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Sr Validation Engineer Jobs (NOW HIRING)

GenScript/ProBio

(Sr.) Validation Engineer

Pennington, NJ · On-site

$80K - $120K/yr

The position reports to the Sr. Validation Manager and is responsible for supporting commissioning ... Coordinate validation activities with Manufacturing, Engineering, QA, QC, Automation, and external ...

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 ...

Nestle

Senior Validation Engineer

Lower Gwynedd, PA · On-site

Reporting to the Senior Manager, Facilities, Engineering and Validation, the Senior Validation Engineer role includes aspects of traditional Validation, Facilities, and Operations Engineering ...

GenScript/ProBio

(Sr.) Validation Engineer

Pennington, NJ · On-site

$80K - $120K/yr

The position reports to the Sr. Validation Manager and is responsible for supporting commissioning ... Coordinate validation activities with Manufacturing, Engineering, QA, QC, Automation, and external ...

GenScript/ProBio

(Sr.) Validation Engineer

Pennington, NJ

$80K - $120K/yr

The position reports to the Sr. Validation Manager and is responsible for supporting commissioning ... Coordinate validation activities with Manufacturing, Engineering, QA, QC, Automation, and external ...

GenScript/ProBio

(Sr.) Validation Engineer

Hopewell, NJ

$80K - $120K/yr

The position reports to the Sr. Validation Manager and is responsible for supporting commissioning ... Coordinate validation activities with Manufacturing, Engineering, QA, QC, Automation, and external ...

kindeva

Sr. Validation Engineer

Lexington, KY

As a Validation Engineer, you will play a critical role in ensuring our pharmaceutical manufacturing systems and processes meet rigorous regulatory and quality standards. You will lead and execute ...

kindeva

Sr. Validation Engineer

Lexington, KY

As a Validation Engineer, you will play a critical role in ensuring our pharmaceutical manufacturing systems and processes meet rigorous regulatory and quality standards. You will lead and execute ...

kindeva

Sr. Validation Engineer

Lexington, KY

As a Validation Engineer, you will play a critical role in ensuring our pharmaceutical manufacturing systems and processes meet rigorous regulatory and quality standards. You will lead and execute ...

Millstone

Senior Validation Engineer

Fall River, MA · On-site

Train operations personnel on validated processes, work instructions, and equipment operation to ensure compliance with established procedures. * Mentor junior engineers or technicians as needed.

kindeva

Sr. Validation Engineer

Lexington, KY

As a Validation Engineer, you will play a critical role in ensuring our pharmaceutical manufacturing systems and processes meet rigorous regulatory and quality standards. You will lead and execute ...

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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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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.

(Sr.) Validation Engineer

GenScript/ProBio

Pennington, NJ • On-site

$80K - $120K/yr

Other

Posted 18 days ago

Job description

About ProBio:

ProBio, a subsidiary of GenScript, is a global CDMO offering end-to-end services from discovery to GMP for plasmids, antibodies, and cell & gene therapies. We bring together multidisciplinary expertise to accelerate development and manufacturing through customized, and comprehensive services. ProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 150 IND approvals since October 2017

About the Job:

The position reports to the Sr. Validation Manager and is responsible for supporting commissioning, qualification, and validation (CQV) activities for GMP manufacturing facilities, utilities, equipment, computerized systems, and manufacturing processes. This position plays a key role in supporting multiple client programs across clinical and commercial manufacturing within a fast-paced CDMO environment.

Responsibilities:

  • Execute commissioning, qualification, and validation (CQV) activities for facilities, utilities, process equipment, and manufacturing systems.
  • Develop, review, and execute IQ, OQ, PQ protocols and validation reports.
  • Support facility, utility, equipment, process, cleaning, and computer system validation (CSV) activities.
  • Support technology transfer and startup activities for new client manufacturing programs.
  • Prepare validation documentation in accordance with cGMP, FDA, EU GMP, GAMP 5, and 21 CFR Part 11 requirements.
  • Support deviation investigations, CAPAs, change controls, and risk assessments related to validation activities.
  • Coordinate validation activities with Manufacturing, Engineering, QA, QC, Automation, and external vendors.
  • Participate in FAT, SAT, commissioning, equipment qualification, and facility expansion projects.
  • Maintain validation documentation and ensure data integrity throughout the validation lifecycle.
  • Support client audits, regulatory inspections, and internal quality audits.
  • Identify opportunities for continuous improvement of validation processes and engineering systems.
  • Support multiple client projects simultaneously while ensuring project timelines and quality requirements are achieved.

Qualifications:

  • BS/MS in life science or related field with 9 years of experience in drug/biologics industry in GMP production environment in roles of validation/engineering
  • Working experience in CQV for biotechnology/pharmaceutical facility is required
  • Familiar with CSV in accordance to GAMP 5 and CFR Part 11
  • Familiarity with process, cleaning, assay validation a plus
  • Experience in aseptic fill/finish equipment qualification and aseptic process simulation (APS) is preferred
  • Experience in authoring of validation protocols for utility and equipment required
  • Familiar with GMP operational principles and practice
  • Ability to work across functional groups for team collaboration

Pay range is estimated between $80k - $120k based on skill set and experience.

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