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Validation Engineer Jobs in Edison, NJ (NOW HIRING)

ZT Systems

Mechanical Validation Engineer

Secaucus, NJ · On-site

The Mechanical Validation Engineer will be working with cross functional teams to aid in developing as well as executing test plans which will verify product hardware functionality, adherence to ...

ZT Systems

Electrical Validation Engineer

Secaucus, NJ · On-site

The Electrical Validation Engineer will be working with cross functional teams to aid in developing as well as executing test plans which will verify product hardware functionality, adherence to ...

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 ...

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 ...

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Validation Engineer information

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How much do validation engineer jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for validation engineer in Edison, NJ is $53.83, according to ZipRecruiter salary data. Most workers in this role earn between $40.82 and $65.43 per hour, depending on experience, location, and employer.

What is a validation engineer?

A validation engineer is responsible for testing equipment and electrical systems used in the manufacturing process. As a validation engineer, your primary duty is to work with the other members of the validation team to ensure that these systems measure up to company and industry standards. Skills needed for a validation engineer job include the ability to accurately test, measure, and calibrate manufacturing equipment for maximum efficiency and quality.

What are the key skills and qualifications needed to thrive as a validation engineer, and why are they important?

To thrive as a Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically backed by a degree in engineering or a related field. Familiarity with validation protocols, statistical analysis tools, and industry-specific regulations such as FDA, GMP, or ISO standards is essential. Strong analytical thinking, attention to detail, and effective communication set top performers apart in this role. These skills ensure that products and processes meet stringent quality and safety standards, minimizing risks and ensuring regulatory approval.

What are some common challenges validation engineers face when working cross-functionally with other departments?

Validation Engineers frequently collaborate with teams such as manufacturing, quality assurance, and research & development. One common challenge is aligning differing priorities and timelines between departments, which can sometimes delay validation projects. Effective communication skills and flexibility are crucial to navigating these cross-functional interactions, ensuring that all regulatory and quality requirements are met without hindering production schedules. Building strong working relationships and proactively addressing potential concerns can help Validation Engineers facilitate smoother project execution.

What is the difference between Validation Engineer vs Quality Assurance Engineer?

AspectValidation EngineerQuality Assurance Engineer
CertificationsGMP, ISO, Six SigmaISO, Six Sigma, CQA
Work EnvironmentRegulated industries like pharma, biotech, medical devicesManufacturing, software, and product development
Primary FocusEnsuring products meet specifications through validation processesPreventing defects through process and system improvements
Common UsageRegulatory compliance, validation protocolsProcess audits, quality systems

Validation Engineers focus on verifying that products and processes meet regulatory standards through validation protocols, especially in regulated industries. Quality Assurance Engineers concentrate on maintaining overall product quality by implementing and auditing quality systems. While both roles aim to ensure product safety and efficacy, Validation Engineers are more involved in validation activities, whereas QA Engineers focus on process improvement and defect prevention.

Is validation engineer a good job?

Validation engineers are responsible for ensuring that products and processes meet quality standards through testing and documentation, often in regulated industries like pharmaceuticals or manufacturing. The role typically requires attention to detail, knowledge of validation protocols, and familiarity with tools like GxP or FDA regulations. It can offer stable employment and opportunities for specialization and advancement.

What degree do you need to be a validation engineer?

Validation engineers typically hold a bachelor's degree in engineering, life sciences, or a related field. Some roles may require a master's degree or specialized certifications in quality assurance or validation processes. Strong knowledge of industry standards and experience with validation tools are also important.
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Validation Engineer jobs near you
Infographic showing various Validation Engineer job openings in Edison, NJ as of August 2026, with employment types broken down into 91% Full Time, 5% Part Time, and 4% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $111,965 per year, or $53.8 per hour.

Sr. Validation Engineer

Sunrise Systems Inc.

Branchburg, NJ • On-site

Full-time

Re-posted 19 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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