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Fda Inspector Jobs in Houston, TX (NOW HIRING)

Lonza

Validation Engineer

Houston, TX · On-site

... e.g., FDA, EMA) and industry best practices. * Coordinate validation activities with cross ... Support regulatory inspections and internal audits by providing validation documentation and ...

Lincare

Delivery Driver - Medical Equipment

Conroe, TX

$15 - $18.50/hr

Inspect and maintain company-provided delivery vehicle, ensuring safety during the loading and ... Maintain cleanliness and organization of delivery vehicle and warehouse, adhering to all FDA ...

LGM Pharma, LLC

R&D TECHNICIAN

Rosenberg, TX · On-site

Perform visual inspection and physical testing on intermediates and finished trial products ... Ability to read and interpret technical procedures, SOPs, GMPs, and FDA regulations. * Ability to ...

Lonza

Quality Site Head

Houston, TX · On-site

... FDA, EMA and other regulatory body regulations and guidelines * Serve as the point person with ... Oversee all partner and regulatory authority audits and inspections and corrective action programs

LivaNova

Director - Product Security

Houston, TX · On-site +1

$222K - $233K/yr

Act as the senior product security subject matter expert, representing the company during FDA and other international regulatory inspections. * Post-Market Surveillance & Incident Response: * Oversee ...

Lonza

Quality Site Head

Houston, TX · On-site

... FDA, EMA and other regulatory body regulations and guidelines * Serve as the point person with ... Oversee all partner and regulatory authority audits and inspections and corrective action programs

Imperial Star Solar

Quality Supervisor

Tomball, TX · On-site

$65K - $80K/yr

This position is responsible for overseeing quality control activities, managing inspection teams ... Familiarity with regulatory standards relevant to the industry, such as FDA, ISO/TS, or GMP.

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Fda Inspector information

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$23.4K

$52.5K

$94.5K

How much do fda inspector jobs pay per year?

As of Jul 1, 2026, the average yearly pay for fda inspector in Houston, TX is $52,465.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,800.00 and $60,600.00 per year, depending on experience, location, and employer.

How much do FDA drug investigators make?

FDA drug investigators typically earn a salary ranging from $70,000 to $120,000 annually, depending on experience, location, and level of responsibility. They often hold a bachelor's degree in a relevant field and may require specialized training or certifications related to regulatory compliance and inspection procedures.

What types of facilities or products do FDA Inspectors typically 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 are the key skills and qualifications needed to thrive in the Fda Inspector position, and why are they important?

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.

What type of inspector gets paid the most?

Among FDA inspectors, senior or specialized inspectors, such as those overseeing complex manufacturing facilities or with advanced certifications, tend to earn higher salaries. Experience, certifications, and geographic location also influence pay levels for FDA inspectors. Generally, inspectors with specialized skills or leadership roles earn the most in this field.

Is it hard to get a job at FDA?

Becoming an FDA inspector can be competitive due to strict qualification requirements, including relevant experience, education, and passing civil service exams. Candidates often need a background in science, public health, or regulatory compliance, along with strong attention to detail and communication skills. The hiring process can be lengthy and involves multiple steps such as interviews and background checks.

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 manufacturing. They must pass a written exam and a background check, and often complete on-the-job training or specialized FDA training programs. Certification or licensing is not required but can enhance prospects.

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 the most commonly searched types of Fda Inspector jobs in Houston, TX? The most popular types of Fda Inspector jobs in Houston, TX are:
What are popular job titles related to Fda Inspector jobs in Houston, TX? For Fda Inspector jobs in Houston, TX, the most frequently searched job titles are:
What job categories do people searching Fda Inspector jobs in Houston, TX look for? The top searched job categories for Fda Inspector jobs in Houston, TX are:
What cities near Houston, TX are hiring for Fda Inspector jobs? Cities near Houston, TX with the most Fda Inspector job openings:
Fda Inspector jobs near you
Infographic showing various Fda Inspector job openings in Houston, TX as of June 2026, with employment types broken down into 69% Full Time, 8% Part Time, and 23% Contract. Highlights an 100% In-person job distribution, with an average salary of $52,465 per year, or $25.2 per hour.
Validation Engineer

Validation Engineer

Lonza

Houston, TX • On-site

Full-time

Posted 6 days ago

Lonza rating

8.2

Company rating: 8.2 out of 10

Based on 41 frontline employees who took The Breakroom Quiz

29th of 73 rated pharmaceutical

Job description

Validation Engineer
Houston, TX
The actual location of this job is in Houston, TX, US. Relocation assistance is available for eligible candidates and their families, if needed.
This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
This is an office-first role. Working together in person supports close, real-time collaboration and team alignment, enabling us to deliver our best work. You will work primarily in the office, with the flexibility to work remotely for 20% of your time (one day per week).
What you will get:
  • An agile career and dynamic working culture.
  • An inclusive and ethical workplace.
  • Compensation programs that recognize high performance.
  • A variety of benefits dependent on role and location.

The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits.
What you will do:
  • Develop and execute validation protocols and reports for equipment, utilities, facilities. (e.g., IQ, OQ, PQ).
  • Develop and execute CQV deliverables for Sterilization program. Experience in autoclave cycle development, load development and qualification.
  • Perform risk assessments and develop validation strategies based on regulatory guidelines (e.g., FDA, EMA) and industry best practices.
  • Coordinate validation activities with cross-functional teams including Manufacturing, Quality Assurance, Engineering, and R&D.
  • Analyze validation data, identify deviations, and recommend corrective and preventive actions (CAPAs).
  • Prepare and present validation summaries and reports to internal and external auditors.
  • Participate in the review and approval of change controls related to validated systems.
  • Maintain validation plans and schedules to ensure timely completion of validation activities.
  • Support regulatory inspections and internal audits by providing validation documentation and expertise.
  • Contribute to the continuous improvement of validation processes and procedures.

What we are looking for:
  • Bachelor's degree in Engineering (Chemical, Biomedical, Mechanical, or equivalent) or a related scientific discipline.
  • Minimum of 3-5 years of experience in validation within the biopharmaceutical or pharmaceutical industry.
  • In-depth knowledge of cGMP, ICH guidelines, FDA regulations (21 CFR Parts 210, 211, 820), and other relevant regulatory requirements.
  • Ideal candidates will have hands-on experience in autoclave validation and familiarity with FDA and cGMP standards. Proven experience with IQ, OQ, PQ.
  • Strong understanding of quality systems (e.g., change control, deviations, CAPA).
  • Excellent technical writing and communication skills.
  • Ability to work independently and collaboratively in a fast-paced environment.

About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.

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