

New · posted Oct 19
Regeneron · Biotechnology
Associate Quality Control Analyst (Virology)
- East Greenbush, NY
- On-site
- Full-time
- Associate & Specialist
Open until filled
The role
Regeneron is looking for an Associate Quality Control Virology Analyst. In this role you will be responsible for sample chain of custody, sample processing, testing and test data reporting and archiving.
What you need
This role requires
A BS/BA in Cell Biology, Microbiology, Biochemistry, or related Science.
Experience working in a GMP virology or cell culture lab is strongly preferred.
Level to be determined based on qualifications.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.
What you'll do
Discover your role
- Ensure proper level of laboratory supplies and reagents and maintain laboratory in an audit readiness stage and cGMP compliant manner at all times.
- Perform routine and non-routine virus and mycoplasma testing (cell-based and molecular biology assays) of manufactured in-process commercial and clinical products according to cGMP and associated standard operating procedures.
- Review data for conformance to cGMP and specifications and assist with investigation of laboratory deviations.
- Collect, process and report on data for samples associated with in-process testing for the clinical and/or commercial manufacturing facilities.
- Apply basic and advanced troubleshooting methods.
- Serve as SME for an assigned assay.
- Assist in data trending, data review, and lab maintenance activities.
- Participate in non-routine projects.
- Can apply knowledge to assist in investigations and support studies and protocols.
- Have experience performing cell culture activities to support virus testing.
- Can be responsible for collecting, entering data and generating reports from electronic systems.
- Can apply knowledge to assist in investigations and support studies and protocols.
- ·Have experience performing cell culture activities to support virus testing· Can be responsible for collecting, entering data and generating reports from electronic systems· Always display good manufacturing practices and good laboratory practices.
Pay and benefits
$45,302 – $70,699 a year
Employer provided$21.78 – $33.99 an hour · yearly at 2,080 hours (40 a week)
How this comparesSalary Range (hourly)
$21.78 - $33.99
Annual bonuses or incentive plans
Equity awards
401(k) company match
Health and wellness programs
Medical, dental, vision, life and disability insurance
Paid time off
Where you'll work
East Greenbush, NYOn-siteOpen in Maps (opens in a new tab)
More jobs in East Greenbush, NYWorking conditions
When & where
- Monday–Friday, 8:00am–4:30pm
- Location: East Greenbush, New York, United States
Equal opportunity, accessibility and legal noticesRegeneron's statements, word for word
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
Job intelligence
The context around this role
Live data · October 20, 2026
Salary intelligence
How the pay compares
This role's midpoint is 2% below the US median for Quality Control roles at this level.
This roleEmployer provided
Associate & Specialist roles in New York18 roles publishing pay
Associate & Specialist roles in the US111 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $45,302 | — | $70,699 |
| New York (middle half) | $47,875 | $58,000 | $70,500 |
| All US (middle half) | $48,000 | $59,000 | $76,000 |
This role: Regeneron's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 20, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 306 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Regeneron's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 21 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods10
- Documentation and SOPs6
- GMP and compliance5
- Investigations and CAPA3
- Data and digital systems2
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticals
- FDA21 CFR Part 58 (GLP)(official source, opens in a new tab)Good laboratory practice for nonclinical laboratory studies
From Regulatory News
Manufacturing and quality coverage for this professionCompany hiring pulse
Regeneron on Regulatory Jobs
- 73
- Open roles
- 63
- Distinct roles
- 9
- Locations
By discipline
- Quality51 70%
- Regulatory19 26%
- Compliance & Safety3 4%
By level
- Associate & Specialist36 49%
- Manager21 29%
- Senior & Principal9 12%
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Associate Quality Control Analyst (Virology) at Regeneron
Open until filled. $45K–$71K a year, employer provided.

