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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Job Summary
Validates and revalidates new or modified products, equipment or systems. Provides technical support to Operations in terms of equipment/system initial validation and equipment/system requalifications.Salary Range: $60,966-$85,694 annually
Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities.
Responsibilities
- Performs equipment requalifications per Standard Operating Procedures (SOPs). Coordinates and communicates all testing with affected functional groups and evaluates test results. Analyzes data, composes a Final Report and circulates for approval.
- Executes equipment validation studies per SOPs or utilizing reference templates, to include protocol preparation, scheduling, protocol execution, data analysis, Final Report preparation and circulation for approval.
- Programs and operates department analytical instruments (such as temperature/humidity dataloggers and thermocouples) to perform controlled temperature/humidity chamber qualifications/requalifications (i.e.: lyophilizers, sterilizers, depyrogenation ovens/tunnels, warehouses, coolers/freezers, incubators, etc.).
- Participates in improvements to validation programs/procedures as needed to remain current with cGMPs and industry standards.
- Participates in teams assembled to validate and maintain systems and equipment.
- Participates in deviation investigations and corrective and/or preventative actions (CA/PA).
- Performs HEPA Filter integrity/velocity testing and participates in Critical Area (Class 100) airflow pattern testing. Programs and operates test equipment such as smoke generators, photometers, velocity meters, etc., and accurately records and evaluates results.
- Participates in presentation for Regulatory Agency(s) when necessary.
- Participates in equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control.
Requirements
- BS/BA degree in science, engineering, manufacturing technology or closely related field, or equivalent experience in a manufacturing facility.
- 1 – 3 years pharmaceutical manufacturing experience.
- Excellent attention to detail.
- Must be proactive, ability to work in high performance teams, strong interpersonal and self-management skills.
- Must be able to interact with varying levels within the company.
- Ability to work both independently and in partnership with others; ability to use initiative and drive to achieve results.
- Ability to write reports, deviations or other technical documents clearly, concisely, and accurately; accurately record data and a basic understanding of statistical analysis.
- PC literate with standard office application (Word, Excel, PowerPoint, Project, Access) competency.
- Knowledge and understanding of cGMPs, industry guidance, and aseptic techniques.
- The Company’s primary business language is English. The successful candidate must be able to effectively speak, read, write, and understand English to perform the essential functions of the position, including independently understanding policies, procedures, training materials, and workplace communications written in English due to our heavily regulated work environment.
Additional Information
We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability, 401K with company contribution, and wellness program.
Please note that joining our team does not create a guaranteed or permanent employment arrangement. All employment is at‑will, meaning both the employee and Fresenius Kabi have the right to end the employment relationship at any time, in accordance with applicable federal and state laws.
Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.
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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
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
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, Marquardt, and GalaxyPharma, based on current listings on Migrate Mate as of September 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 Albany. 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 20% of validation engineer openings tied to New York are remote or hybrid as of September 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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