Validation Engineer Jobs in New York
Validation Engineer jobs in New York are in strong demand, concentrated in pharmaceutical and biotechnology manufacturing, medical device production, and regulated food and beverage industries, with openings at every level from entry-level associate to senior process validation engineer. The heaviest hiring activity is in the New York City metro, Long Island's biopharma corridor around Hauppauge and Melville, and the Hudson Valley, where manufacturers like Pfizer, Bristol Myers Squibb, and Regeneron maintain large validation teams. The most sought-after specialties in New York listings are computer system validation, process validation for aseptic manufacturing, and equipment qualification under FDA 21 CFR Part 11 compliance. Find a role that fits below and apply directly.
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Showing 5 of 9+ Validation Engineer jobs
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)Job Description
Validation Engineer II
Grand Island, NY | On-site - Relocation assistance is not available.
Candidates must be legally authorized to work in the United States without sponsorship.
Employment is contingent upon successful completion of applicable pre-employment requirements, including a background check and drug screening.
Build Your Career in Validation. Make an Impact That Matters.
At Thermo Fisher Scientific, your engineering work helps enable our customers to make the world healthier, cleaner and safer.
We are looking for a Validation Engineer II to join our Grand Island manufacturing team. This is an excellent opportunity for an early-career engineer or validation professional who wants to build valuable experience in GMP manufacturing, equipment and facility qualification, process validation, capital projects and continuous improvement.
You’ll work directly with Engineering, Manufacturing, Quality, Maintenance and Automation teams and gain hands-on exposure to projects that have a meaningful impact on our operations and the customers we serve.
What You’ll Do
As a Validation Engineer II, you will help ensure our manufacturing equipment, facilities, utilities and processes operate reliably and meet applicable quality and regulatory requirements.
You will:
Develop and execute validation and qualification activities for manufacturing equipment, facilities, utilities and processes.
Author and execute IQ, OQ and PQ protocols, validation plans and summary reports.
Support the commissioning, startup and qualification of new equipment and facility improvements.
Partner with Engineering, Manufacturing, Quality, Maintenance and Automation teams to solve technical problems and successfully deliver projects.
Evaluate changes to equipment and processes and determine validation or requalification requirements.
Investigate validation deviations and support root-cause analysis and corrective actions.
Apply risk-based approaches to validation and qualification activities.
Maintain clear, accurate and inspection-ready GMP documentation.
Support internal audits and regulatory inspections.
Identify opportunities to simplify, standardize and continuously improve validation processes.
What You’ll Bring
Minimum Qualifications
Bachelor’s degree in Engineering, Life Sciences or a related technical discipline.
1–2 years of experience in validation, engineering, manufacturing, quality or another relevant technical environment (internship experience included)
Experience working in, or exposure to, a regulated or quality-driven manufacturing environment.
Strong technical writing, problem-solving and communication skills.
Ability to work effectively with cross-functional teams.
Experience That Will Help You Succeed
Relevant experience in one or more of these areas is valuable but not required:
IQ/OQ/PQ or process validation.
Equipment, facility or utility qualification.
HVAC, purified water, compressed air or manufacturing equipment.
GMP manufacturing and quality systems.
Change control, deviations, root-cause investigations or CAPA.
Risk-based validation approaches such as FMEA or ASTM E2500.
GAMP 5 and computerized system validation.
Engineering or capital-project execution.
Lean Manufacturing, PPI or other continuous-improvement methodologies.
Regulatory inspection or audit support.
What Makes This Opportunity Stand Out:
Our total rewards offering includes competitive compensation, an annual incentive opportunity, healthcare benefits and a range of employee benefits, along with opportunities for professional development and career growth.
Build valuable technical expertise.
Develop hands-on experience across equipment qualification, utilities, facilities, manufacturing processes and GMP validation.
Work on meaningful projects.
Support new equipment, facility improvements and manufacturing initiatives from startup through qualification.
Learn across functions.
Partner with experienced colleagues across Engineering, Quality, Manufacturing, Automation and Maintenance.
Grow your career.
Build skills in validation, engineering, quality systems, project execution and continuous improvement within a global science and technology organization.
Make an impact.
Your work helps maintain reliable manufacturing operations and the quality systems that support products used by customers around the world.
Compensation and Benefits
The salary range estimated for this position based in New York is $70,000.00–$86,000.00.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
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)Job Description
Validation Engineer II
Grand Island, NY | On-site - Relocation assistance is not available.
Candidates must be legally authorized to work in the United States without sponsorship.
Employment is contingent upon successful completion of applicable pre-employment requirements, including a background check and drug screening.
Build Your Career in Validation. Make an Impact That Matters.
At Thermo Fisher Scientific, your engineering work helps enable our customers to make the world healthier, cleaner and safer.
We are looking for a Validation Engineer II to join our Grand Island manufacturing team. This is an excellent opportunity for an early-career engineer or validation professional who wants to build valuable experience in GMP manufacturing, equipment and facility qualification, process validation, capital projects and continuous improvement.
You’ll work directly with Engineering, Manufacturing, Quality, Maintenance and Automation teams and gain hands-on exposure to projects that have a meaningful impact on our operations and the customers we serve.
What You’ll Do
As a Validation Engineer II, you will help ensure our manufacturing equipment, facilities, utilities and processes operate reliably and meet applicable quality and regulatory requirements.
You will:
Develop and execute validation and qualification activities for manufacturing equipment, facilities, utilities and processes.
Author and execute IQ, OQ and PQ protocols, validation plans and summary reports.
Support the commissioning, startup and qualification of new equipment and facility improvements.
Partner with Engineering, Manufacturing, Quality, Maintenance and Automation teams to solve technical problems and successfully deliver projects.
Evaluate changes to equipment and processes and determine validation or requalification requirements.
