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Sr Validation Engineer Jobs (NOW HIRING)

Sigan America LLC

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Validation Engineer

Ottawa, IL · On-site

$90K - $100K/yr

Senior Validation Engineer Location: Ottawa, Illinois Employment Type: Full-Time About the Position We are seeking an experienced Senior Validation Engineer to lead validation activities supporting ...

CAI

Senior Validation Engineer

Princeton, NJ

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Cincinnati, OH

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Cincinnati, OH

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Bridgewater, NJ

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Princeton, NJ · On-site

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Raleigh, NC

$87K - $120K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Kenosha, WI · On-site

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Philadelphia, PA

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Charlotte, NC

$87K - $120K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

Alphatec Spine

Validation Engineer II

Carlsbad, CA

Seeks guidance from and collaborates with senior validation engineers; may informally assist with onboarding or knowledge sharing for newer team members. * Maintains regular and consistent attendance ...

CAI

Senior Validation Engineer

Charlotte, NC

$87K - $120K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Greenville, NC

$87K - $120K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Indianapolis, IN

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Indianapolis, IN

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Harrisburg, PA

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Bloomington, IN

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Philadelphia, PA

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Greenville, NC

$87K - $120K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

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Sr Validation Engineer information

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How much do sr validation engineer jobs pay per hour?

As of Jul 19, 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.

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What cities are hiring for Sr Validation Engineer jobs? Cities with the most Sr Validation Engineer job openings:
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Sr Validation Engineer jobs near you
Infographic showing various Sr Validation Engineer job openings in the United States as of July 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $134,726 per year, or $64.8 per hour.
Validation Engineer

Validation Engineer

Sigan America LLC

Ottawa, IL • On-site

$90K - $100K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 24 days ago

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Job description

Senior Validation Engineer

Location: Ottawa, Illinois
Employment Type: Full-Time

About the Position

We are seeking an experienced Senior Validation Engineer to lead validation activities supporting our cGMP manufacturing operations. This role is responsible for validating equipment, facilities, utilities, manufacturing processes, and computerized systems while ensuring compliance with FDA cGMP requirements and industry best practices.

The ideal candidate has a strong technical background in pharmaceutical, medical device, cosmetic, or regulated manufacturing environments and enjoys working cross-functionally with Engineering, Quality, Manufacturing, Regulatory Affairs, Maintenance, and R&D.

Key Responsibilities

  • Develop, review, and execute IQ, OQ, and PQ validation protocols.
  • Plan and execute validation activities for new equipment, facilities, utilities, and manufacturing processes.
  • Support new product launches and continuous process improvement initiatives.
  • Prepare validation reports and maintain complete validation documentation.
  • Lead equipment qualification and process validation projects from planning through implementation.
  • Support engineering change controls and assess validation impact for equipment and process changes.
  • Perform periodic reviews and revalidation of equipment, utilities, and manufacturing processes.
  • Ensure compliance with FDA cGMP regulations, ISPE guidance, and internal quality standards.
  • Maintain validation records, equipment logbooks, and supporting documentation.
  • Collaborate with Maintenance, Engineering, Manufacturing, Quality Assurance, Regulatory Affairs, and R&D to resolve technical issues and implement improvements.
  • Identify opportunities to improve validation systems, documentation, and overall compliance.

Systems & Equipment Experience

Experience validating one or more of the following is highly desirable:

  • HVAC systems
  • Purified Water / RODI Water Systems
  • Compressed Air and Gas Systems
  • Boilers and Chillers
  • Temperature- and Humidity-Controlled Rooms
  • Refrigerators, Freezers, and Incubators
  • Manufacturing Equipment
  • Laboratory Equipment
  • Computerized Systems and 21 CFR Part 11 Compliance

Qualifications

Required

  • Bachelor's degree in Engineering, Life Sciences, or a related technical field (or equivalent experience).
  • 3–5+ years of validation experience in a pharmaceutical, medical device, cosmetic, or other FDA-regulated manufacturing environment.
  • Experience developing and executing IQ/OQ/PQ protocols.
  • Experience with equipment, facility, utility, and process validation.
  • Experience with engineering change controls and validation documentation.
  • Strong technical writing and documentation skills.
  • Excellent organizational skills with exceptional attention to detail.
  • Ability to manage multiple projects while meeting deadlines.

Preferred

  • Experience performing temperature mapping of refrigerators, freezers, incubators, warehouses, or controlled environments.
  • Experience with software validation and 21 CFR Part 11 compliance.
  • Experience completing validation periodic reviews.
  • Knowledge of risk-based validation methodologies.
  • Familiarity with Lean Manufacturing or Continuous Improvement initiatives.

What We're Looking For

The successful candidate is a hands-on validation professional who enjoys solving technical problems, improving manufacturing processes, and working collaboratively across departments. This individual is organized, detail-oriented, and committed to maintaining the highest standards of quality and regulatory compliance.

Competitive salary and comprehensive benefits package offered based on experience.

Company Description

About Us
Fast growing liquid pour contract manufacturer of premium health and beauty products.