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Senior Validation Engineer Jobs in Texas (NOW HIRING)

Alcon

Senior Validation Engineer

Fort Worth, TX · On-site

The Sr. Associate, Validation (Science/Tech/Engineering Path) is primarily responsible for supporting and completing validation and qualification activities for processes, equipment, systems, and ...

New

Alcon MX

Senior Validation Engineer

Fort Worth, TX · On-site

$85 - $130/hr

The Sr. Associate, Validation (Science/Tech/Engineering Path) is primarily responsible for supporting and completing validation and qualification activities for processes, equipment, systems, and ...

New

ICU Medical

Senior Validation Engineer

Austin, TX · On-site

$110 - $150/hr

Position Summary Completes advanced validation projects with peer input and guidance from engineering and validation management.A specialist on complex technical and business matters. Work is highly ...

New

Nvidia

Senior Silicon Validation Engineer

Austin, TX · On-site

NVIDIA is seeking passionate Senior Silicon Validation Engineers to validate the world's leading GPUs and SOCs. This position offers the opportunity to have real impact in a dynamic, technology ...

Socket.dev

Sr. System/Test Validation Engineer

Austin, TX · On-site

$110 - $140/hr

Working at our manufacturing site, you will collaborate with cross-functional engineering teams and manufacturing partners to deliver scalable test strategies, automation, validation infrastructure ...

New

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Senior Validation Engineer information

See Texas salary details

$32

$60

$92

How much do senior validation engineer jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for senior validation engineer in Texas is $60.35, according to ZipRecruiter salary data. Most workers in this role earn between $48.17 and $68.51 per hour, depending on experience, location, and employer.

What does a senior validation engineer do?

A Senior Validation Engineer is responsible for ensuring that products, systems, or processes meet regulatory standards and function as intended. They develop and execute validation protocols, analyze test data, and document results to confirm compliance with industry and company standards. Senior Validation Engineers often lead validation projects, collaborate with cross-functional teams, and mentor junior staff. Their work is critical in industries like pharmaceuticals, biotechnology, and manufacturing, where product safety and efficacy are essential.

What are the key skills and qualifications needed to thrive as a senior validation engineer, and why are they important?

To thrive as a Senior Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically supported by a relevant degree and experience in validation within regulated industries. Familiarity with validation protocols (IQ, OQ, PQ), statistical analysis tools, and systems like FDA 21 CFR Part 11 is crucial. Strong problem-solving, attention to detail, and effective communication skills help ensure successful project outcomes and cross-functional collaboration. These skills and qualifications are essential to maintain product quality, meet regulatory standards, and drive continuous improvement.

What are some typical challenges faced by senior validation engineers when leading validation projects?

Senior Validation Engineers often encounter challenges such as managing tight project timelines, ensuring compliance with evolving regulatory standards, and coordinating cross-functional teams. Balancing the needs of production, quality assurance, and regulatory affairs requires strong communication and project management skills. Additionally, troubleshooting unexpected validation failures and documenting results thoroughly are key aspects that demand both technical expertise and attention to detail.

What is the difference between Senior Validation Engineer vs Validation Specialist?

AspectSenior Validation EngineerValidation Specialist
CredentialsBachelor's or Master's in Engineering, Life Sciences, or related fields; often with certifications like GxP or CSVSimilar educational background; certifications like GxP or CSV are common
Work EnvironmentDesigns and oversees validation protocols in manufacturing, biotech, or pharmaceutical settingsExecutes validation tasks, tests, and documentation in similar environments
Employer & IndustryPharmaceutical, biotech, medical device companiesSame industries, often working under validation teams
Search & ComparisonOften compared for experience level and responsibilitiesCommonly searched together for validation roles

The main difference is that a Senior Validation Engineer typically leads validation projects, designs protocols, and oversees validation activities, while a Validation Specialist focuses on executing validation tests and documentation. Both roles require similar credentials and work in comparable environments, but the Senior Validation Engineer has more responsibility for planning and oversight.

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

The most popular types of Validation Engineer jobs in Texas are:

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

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

What job categories do people searching Senior Validation Engineer jobs in Texas look for?

The top searched job categories for Senior Validation Engineer jobs in Texas are:

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

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

What are popular job titles related to Senior Validation Engineer jobs in TX?

