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Sr Validation Engineer Jobs in Edison, NJ (NOW HIRING)

CAI

Senior Validation Engineer

Bridgewater, 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

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

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

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 ...

Catapult

Senior Validation Manager

Princeton, NJ · On-site

The Senior Validation Manager is leading the site validation program and all qualification and ... Lead all validation activities in a hands-on approach and in collaboration with the engineering and ...

Catapult

Senior Validation Manager

Princeton, NJ · On-site

The Senior Validation Manager is leading the site validation program and all qualification and ... Lead all validation activities in a hands-on approach and in collaboration with the engineering and ...

WuXi Biologics

Senior Engineer l, Validation

Cranbury, NJ · On-site

$73K - $117K/yr

Job Title - Senior Engineer l, Validation Work Location - Cranbury NJ Job Summary The Validation Engineer supports the successful operation of facility, laboratory, cGMP Manufacturing and business ...

DTCC

Model Validation Senior Associate

Jersey City, NJ · On-site

Per the Federal Reserve Supervision and Regulator guidance (SR 11-7), Model Validation is the set ... Work with the model owner, model developer, and model user on all aspects of model validation and ...

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All JobsSr Validation Engineer JobsSr Validation Engineer Jobs in Edison, NJ

Sr Validation Engineer information

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How much do sr validation engineer jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for sr validation engineer in Edison, NJ is $65.69, according to ZipRecruiter salary data. Most workers in this role earn between $52.40 and $74.62 per hour, depending on experience, location, and employer.

What is a Sr validation engineer?

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?

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 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 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.

What are popular job titles related to Sr Validation Engineer jobs in Edison, NJ?

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What job categories do people searching Sr Validation Engineer jobs in Edison, NJ look for?

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What cities near Edison, NJ are hiring for Sr Validation Engineer jobs?

Cities near Edison, NJ with the most Sr Validation Engineer job openings:

Sr Validation Engineer jobs near you
Infographic showing various Sr Validation Engineer job openings in Edison, NJ as of August 2026, with employment types broken down into 86% Full Time, 7% Part Time, 3% Temporary, and 4% Contract. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $136,630 per year, or $65.7 per hour.

Sr. Validation Engineer

Sunrise Systems Inc.

Branchburg, NJ • On-site

Full-time

Re-posted 29 days ago

Job description

Company Description
Sunrise Systems was founded in 1990 with a vision to deliver world class staffing services and solutions in all categories, including leading edge IT consulting and solutions, with the commitment to deliver service that exceeds expectations and become the most trusted name in the industry. Today, two and a half decades later, we pride ourselves on being the forerunner in the staffing and Information Technology business. We combine our deep industry expertise, insight and global resources to build the best workforce for our clients and by connecting them with the perfect professionals across different industry verticals.
Job Description
Summary:
  • Responsible for but not limited to, working under operations engineering department in developing and executing process and equipment validation protocols, as applicable to ensure compliance to applicable regulatory requirements, internal company standards and industry practices.
  • As a member of Operation team, responsible for developing /supporting of revenue and process improvement projects and executing IQ/OQ/PQ protocols including temperature mapping for storage equipment and facilities, as applicable, and making recommendations for changes and/or improvements.
  • Ensure project completion per schedule, overall compliance and continuous quality and product/process improvement in an ever-changing, regulated environment.
  • Essential Job Functions: This is not intended as a comprehensive list; it is intended to provide a representative summary of the major duties and responsibilities and incumbent(s) may be required to perform additional, position-specific tasks.
  • Develop and execute validation protocols (IQ/OQ/PQ/PPQ/PV) and test scripts for all applicable equipment, systems, products and processes, temperature mapping, including required annual re-qualifications and writing final validation reports.
  • Work with the Sr. Validation Engineer / Manager for Validation services and other Operation Engineering and Quality Management in the development of Validation Plans, Documents & Reports/Records.
  • Develop and perform engineering studies for improvements of equipment performance or process capabilities to reduce costs and cycles with ensuring validations.
  • Assess effectiveness via auditing and validations of systems with respect to all relevant guidance, regulations, standards and requirements.
  • Work with Manager of Validation services to ensure consistency of systems/practices across product lines and their conformance to regulations and other industry practices and identify area of continuous improvement.
  • Technical writing of Quality, Equipment and Processing Operating Procedures (SOP), Component Specifications and other documentation, as required.
  • Maintain a thorough knowledge and understanding of the following regulations and guidelines: FDA 21 CFR 1270 and 1271 - Current Good Tissue Practices, American Association of Tissue banks for Tissue banking, 21 CFR 820 - Medical Devices - Quality System Regulations, ISO 9001 - Quality Management Standards, ISO 9001 Quality Management System Standards, ISO 13485 - Medical Device - Quality Management System, ISO Clean Room Standards and others as required.
  • Partner and practice in the Operation Engineering, Manufacturing and Quality along with Quality Planning process for LifeCell's Quality Management System and support the entire manufacturing/operations and quality effort at LifeCell.
  • Develop and / or Revise manufacturing and engineering documentation, ensuring compliance between manufacturing process documentation, all applicable specifications, and engineering drawings while providing required operator training.
  • Experience in managing Quality Investigation (QI and Corrective and Preventative Actions (CAPA) and collaborating with quality and manufacturing in the root cause verification and corrective action implementation.
  • Lead and effectively interface with Manufacturing/Production, Maintenance, Quality, external vendors, and other support teams to complete projects meeting with production, quality, cost savings, and new product / process development goals within schedule and budget.

Qualifications
University Degree:
  • BS in Engineering or other sciences. Higher degree will be a plus.
  • Experience: 5 to 7 years of experience in validation and quality related field.

Other Required Skills:
  • Proficiency in Microsoft office tools (Excel, Word, Power Point, Access, Project), Track Wise and Oracle Use.
  • Use of statistics techniques for sampling plan will be a plus.
  • Grasps concepts quickly especially related to Federal, AATB, ISO and other regulatory guidelines including understanding of the various regulations and guidelines such as FDA 21 CFR 1270 and 820, ISO 13485 and others as required.
  • Self-starter with excellent technical writing, analytical and interpersonal skills to allow effective participation in project teams and project execution.

Additional Information
All your information will be kept confidential according to EEO guidelines.

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