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Senior Validation Engineer Jobs (NOW HIRING)

NVIDIA

Senior Validation Engineer

Hillsboro, OR · On-site

Become part of NVIDIA's world-class team as a Senior Validation Engineer in Hillsboro! For 25 years, our company has changed computer graphics, PC gaming, and accelerated computing. Driven by an ...

TekWissen LLC

Senior Validation Engineer

Portsmouth, NH · On-site

$35 - $45/hr

Senior Validation Engineer Location: Portsmouth, NH - 03801 Duration: 7 Months Job Type: Temporary Assignment Work Type: Hybrid Summary The CSV Engineer will act as an individual contributor ...

Nvidia

Senior Validation Engineer

Hillsboro, OR · On-site

Become part of NVIDIA's world-class team as a Senior Validation Engineer in Hillsboro! For 25 years, our company has changed computer graphics, PC gaming, and accelerated computing. Driven by an ...

LG Electronics

Sr. Validation Engineer

Aliso Viejo, CA · On-site

$87K - $116K/yr

A leading provider of core components for global car manufacturers, VS Company is supporting the emerging trend of the vehicle industry. Sr. Validation Engineer * Perform validation for infotainment ...

Alcami Corporation

The Sr. Validation Engineer will execute protocols for Installation, Operational and Performance Qualification testing on chambers and rooms including: cryo-freezers, cold rooms, refrigerators ...

Kasmo Global

Validation engineer

College Station, TX · On-site

Senior Validation Engineer The Senior Validation Engineer, with minimal supervision, is a non-supervisory role and will be responsible for drafting Validation Project Plans (VPPs), System Impact ...

Proterra, Inc.

Sr. Validation Engineer

Greer, SC

As a Senior Validation Engineer, you will own testing and validation across the full battery lifecycle -- from modules to complete pack-level systems. You will work shoulder-to-shoulder with ...

Proterra

Sr. Validation Engineer

Greer, SC · On-site

As a Senior Validation Engineer, you will own testing and validation across the full battery lifecycle - from modules to complete pack-level systems. You will work shoulder-to-shoulder with ...

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How much do senior validation engineer jobs pay per hour?

As of Jun 5, 2026, the average hourly pay for senior 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 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 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 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.

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Senior Validation Engineer jobs near you
Infographic showing various Senior Validation Engineer job openings in the United States as of May 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $134,726 per year, or $64.8 per hour.
Sr. Validation Engineer

Sr. Validation Engineer

Pyramid Laboratories Inc

Costa Mesa, CA • On-site

$110K - $125K/yr

Full-time

Posted 15 days ago

Job description

Position Summary

The Senior Validation Engineer is responsible for leading and executing validation activities supporting sterile injectable and biopharmaceutical manufacturing operations. This role ensures that facilities, utilities, equipment, computerized systems, and processes are designed, installed, qualified, and maintained in a validated state in compliance with FDA, EU GMP, ICH, and other global regulatory requirements. The position provides technical leadership, cross-functional collaboration, and subject matter expertise for aseptic processing, cleanroom environments, and contamination control strategies.

Key Responsibilities

Validation & Qualification

  • Lead and execute DQ, IQ, OQ, and PQ activities for aseptic filling lines and isolators/RABS, Autoclaves, SIP/CIP systems, Lyophilizers, Sterile filtration systems, cleanrooms and classified areas.
  • Author, review, and approve validation protocols, perform and support executions, interpret and review data, and write final reports.
  • Develop and maintain Validation Master Plans (VMPs).
  • Experience with process and cleaning validations and aseptic process simulations (media fills).
  • Lead validation of critical utilities such as Water for Injection (WFI), clean steam, HVAC systems and Compressed gases (CDA, and nitrogen).
    • Execute environmental qualification and airflow visualization (smoke studies).
    • Validate computerized systems in accordance with GAMP 5 and 21 CFR Part 11.
    • Ensure data integrity compliance (ALCOA+ principles).
    • Support automation and control systems validation (PLC, SCADA, etc.).
    • Ensure validation activities comply with FDA cGMPs (21 CFR Parts 210, 211), and EU GMP Annex 1 (Sterile Manufacturing).
    • Support regulatory inspections, customer audits and responses to audits.

Technical Leadership & Continuous Improvement

  • Act as Subject Matter Expert (SME) for validation and sterile manufacturing.
  • Lead change controls, deviations, CAPAs, and risk assessments (FMEA).
  • Drive continuous improvement initiatives to enhance compliance, efficiency, and robustness.

Required Education

  • Bachelor’s degree in Engineering or related Life Sciences field.
  • Excellent technical writing and documentation skills and MS Office (Word, Excel, PowerPoint, etc.).

Experience

  • 7+ years of hands-on experience in validation of sterile injectable pharmaceutical or biopharmaceutical industry.