For Senior Validation Engineer jobs in TX, the most frequently searched job titles are:

Senior Validation Engineer jobs near you
Infographic showing various Senior Validation Engineer job openings in Texas as of August 2026, with employment types broken down into 94% Full Time, 3% Part Time, and 3% Contract. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $125,518 per year, or $60.3 per hour.

Senior Validation Engineer

Alcon

Fort Worth, TX • On-site

Full-time

Medical, Life, Retirement, PTO

Posted 3 days ago

New

Alcon rating

7.5

Company rating: 7.5 out of 10

Based on 70 frontline employees who took The Breakroom Quiz

226th of 545 rated manufacturers

Job description

At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us?
This role is part of Alcon's Engineering function, a team focused on improving quality, processes, products, packaging and materials across our business to help deliver brilliant outcomes.
The Sr. Associate, Validation (Science/Tech/Engineering Path) is primarily responsible for supporting and completing validation and qualification activities for processes, equipment, systems, and facilities. You will prepare, review, and rectify validation protocols, provide technical support, and help manage department expenses.
Specifics Include:
  • Handle technical tasks, supporting operations and contributing to efficiency within defined procedures.
  • Plan, execute, and document validation studies to ensure equipment, systems, and processes operate effectively and comply with regulations.
  • Conduct risk assessments, design protocols, analyze data, and prepare validation and qualification reports.
  • Support validation activities in aseptic process management.
  • Review and approve change control documentation.
  • Provide audit support and collaborate with cross-functional teams to drive problem-solving and innovation through scientific principles.
  • Make decisions within the scope of assigned tasks, requiring advanced technical knowledge and analytical skills.
  • Perform assigned validation activities on time.
  • Handle deviations associated with these activities, if required.
  • Author complex validation protocols and technical reports (e.g. launches, transfers, weak point remediation).
  • Perform process qualification for new equipment and new technologies.
  • Participate in transfers and launches by providing data obtained during related validation activities which are needed for the registration documentation.
  • Perform or oversee risk assessments for Validation.
  • Participate in improvement and remediation of products.
  • Update documents on an as needed basis.
  • Provide Validation oversight review and approval of change control documentation.
  • Adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation.
  • Ensure rigorous quality control, complete all required training, and meet individual job requirements to contribute to overall organizational compliance.
  • Commit to continuous improvement and compliance with regulatory requirements.

WHAT YOU'LL BRING TO ALCON:
  • Bachelor's Degree or Equivalent years of directly related experience (or high school +10 yrs; Assoc.+6 yrs; M.S.+0 yrs)
  • The ability to fluently read, write, understand and communicate in English
  • 2 Years of Relevant Experience
  • Work hours: Exempt
  • Travel Requirements: None
  • Relocation assistance: No
  • Sponsorship available: No

PREFERRED QUALIFICATIONS/SKILLS/EXPERIENCE:
  • Experience working in a regulated pharmaceutical, biologics, medical device, or aseptic manufacturing environment.
  • Experience with change control, deviation investigations, CAPA, and quality management systems.
  • Proficiency in data analysis, statistical methods, and trending of validation data.
  • Experience using statistical analysis software such as Minitab.
  • Experience with temperature mapping, thermocouple data loggers, and thermal validation studies.
  • Experience with sterilization validation, including E-Beam, EO, steam, or other sterilization technologies.
  • Demonstrated project management, organizational, and cross-functional collaboration skills.
  • Ability to independently manage multiple validation projects and meet established timelines.

HOW YOU CAN THRIVE AT ALCON:
  • Join Alcon's mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career!
  • Collaborate with teammates to share standard processes and findings as work evolves!
  • See your career like never before with focused growth and development opportunities!
  • Alcon provides a robust benefits package including health, life, retirement, flexible time off for exempt associates, PTO for hourly associates, and much more!

This position may be offered at the Associate I or Associate II Engineering level, depending on the candidate's qualifications and experience.
Alcon Careers
See your impact at alcon.com/careers
ATTENTION: Current Alcon Employee/Contingent Worker
If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.
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ALCON IS AN EQUAL OPPORTUNITY EMPLOYER AND PARTICIPATES IN E-VERIFY
Alcon takes pride in maintaining an inclusive environment that values different perspectives and our policies are non-discriminatory in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.

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