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Sr Validation Engineer Jobs (NOW HIRING)

This is Mahaboob from Intellectt INC; we've got an important Senior Validation Engineer - Oregon with one of our prestigious clients. Interested candidates can please send your updated resume at ...

Valira LLC, has openings in Chalfont, PA. Sr. Validation Engineer ($124,238.00/Yr.): Validate, Review, Quality, Involve, Responsible, Authority, Manage, Work, Change and Perform validation test ...

Valira LLC, has openings in Chalfont, PA. Sr. Validation Engineer ($124,238.00/Yr.): Validate, Review, Quality, Involve, Responsible, Authority, Manage, Work, Change and Perform validation test ...

The Senior Validation Engineer will be part of a cross functional team that will plan and execute commissioning/qualification (CQ) projects for equipment and critical utilities process, tech transfer ...

Validation Engineer

Kenosha, WI · On-site

$50 - $55/hr

Mostly overnight shifts, 12-hour shifts Openings: 5 Experience: 3+ years for Validation Engineer or 5+ years for Senior Validation Engineer About the Role We are hiring experienced Validation ...

The Senior Validation Engineer will be part of a cross functional team that will plan and execute commissioning/qualification (CQ) projects for equipment and critical utilities process, tech transfer ...

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Sr Validation Engineer information

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How much do sr validation engineer jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for sr validation engineer in the United States is $64.77, according to ZipRecruiter salary data. Most workers in this role earn between $51.68 and $73.56 per hour, depending on experience, location, and employer.

What are some common challenges a Sr Validation Engineer faces when managing multiple validation projects simultaneously?

A Sr Validation Engineer often manages several validation projects at once, which can present challenges such as coordinating timelines, ensuring compliance with regulatory standards, and balancing cross-functional communication. Keeping detailed documentation and staying organized are essential, as unexpected equipment issues or shifting project priorities may arise. Successful engineers proactively communicate with quality, manufacturing, and R&D teams to mitigate risks, maintain project momentum, and deliver results within required deadlines.

What are Sr Validation Engineers?

Sr Validation Engineers are experienced professionals responsible for ensuring that products, systems, or processes meet regulatory standards and function as intended. They lead validation projects, develop protocols, oversee testing, and document results to confirm compliance with industry regulations, such as those from the FDA or ISO. Their work is essential in industries like pharmaceuticals, biotechnology, and manufacturing, where product quality and safety are critical. Senior validation engineers also mentor junior staff and help improve validation processes within their organizations.

What are the key skills and qualifications needed to thrive as a Sr Validation Engineer, and why are they important?

To thrive as a Sr Validation Engineer, you need a solid background in engineering or life sciences, extensive experience with validation protocols, and a strong understanding of regulatory standards such as FDA, GMP, or ISO. Expertise in using validation software, risk assessment tools, and familiarity with documentation management systems is typically required, along with certifications like Six Sigma or ASQ CQE being advantageous. Exceptional problem-solving abilities, attention to detail, and effective communication skills help you lead teams and interact with cross-functional departments. These competencies are crucial for ensuring products and processes meet compliance standards, maintain quality, and support organizational success.

What is the difference between Sr Validation Engineer vs Validation Engineer?

AspectSr Validation EngineerValidation Engineer
Required CredentialsBachelor's/Master's in Engineering, certifications like CQE or ASQ, experience in validation processesBachelor's in Engineering or related field, some certifications preferred, less experience required
Work EnvironmentPharmaceutical, biotech, or manufacturing industries; leading validation projectsSupporting validation tasks under supervision, often in similar industries
Employer & Industry UsageUsed by companies requiring compliance with FDA, ISO, or GMP standardsCommonly used in manufacturing and quality assurance roles

The main difference between a Sr Validation Engineer and a Validation Engineer lies in experience, responsibility, and expertise. The Sr Validation Engineer typically leads validation projects, has more advanced certifications, and plays a strategic role in compliance. Validation Engineers support validation activities and often work under supervision. Both roles are essential in regulated industries like pharmaceuticals and manufacturing, but the senior role involves greater leadership and technical oversight.

More about Sr Validation Engineer jobs
What cities are hiring for Sr Validation Engineer jobs? Cities with the most Sr Validation Engineer job openings:
What states have the most Sr Validation Engineer jobs? States with the most job openings for Sr Validation Engineer jobs include:
Infographic showing various Sr Validation Engineer job openings in the United States as of May 2026, with employment types broken down into 98% Full Time, 1% Part Time, and 1% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $134,726 per year, or $64.8 per hour.
Senior Validation Engineer

Senior Validation Engineer

Intellectt INC

Portland, OR • On-site

Contractor

Posted 8 days ago


Job description

Hello, 
I Hope you are doing great. 

This is Mahaboob from Intellectt INC; we’ve got an important Senior Validation Engineer - Oregon with one of our prestigious clients. Interested candidates can please send your updated resume at mahaboob.m@intellectt.com

Title: Senior Validation Engineer
Location: Oregon

Summary: Seeking a Senior Validation Engineer with strong GMP experience to support QC equipment validation and Computer System Validation (CSV) activities.
Key Responsibilities:

  • Author & execute URS, IQ/OQ/PQ, risk & data integrity assessments
  • Support CSV (ValGenesis preferred)
  • Manage full lifecycle of QC equipment (qualification to requalification)
  • Support analytical method transfers & vendor coordination
  • Ensure compliance with GMP & ALCOA+

Requirements:

  • 5+ years validation experience in GMP environment
  • Hands-on with HPLC, GC, bioassay systems
  • Strong CQV, QC Equipment & CSV experience

Thanks & Regards,
Mahaboob M
Technical Recruiter
Intellectt Inc 
mahaboob.m@intellectt.com
Direct: 732-276-1830
Desk number: 732 412 6999- Ext: 355