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Pharmaceutical Validation Engineer Jobs in Texas

Required * BS in Engineering (Chemical preferred), life sciences or related field. * 3+ years of validation work experience in a pharmaceutical and/or medical device industry. * Certified Quality ...

Required * BS in Engineering (Chemical preferred), life sciences or related field. * 3+ years of validation work experience in a pharmaceutical and/or medical device industry. * Certified Quality ...

Validation engineering in pharmaceutical, biotechnology, or related industry. * Creating validation protocols, deviations, and validation summary reports; utilizing Validation Life Cycle Concept

Validation engineering in pharmaceutical, biotechnology, or related industry. * Creating validation protocols, deviations, and validation summary reports; utilizing Validation Life Cycle Concept

Validation engineering in pharmaceutical, biotechnology, or related industry. * Creating validation protocols, deviations, and validation summary reports; utilizing Validation Life Cycle Concept

Validation engineering in pharmaceutical, biotechnology, or related industry. * Creating validation protocols, deviations, and validation summary reports; utilizing Validation Life Cycle Concept

The Validation Engineer II will build and execute a periodic review program for our validated ... Education in Biotechnology or a related major preferred * 5+ years experience in the pharmaceutical ...

The Validation Engineer II will build and execute a periodic review program for our validated ... Education in Biotechnology or a related major preferred * 5+ years experience in the pharmaceutical ...

Validation Engineer II

Houston, TX · On-site

$85 - $120/hr

The Validation Engineer II will build and execute a periodic review program for our validated ... Education in Biotechnology or a related major preferred5+ years experience in the pharmaceutical or ...

... pharmaceutical manufacturing. We're proud to be recognized as one of Houston's fastest-growing ... POSITION SUMMARY Validation Engineer II drives compliance and manufacturing readiness across ...

... pharmaceutical manufacturing. We're proud to be recognized as one of Houston's fastest-growing ... Position Summary: Validation Engineer II drives compliance and manufacturing readiness across ...

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Pharmaceutical Validation Engineer information

See Texas salary details

$21

$48

$72

How much do pharmaceutical validation engineer jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for pharmaceutical validation engineer in Texas is $48.44, according to ZipRecruiter salary data. Most workers in this role earn between $36.73 and $58.89 per hour, depending on experience, location, and employer.

What does a pharmaceutical validation engineer do?

A Pharmaceutical Validation Engineer is responsible for ensuring that pharmaceutical manufacturing processes, equipment, and systems operate consistently and produce products that meet strict industry standards and regulatory requirements. They design, conduct, and document validation protocols for equipment, processes, and computer systems to confirm their accuracy and reliability. Their work is crucial for maintaining product quality, patient safety, and compliance with agencies such as the FDA and EMA.

What are the key skills and qualifications needed to thrive as a pharmaceutical validation engineer?

Pharmaceutical Validation Engineers need a solid background in engineering or life sciences, with knowledge of regulatory standards such as GMP and experience in validation protocols. Familiarity with technical tools like data loggers, validation software, and documentation systems, as well as certifications like Six Sigma or CQE, are commonly required. Excellent problem-solving, project management, and communication skills help them collaborate across departments and address compliance challenges. These skills and qualifications are crucial to ensure pharmaceutical processes meet regulatory requirements and maintain product quality and patient safety.

What are the most common challenges a pharmaceutical validation engineer faces when working on new equipment qualification projects?

Pharmaceutical Validation Engineers often encounter challenges such as tight project deadlines, managing complex documentation requirements, and ensuring compliance with stringent regulatory standards like FDA or EMA guidelines. Coordinating with cross-functional teams—including production, quality assurance, and maintenance—can also present hurdles, especially when integrating new equipment into existing processes. Proactive communication, strong organizational skills, and a thorough understanding of validation protocols are essential for overcoming these challenges and ensuring successful project outcomes.

What is the difference between Pharmaceutical Validation Engineer vs Quality Assurance Specialist?

AspectPharmaceutical Validation EngineerQuality Assurance Specialist
CertificationsGMP, Validation certificationsGMP, QA certifications
Work EnvironmentValidation labs, manufacturing plantsQuality control labs, production facilities
Primary FocusValidating equipment, processes, systemsEnsuring product quality, compliance
Industry UsageCommon in manufacturing and validation teamsWidespread across quality departments

While both roles work within the pharmaceutical industry and require GMP knowledge, the Pharmaceutical Validation Engineer primarily focuses on validating equipment and processes to ensure compliance, whereas the Quality Assurance Specialist concentrates on maintaining overall product quality and regulatory adherence.

What are popular job titles related to Pharmaceutical Validation Engineer jobs in Texas?

For Pharmaceutical Validation Engineer jobs in Texas, the most frequently searched job titles are:

What cities in Texas are hiring for Pharmaceutical Validation Engineer jobs?

Cities in Texas with the most Pharmaceutical Validation Engineer job openings:

Infographic showing various Pharmaceutical Validation Engineer job openings in Texas as of August 2026, with employment types broken down into 43% Full Time, and 57% Contract. Highlights an 100% In-person job distribution, with an average salary of $100,761 per year, or $48.4 per hour.

Validation Specialist / Calibration Technician (CQV, GMP, Life Sciences)

San Antonio, TX • On-site

$65K - $85K/yr

Full-time

Re-posted 3 days ago


Job description

Validation Specialist / Calibration Technician (CQV, GMP, Life Sciences)
  • Location: Texas
  • Salary: $65-85K + Bonus + Benefits

Are you looking to build a career in validation, commissioning, and qualification (CQV) within the pharmaceutical / life sciences industry? We're hiring a Validation Specialist / Calibration Technician who wants hands-on experience across IQ, OQ, PQ, exposure to real projects, and a clear path into leadership. This is an opportunity to grow quickly in a GMP-regulated environment, working alongside experienced engineers while taking ownership of meaningful validation work.
What You'll Do
  • Execute and support IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols
  • Work on validation of lab systems, equipment, and utilities
  • Partner with engineering, validation teams, and lab stakeholders
  • Assist with project scheduling, coordination, and resource planning
  • Support commissioning & qualification (CQV) activities across projects
  • Contribute to GMP / GxP documentation and compliance efforts
  • Learn to lead validation workstreams and progress into a Validation Engineer / Project Lead role
What We're Looking For
  • 2+ years of experience in:
    • Validation Engineering
    • CQV (Commissioning, Qualification, Validation)
    • or GMP-regulated environments (Pharma / Biotech)
  • Strong understanding of:
    • GMP / GxP / FDA regulations
    • Validation lifecycle (IQ/OQ/PQ)
  • Ability to work cross-functionally with engineering, QA, and operations teams
  • Strong communication and problem-solving skills
  • Coachable, driven, and motivated to grow into leadership
Requirements
  • Bachelor's degree in Engineering, Life Sciences, or related field
  • Willingness to travel regionally (project-based work)
  • Experience with validation documentation, protocols, and execution
Nice to Have
  • Experience with lab systems, utilities, or manufacturing equipment validation
  • Exposure to commissioning activities (C&Q / CQV)
  • Familiarity with AI tools for validation or documentation
Why This Role
  • Hands-on experience across pharma validation projects
  • Clear path into senior validation or project leadership roles
  • Work alongside experienced engineers in regulated environments
  • Real ownership early in your career

Validation Engineer, Validation Specialist, CQV Engineer, Commissioning Engineer, Qualification Engineer, GMP Validation, GxP, IQ OQ PQ, Pharmaceutical Validation, Life Sciences Validation, Equipment Validation, Utilities Validation, Computer System Validation, CSV Engineer, FDA Compliance, GMP Engineer
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