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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See related jobsSUMMARY OF POSITION
Author and provide input to critical Validation systems and conduct validation assessments of equipment, Facilities, and process systems. Compile and analyze data, prepare protocols, reports, and make recommendations for changes/or improvements. A primary resource for Periodic Equipment review systems. In addition, provide secondary/Backup support for Packaging Validation, Computer System Validation, Equipment and Instrumentation qualification, Facility, and Utility qualification.
ORGANIZATION STRUCTURE
The Validation Engineer reports directly to the Sr. Director Operations & Pharmaceutical Technology.
RESPONSIBILITIES
Primary responsibilities of this role include the following:
System/Process:
- Provide primary coverage on Equipment and Instrumentation Qualification- write, review, approve commissioning/qualification documentation. Provide Oversite and guidance on the program to maintain consistency and standards.
- Provide primary coverage on Facility and Utility Qualification- write, review, approve commissioning/qualification documentation. Provide Oversite and guidance on the program to maintain consistency and standards.
- Manage the periodic review of validated systems, equipment, and Utilities. Maintaining the system and organizing the assessment process.
- Represent/Support the Department in audits or regulatory inspections fielding questions related to the above systems and programs.
- Facilitate and/or support validation training on the above systems.
- Provide Backup Coverage for Packaging Validation.
- Co-Own and provide input to the Validation Master Plans for the Site, Computer System Validation, Equipment, Laboratory Instrumentation, Facility, and Utility Qualifications.
- Provide backup coverage on Computer System Validation performing Electronic records and Electronic Signature assessments, lead and assess risk assessments, evaluate supplier assessments, write, review, approve associated documentation.
- Provide Annual Product Review (APR) Support specific to Validation and Change Control as needed.
Documentation:
- Author Qualification and Validation Documents
- Edit and approve associated documentation
- Author APR supporting documents
- Author Periodic Review of validated systems documentation
- Author related Change Controls for systems and processes
QUALIFICATIONS
Bachelor’s Degree in science or Engineering Field of study
A minimum requirement of 3 years related Pharmaceutical experience- preference for Pharmaceutical Manufacturing Equipment Engineering and Validation experience.
This role requires technical writing and communication skills, the ability to understand and interpret technical documentation and a proficiency with a currently supported version of MS Excel and Word. The ability to handle multiple priorities is necessary for success.
GMP DECISION-MAKING AUTHORITY
- Inputs/Edits Validation and Qualification documentation- serves as resource in the development and approval of documentation.
- The technical approver for protocols and executed qualifications.
- Subject Matter Expert approver for related Change Controls.
The anticipated base salary range for this position is $75,000 to $83,000. This position is eligible for Alvogen’s annual discretionary bonus and comprehensive benefits package, consisting of medical and prescription drug coverage (two PPO plans and an HDHP with Health Savings Account and employer contribution), dental, vision, flexible spending accounts. Alvogen’s benefits package also includes a retirement savings program, long-term care coverage, paid time off (176 hours to start) inclusive of sick time, disability benefits, life insurance, a wellness program, and 13 company recognized paid holidays per year. We anticipate this position will be posted on 11/10/2026 and remain open for at least 30 days. To apply, select the apply button and submit your application.
“An Equal Opportunity Employer, including disability/vets.”
SUMMARY OF POSITION
Author and provide input to critical Validation systems and conduct validation assessments of equipment, Facilities, and process systems. Compile and analyze data, prepare protocols, reports, and make recommendations for changes/or improvements. A primary resource for Periodic Equipment review systems. In addition, provide secondary/Backup support for Packaging Validation, Computer System Validation, Equipment and Instrumentation qualification, Facility, and Utility qualification.
ORGANIZATION STRUCTURE
The Validation Engineer reports directly to the Sr. Director Operations & Pharmaceutical Technology.
RESPONSIBILITIES
Primary responsibilities of this role include the following:
System/Process:
- Provide primary coverage on Equipment and Instrumentation Qualification- write, review, approve commissioning/qualification documentation. Provide Oversite and guidance on the program to maintain consistency and standards.
- Provide primary coverage on Facility and Utility Qualification- write, review, approve commissioning/qualification documentation. Provide Oversite and guidance on the program to maintain consistency and standards.
- Manage the periodic review of validated systems, equipment, and Utilities. Maintaining the system and organizing the assessment process.
- Represent/Support the Department in audits or regulatory inspections fielding questions related to the above systems and programs.
- Facilitate and/or support validation training on the above systems.
- Provide Backup Coverage for Packaging Validation.
- Co-Own and provide input to the Validation Master Plans for the Site, Computer System Validation, Equipment, Laboratory Instrumentation, Facility, and Utility Qualifications.
- Provide backup coverage on Computer System Validation performing Electronic records and Electronic Signature assessments, lead and assess risk assessments, evaluate supplier assessments, write, review, approve associated documentation.
- Provide Annual Product Review (APR) Support specific to Validation and Change Control as needed.
Documentation:
- Author Qualification and Validation Documents
- Edit and approve associated documentation
- Author APR supporting documents
- Author Periodic Review of validated systems documentation
- Author related Change Controls for systems and processes
QUALIFICATIONS
Bachelor’s Degree in science or Engineering Field of study
A minimum requirement of 3 years related Pharmaceutical experience- preference for Pharmaceutical Manufacturing Equipment Engineering and Validation experience.
This role requires technical writing and communication skills, the ability to understand and interpret technical documentation and a proficiency with a currently supported version of MS Excel and Word. The ability to handle multiple priorities is necessary for success.
GMP DECISION-MAKING AUTHORITY
- Inputs/Edits Validation and Qualification documentation- serves as resource in the development and approval of documentation.
- The technical approver for protocols and executed qualifications.
- Subject Matter Expert approver for related Change Controls.
The anticipated base salary range for this position is $75,000 to $83,000. This position is eligible for Alvogen’s annual discretionary bonus and comprehensive benefits package, consisting of medical and prescription drug coverage (two PPO plans and an HDHP with Health Savings Account and employer contribution), dental, vision, flexible spending accounts. Alvogen’s benefits package also includes a retirement savings program, long-term care coverage, paid time off (176 hours to start) inclusive of sick time, disability benefits, life insurance, a wellness program, and 13 company recognized paid holidays per year. We anticipate this position will be posted on 11/10/2026 and remain open for at least 30 days. To apply, select the apply button and submit your application.
“An Equal Opportunity Employer, including disability/vets.”
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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 Aldevron, Voyant Photonics, and Stark Pharma Solutions, based on current listings on Migrate Mate as of November 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 New York, Rochester, and Norwich. 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 50% of validation engineer openings tied to New York are remote or hybrid as of November 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.
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