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Qa Validation Engineer Jobs in New York (NOW HIRING)

Jj

QA Validation Specialist II LVV

Raritan, NJ · On-site

... QA Validation Specialist II LVV! .This position will be located in Raritan, NJ. At the Janssen ... A minimum of a Bachelor's Degree is required, with a focused degree in Engineering, Science or ...

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Argyllinfotech

QA Engineer

New York, NY · On-site

Position: QA Engineer - Data Pipeline, Kafka & AWS Location New York City/Dallas TX/St. Louis MO ... The ideal candidate will be responsible for validating data ingestion, transformation, processing ...

Cantor Fitzgerald Securities

QA Engineer

Manhattan, NY · On-site

As a Senior QA Engineer, you will play a crucial role in validating FMX's trading platforms and ensuring their reliability in high-stakes environments. Your expertise in manual testing, trading ...

Cantor Fitzgerald Securities

QA Engineer

Manhattan, NY · On-site

As a Senior QA Engineer, you will play a crucial role in validating FMX's trading platforms and ensuring their reliability in high-stakes environments. Your expertise in manual testing, trading ...

AaraTechnologies Inc

QA ENGINEER

Jersey City, NJ · On-site

You will work closely with developers and analysts in Agile teams. Ideal for early-career QA ... Validate data and reports * Maintain test documentation * Collaborate with project teams Required ...

AaraTechnologies Inc

QA ENGINEER

Jersey City, NJ · On-site

Validate healthcare data and reporting outputs * Identify, log, track, and retest defects * Support ... Collaborate with developers, analysts, and business teams * Maintain test documentation and QA ...

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Qa Validation Engineer information

What is a QA Validation Engineer?

QA Validation Engineers are professionals responsible for ensuring that products, systems, or software meet specified quality and regulatory standards before they are released or deployed. They design and execute validation protocols, document results, and identify any issues or non-conformities during the testing process. Their role is crucial in industries like pharmaceuticals, manufacturing, and software, where compliance and reliability are essential. QA Validation Engineers collaborate closely with development, production, and regulatory teams to ensure that products are safe, effective, and meet all necessary guidelines.

How does a QA Validation Engineer typically collaborate with cross-functional teams during product development?

As a QA Validation Engineer, you’ll work closely with development, regulatory, and operations teams to ensure products meet quality and compliance standards. You’ll participate in project meetings, review technical documentation, and provide input on test strategies and validation protocols. Effective communication and problem-solving are essential, as you may need to clarify requirements, address issues found during validation, and coordinate testing activities. This collaborative environment helps ensure that products are released on schedule and comply with industry regulations.

What are the key skills and qualifications needed to thrive as a QA Validation Engineer, and why are they important?

To thrive as a QA Validation Engineer, you need a solid understanding of quality assurance methodologies, validation protocols, and a relevant technical degree such as in engineering or life sciences. Familiarity with industry regulations (such as FDA or ISO standards), validation management software, and documentation tools is typically required. Attention to detail, analytical thinking, and strong communication skills help you excel in identifying compliance gaps and collaborating with cross-functional teams. These skills and qualities are crucial to ensure products meet regulatory requirements and maintain high standards of quality and safety.

What is the difference between Qa Validation Engineer vs QA Tester?

AspectQa Validation EngineerQA Tester
CertificationsISTQB, CQE, or similarISTQB Foundation, CSTE
Work EnvironmentRegulatory, validation-focused industries like pharma, biotechSoftware development, IT, web applications
ResponsibilitiesValidating systems, ensuring compliance, writing validation protocolsExecuting test cases, identifying bugs, reporting issues

While both roles focus on quality assurance, Qa Validation Engineers primarily work on validating systems for compliance and regulatory standards, often in industries like pharmaceuticals. QA Testers concentrate on testing software functionality and identifying bugs during development. The roles overlap in testing skills but differ in scope and industry focus.

Are QA Validation Engineers in demand?

QA Validation Engineers are in demand across industries such as pharmaceuticals, biotech, and manufacturing, where regulatory compliance and quality assurance are critical. The role requires knowledge of validation processes, testing protocols, and often involves working with tools like GxP standards and validation software, making experienced professionals highly sought after.

Do validation engineers make good money?

Validation engineers, including QA validation engineers, typically earn competitive salaries that vary by industry, experience, and location. They often require knowledge of testing tools, validation protocols, and quality standards, which can influence compensation levels. Overall, validation engineering is considered a well-paying profession within quality assurance and engineering fields.

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

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

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

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

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

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

Qa Validation Engineer jobs near you
Infographic showing various Qa Validation Engineer job openings in New York as of August 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution.

