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Senior Validation Engineer Jobs in New York (NOW HIRING)

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

Bridgewater, NJ

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

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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Senior Validation Engineer information

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How much do senior validation engineer jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for senior validation engineer in New York is $70.86, according to ZipRecruiter salary data. Most workers in this role earn between $56.54 and $80.48 per hour, depending on experience, location, and employer.

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 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 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.

What are the most commonly searched types of Validation Engineer jobs in New York?

The most popular types of Validation Engineer jobs in New York are:

What are popular job titles related to Senior Validation Engineer jobs in New York?

For Senior Validation Engineer jobs in New York, the most frequently searched job titles are:

What job categories do people searching Senior Validation Engineer jobs in New York look for?

The top searched job categories for Senior Validation Engineer jobs in New York are:

What cities in New York are hiring for Senior Validation Engineer jobs?

Cities in New York with the most Senior Validation Engineer job openings:

What are popular job titles related to Senior Validation Engineer jobs in NY?

For Senior Validation Engineer jobs in NY, the most frequently searched job titles are:

Senior Validation Engineer jobs near you
Infographic showing various Senior Validation Engineer job openings in New York as of August 2026, with employment types broken down into 90% Full Time, 6% Part Time, and 4% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $147,395 per year, or $70.9 per hour.

Sr. Validation Engineer

Sunrise Systems Inc.

Branchburg, NJ • On-site

Full-time

Re-posted 12 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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