deviations, non-conformances, and CAPA activities.

Education & Experience:

  • Bachelor's degree in life sciences, pharmacy, chemistry, or related field.
  • Minimum 5 years of experience in pharmaceutical GLP/GMP quality assurance and regulatory affairs.
  • Strong knowledge of FDA, EMA regulations, and ICH guidelines.
  • Experience with internal auditing and regulatory inspections.

Requirements

Education:

  • Bachelor's degree in life sciences, pharmacy, chemistry, or a related discipline.

Experience:

  • At least 5 years of hands-on experience in pharmaceutical GLP/GMP QA and regulatory affairs.
  • Familiarity with international regulatory frameworks including FDA, EMA, and ICH guidelines.
  • Proven experience conducting internal audits and supporting regulatory inspections.

Skills:

  • Strong attention to detail and organizational skills.
  • Excellent communication and interpersonal abilities.
  • Ability to work collaboratively with cross-functional teams and manage multiple priorities.
  • Proficiency in quality management systems and documentation practices.

Benefits

  • Health Care Plan (Medical, Dental & Vision)
  • Paid Time Off (Vacation, Sick & Public Holidays)
  • Training & Development