Investigate validation deviations and support root-cause analysis and corrective actions.
Apply risk-based approaches to validation and qualification activities.
Maintain clear, accurate and inspection-ready GMP documentation.
Support internal audits and regulatory inspections.
Identify opportunities to simplify, standardize and continuously improve validation processes.
What You’ll Bring
Minimum Qualifications
Bachelor’s degree in Engineering, Life Sciences or a related technical discipline.
1–2 years of experience in validation, engineering, manufacturing, quality or another relevant technical environment (internship experience included)
Experience working in, or exposure to, a regulated or quality-driven manufacturing environment.
Strong technical writing, problem-solving and communication skills.
Ability to work effectively with cross-functional teams.
Experience That Will Help You Succeed
Relevant experience in one or more of these areas is valuable but not required:
IQ/OQ/PQ or process validation.
Equipment, facility or utility qualification.
HVAC, purified water, compressed air or manufacturing equipment.
GMP manufacturing and quality systems.
Change control, deviations, root-cause investigations or CAPA.
Risk-based validation approaches such as FMEA or ASTM E2500.
GAMP 5 and computerized system validation.
Engineering or capital-project execution.
Lean Manufacturing, PPI or other continuous-improvement methodologies.
Regulatory inspection or audit support.
What Makes This Opportunity Stand Out:
Our total rewards offering includes competitive compensation, an annual incentive opportunity, healthcare benefits and a range of employee benefits, along with opportunities for professional development and career growth.
Build valuable technical expertise.
Develop hands-on experience across equipment qualification, utilities, facilities, manufacturing processes and GMP validation.
Work on meaningful projects.
Support new equipment, facility improvements and manufacturing initiatives from startup through qualification.
Learn across functions.
Partner with experienced colleagues across Engineering, Quality, Manufacturing, Automation and Maintenance.
Grow your career.
Build skills in validation, engineering, quality systems, project execution and continuous improvement within a global science and technology organization.
Make an impact.
Your work helps maintain reliable manufacturing operations and the quality systems that support products used by customers around the world.
Compensation and Benefits
The salary range estimated for this position based in New York is $70,000.00–$86,000.00.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
See All 9 Validation Engineer Jobs in New York
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Find Validation Engineer JobsValidation Engineer Jobs by City in New York
Where New York roles are concentrated, by current openings.
Validation Engineer Job Market in New York
A snapshot from current New York openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Consulting & Professional Services
- Biotechnology & Pharmaceuticals
What New York Employers Look For
The qualifications that appear most often in validation engineer jobs across New York.
- Bachelor's degree in engineering, life sciences, or a closely related technical discipline
- Hands-on experience with FDA validation protocols including IQ, OQ, and PQ documentation
- Familiarity with 21 CFR Part 11, GMP, and cGMP regulatory frameworks as applied in New York facilities
- Proficiency writing and executing validation master plans, protocols, and summary reports
- Experience with computer system validation and electronic batch records in regulated environments
- Strong working knowledge of risk assessment tools such as FMEA and change control procedures
Validation Engineer Jobs in New York: Frequently Asked Questions
How do you become a validation engineer in New York?
The standard path into validation engineering in New York starts with a bachelor's degree in chemical, mechanical, pharmaceutical, or biomedical engineering, or a life sciences field. No state-issued license is required for the role itself, but employers across New York's biopharma and medical device sectors expect candidates to demonstrate working knowledge of FDA regulations and GMP principles. Professional certifications such as the ASQ Certified Quality Engineer credential are widely recognized and strengthen a candidate's profile with regulated-industry employers in the state.
Which companies hire validation engineers in New York?
Employers hiring validation engineers in New York right now include Katalyst Healthcares & Life Sciences, Aldevron, and Marquardt, based on current listings on Migrate Mate as of August 2026. New York's dense concentration of FDA-regulated pharmaceutical, biotechnology, and medical device manufacturers means steady, year-round demand for qualified validation professionals at both large corporations and specialized contract manufacturing organizations.
Which New York cities have the most validation engineer jobs?
The cities with the most validation engineer openings in New York are Rochester, New York, and Cazenovia. New York City anchors demand through its large hospital systems and life sciences firms, while Long Island's established pharmaceutical and biotech manufacturing corridor drives strong hiring in suburban markets, and the Hudson Valley reflects Regeneron's substantial presence and the cluster of contract manufacturers that have grown around it.
Are there remote validation engineer jobs in New York?
Yes, but they're rare. Validation engineering is fundamentally a hands-on, on-site discipline requiring direct interaction with equipment, systems, and manufacturing environments, so most roles in New York require physical presence. About 33% of validation engineer openings tied to New York are remote or hybrid as of August 2026. The portions of the role most amenable to remote work are documentation writing, protocol authoring, and computer system validation activities that do not require physical equipment access.
How can I get hired as a validation engineer in New York with little or no experience?
The most realistic entry path is a junior or associate validation engineer role at a contract manufacturing organization or a large pharmaceutical employer in New York's Long Island or Hudson Valley markets, where structured onboarding programs bring in recent graduates. Lateral moves from quality assurance, laboratory technician, or manufacturing operations roles within the same facility are common and well-regarded. Completing a validation-focused certificate program and earning the ASQ Certified Quality Technician credential strengthens an application and signals readiness for regulated-industry work to New York employers.
Where can I find and apply to validation engineer jobs in New York?
You can find and apply to validation engineer jobs in New York on Migrate Mate, which lists current openings tied to New York employers and facilities. Review the roles available, identify the ones that match your experience and target location, and apply directly to the positions that fit.
See All 9 Validation Engineer Jobs in New York
Find roles in New York that match your experience and apply in just a few clicks.
Find Validation Engineer Jobs