Quality Assurance Validation Manager

Thermo Fisher Scientific

Teterboro, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 26 days ago

Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 429 frontline employees who took The Breakroom Quiz

170th of 545 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Location: Ridgefield, New Jersey - Sterile Fill-Finish & Packaging Site
Our state-of-the-art sterile fill-finish and packaging facility in Ridgefield, NJ, is dedicated to meeting the growing needs of biotech and pharmaceutical drug developers. With expanded capabilities in pre-filled syringe and liquid vial manufacturing, the site increases U.S. capacity to manufacture the medicines patients rely on every day.
As part of Thermo Fisher Scientific's global network, Ridgefield complements our world-class contract development and manufacturing services and strengthens our sterile fill-finish footprint-now spanning seven sites worldwide, including three in the U.S. (Greenville, NC; Plainville, MA; and Ridgefield, NJ). Strategically located along the East Coast to streamline logistics and attract top talent, the 360,000 sq. ft. Ridgefield site plays a vital role in the global pharmaceutical supply chain, with products distributed to more than 67 countries across all continents.
Join Thermo Fisher Scientific and play a critical role in supporting the delivery of life-changing therapies and products to patients worldwide. As a Quality Assurance Validation Manager, you will lead validation activities that ensure product quality, operational excellence, and compliance with global regulatory requirements. Working in a highly collaborative environment, you will partner with Quality Assurance, Manufacturing, Engineering, Regulatory Affairs, and other cross-functional teams to maintain the validated state of systems and processes that support the manufacture of therapeutics and other critical products.
You'll have the opportunity to influence validation strategy, lead complex projects, and develop a high-performing team while contributing to a culture of quality, continuous improvement, and innovation.
Discover Impactful Work:
As a Quality Assurance Validation Manager, you will provide leadership and oversight for validation programs across equipment, utilities, facilities, computer systems, cleaning processes, analytical instruments, and manufacturing operations. You will ensure validation activities are executed in accordance with cGMP requirements, quality standards, and industry best practices while supporting business objectives, new product introductions, and technology transfer initiatives. In partnership with Quality Assurance and cross-functional teams, you will help maintain compliance and the validated state of critical systems and processes that support the manufacture of therapeutics and other life-changing products.
A Day in the Life:
  • Lead and manage validation activities across manufacturing, laboratory, utility, facility, computerized systems, and analytical instruments
  • Develop and maintain validation strategies, validation master plans, and project timelines
  • Oversee the planning, coordination, execution, review, and approval of validation protocols and reports
  • Partner with project managers and cross-functional stakeholders to establish priorities, monitor progress, and communicate project status
  • Ensure validation activities comply with FDA, EU, and applicable global regulatory requirements and Quality Assurance standards
  • Support equipment qualification, process validation, cleaning validation, utility qualification, computer system validation, and analytical instrument qualification programs
  • Apply risk assessment methodologies and statistical tools to support validation decisions
  • Drive continuous improvement initiatives to enhance validation processes and operational efficiency
  • Manage change control activities and assess validation impacts associated with process or system changes
  • Ensure adherence to data integrity requirements and governance standards across validation activities
  • Support regulatory inspections, customer audits, and quality assessments
  • Mentor, develop, and lead validation professionals while fostering a culture of accountability and excellence

Keys to Success:
Education
  • Advanced Degree with 8+ years of validation experience, or
  • Bachelor's Degree with 10+ years of validation experience
  • Preferred fields of study include Engineering, Chemistry, Biology, Life Sciences, or related technical disciplines

Experience
  • Significant experience in validation within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments
  • Experience coordinating, planning, executing, and approving validation activities across multiple disciplines
  • Demonstrated success managing complex validation projects, programs, and teams
  • Experience partnering with project managers to establish priorities and drive project execution
  • Experience participating in regulatory inspections and customer audits
  • Experience with validation master planning, change control systems, and quality management systems
  • Expertise in process validation and analytical instrument qualification
  • Proficiency in data integrity compliance, governance, and regulatory expectations related to data lifecycle management

Knowledge, Skills, Abilities
  • Strong knowledge of cGMP regulations, including FDA, EU, and global regulatory requirements
  • Expertise in equipment qualification, process validation, cleaning validation, computer system validation, utility qualification, and analytical instrument qualification
  • Strong understanding of ALCOA+ principles, data integrity requirements, and data governance practices
  • Proficiency in risk assessment methodologies and statistical analysis
  • Strong technical writing, documentation, and report review capabilities
  • Excellent leadership, communication, and interpersonal skills
  • Ability to influence stakeholders and collaborate effectively across functions and organizational levels
  • Knowledge of Lean Manufacturing and continuous improvement methodologies
  • Proficiency with Microsoft Office and standard business software applications
  • Strong organizational and problem-solving skills with the ability to manage multiple priorities

Relocation assistance is not provided
Must be legally authorized to work in the United States now or in the future without sponsorship
Must be able to pass a comprehensive background check, which includes a drug screening
Compensation and Benefits
The salary range estimated for this position based in New Jersey is $112,500.00-$168,750.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs
  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement
  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
  • Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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