
GMP Technician I
New York, NYFull-time$26.98–30.82/hrSeen 2w agoSeen in employer's feed 3 days ago
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At a glance
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Requirements
Credentials this posting asks for.
Job overview
The GMP Technician I manufactures gene therapy products and performs quality control testing in the Belfer Gene Therapy Core. The role follows facility quality systems and FDA and/or EU Good Manufacturing Practice standards for early drug development. It also supports process validation and development, documentation, environmental monitoring, and cleanroom operations.
Skills & qualifications
Skills
Qualifications
Full job description
Title: GMP Technician I
Location: Upper East Side
Org Unit: Belfer Gene Therapy Core
Work Days: Monday-Friday
Weekly Hours: 35.00
Exemption Status: Non-Exempt
Salary Range: $26.98 - $30.82
*As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices
Position Summary
Responsible for manufacturing and performing quality control (QC) tests of gene therapy products in compliance with the quality system established in the Belfer Gene Therapy Core Facility and the FDA and/or EU Good Manufacturing Practice Standards for early drug development phase.
Job Responsibilities
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Manufactures AAV and Adenovirus based gene therapy products in cleanrooms following GMP. Procedures include reagents and media preparation, cell cuture and virus purification using filtration, gradient and/or chromatography methods, and aseptic filling.
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Completes required processing documentation, including Product Data Records (PDRs), Nonconformance Reports, Change Control, CAPA etc. following the Standard Operating Procedures (SOPs) for GMP documentation.
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Performs Quality Control (QC) testings using techniques of molecular biology and biochemistry.
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Drafts and revises Standard Operating Procedures (SOPs) and Production Data records (PDRs).
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Participates in equipment qualification (EQ) and process validation.
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Participates in GMP process development and process transfer activities. Prepares and maintains detailed records, logs and summary reports of all procedures and results.
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Performs environment monitoring.
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Participates in production room sanitization.
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Attends GMP meetings and training programs and other institutional meetings and training programs. Conducts library research and literature searches. Keeps abreast of scientific literature and new developments in laboratory products.
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Performs other related duties as assigned.
Education
- Bachelor's Degree
Experience
Bachelor's degree in Science, preferably with biology, bioengineering, and biochemistry majors.
Prior related experience.
Knowledge, Skills and Abilities
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Excellent communication skills (both verbal and written).
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Demonstrated organizational skills and ability to pay close attention to detail.
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Ability to meet multiple deadlines and handle multiple priorities.
Licenses and Certifications
Working Conditions/Physical Demands
Should feel comfortable working in a cleanroom wearing an overall gown including facemask and goggles.
Cornell welcomes students, faculty, and staff with diverse backgrounds from across the globe to pursue world-class education and career opportunities, to further the founding principle of “any person, any study.” No person shall be denied employment on the basis of any legally protected status or subjected to prohibited discrimination involving, but not limited to, such factors as race, ethnic or national origin, citizenship and immigration status, color, sex, pregnancy or pregnancy-related conditions, age, creed, religion, arrest and/or conviction record, military or veteran status, sexual orientation, gender expression and/or identity, an individual’s genetic information, domestic violence victim status, familial status, marital status, or any other characteristic protected by applicable federal, state, or local law.
Cornell University embraces diversity in its workforce and seeks job candidates who will contribute to a climate that supports students, faculty, and staff of all identities and backgrounds. We hire based on merit, and encourage people from historically underrepresented and/or marginalized identities to apply. Consistent with federal law, Cornell engages in affirmative action in employment for qualified protected veterans as defined in the Vietnam Era Veterans’ Readjustment Assistance Act (VEVRRA). We also recognize a lawful preference in employment practices for Native Americans living on or near Indian reservations in accordance with applicable law.
How this job compares
Set against the 1,431 open Quality Control jobs on Olive Jobs, counted November 6, 2026.
- Pay
- This posting$26.98–30.82/hr
- New York median$24–29/hr54 hourly ranges
- US median$24–29/hr451 hourly ranges
This range's midpoint, $28.90/hr, is 6% above the New York median midpoint ($27/hr) — in the middle half of Quality Control hourly ranges in New York.
- Openings
- Olive Jobs lists 108 open Quality Control jobs in New York and 1,431 across the US. Under 1% of them nationwide are listed as remote or flexible.
- Hiring the most in New York
- Regeneron Pharmaceuticals12 open
- Curia8 open
- Eurofins6 open
- Experience
- Quality Control postings that state a minimum ask for 3 years of experience at the median; the middle half ask for 2 to 5 years (992 postings).
- Education
- This posting asks for a bachelor's degree; 341 of the 1,431 open Quality Control jobs (24%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 6, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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