New · posted Nov 4
Regeneron · Biotechnology
Quality Control Analyst
- Rensselaer, NY
- On-site
- Full-time
- Associate & Specialist
The role
Build our future together
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently looking for a Quality Control (QC) Analyst to join our Biochemistry Gels Team. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. The QC Analyst will be part of the lot release for market use of our products. They will perform a variety of biochemical analyses on products, in-process materials or stability samples in support of the company’s quality programs.
As a QC Analyst, a typical day might include the following
- Develop and maintain efficient processes to support commercial testing in laboratory functions. Examples include management of materials, reagents, equipment, electronic systems, documents, laboratory safety and inspection readiness.
- Conduct testing on in-process, product, stability and/or research samples.
- Complete and/or coordinate the completion of lab operations activities.
- Ensure timely completion of activities impacting the QC commercial operations.
- Review test results to ensure compliance with standards; report any quality anomalies.
- Perform laboratory OOT, atypical and OOS investigations.
- Writes and revise control test procedures and SOPs.
- Conduct efforts to continuously improve processes while maintaining GxP compliance and keeping tasks on track.
- May be responsible for maintaining a specific project.
- May devise and develop new analytical methods and techniques.
- May assist in validation of methods.
- May be involved in establishing the transfer of methodology from R&D.
This role might be for you if you:
- Maintain integrity and honesty at all times.
- Enjoy working independently and as part of a team.
- Thrive in a fast-paced setting where your priorities can quickly change based on the needs of the business and our patients.
- Have effective time management skills to work on multiple projects.
- Have strong social skills.
- Have excellent written and verbal communication skills
What you need
This role requires
- Bachelor of Science or Bachelor of Arts in Life Sciences or related field, or a degree in Biotechnology/Biological Science, or an equivalent combination of education and experience. Level is settled based on qualifications relevant to the role.
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.
Pay and benefits
$51,501 – $80,496 a year
Employer provided$24.76 – $38.70 an hour · yearly at 2,080 hours (40 a week)
How this comparesSalary Range (hourly)
$24.76 - $38.70
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
Rensselaer, NYOn-siteOpen in Maps (opens in a new tab)
More jobs in Rensselaer, NYWorking conditions
When & where
- Location: Rensselaer, New York, United States
- Work model: 1st shift | Monday-Friday, 8am-4:30pm
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 · November 4, 2026
Salary intelligence
How the pay compares
This role's midpoint is 10% below the US median for Quality Control roles at this level.
This roleEmployer provided
Associate & Specialist roles in New York22 roles publishing pay
Associate & Specialist roles in the US79 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $51,501 | — | $80,496 |
| New York (middle half) | $58,000 | $66,000 | $75,750 |
| All US (middle half) | $59,250 | $73,000 | $88,250 |
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, November 4, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 242 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 25 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods9
- GMP and compliance3
- Documentation and SOPs3
- Collaboration and leadership3
- Investigations and CAPA1
- Validation and qualification1
- Data and digital systems1
- Clinical trial conduct1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Control work in biotechnology, led by the one this posting names, each linked to the agency or standards body that publishes it.
- FDAFDA OOS guidance(official source, opens in a new tab)Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical ProductionNamed in the posting
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticals
- USPUSP–NF(official source, opens in a new tab)US Pharmacopeia general chapters and monographs, such as <61> bioburden, <85> endotoxin, <1225> validation
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and Answers
- ICHICH Q2(R2) and Q14(official source, opens in a new tab)Validation and development of analytical procedures
- FDAFDA analytical procedures guidance(official source, opens in a new tab)Analytical Procedures and Methods Validation for Drugs and Biologics
- ICHICH Q1 stability testing(official source, opens in a new tab)Stability testing of drug substances and drug products
- FDA21 CFR Parts 600 to 680(official source, opens in a new tab)FDA standards for biological products, from licensing to lot release
- ICHICH Q5 and Q6B(official source, opens in a new tab)Quality of biotechnological products and their specifications
- FDAFDA Investigations Operations Manual(official source, opens in a new tab)How FDA investigators plan and conduct inspections
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- EDQMEuropean Pharmacopoeia(official source, opens in a new tab)The Ph. Eur. quality standards for medicines in Europe, published by the EDQM
- ICHICH Q3 impurities(official source, opens in a new tab)Impurities in drug substances and products, residual solvents and elemental impurities
- FDAFDA aseptic processing guidance(official source, opens in a new tab)Sterile Drug Products Produced by Aseptic Processing: Current Good Manufacturing Practice
- ISOISO 14644-1(official source, opens in a new tab)Cleanroom air cleanliness classification by particle concentration
- EUEU GMP (EudraLex Volume 4)(official source, opens in a new tab)The EU's good manufacturing practice rules, including Annex 1 sterile and Annex 15 validation
Company hiring pulse
Regeneron on Regulatory Jobs
- 169
- Open roles
- 144
- Distinct roles
- 11
- Locations
By discipline
- Clinical71 42%
- Quality70 41%
- Regulatory28 17%
By level
- Associate & Specialist56 33%
- Director50 30%
- Manager48 28%
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Quality Control Analyst at Regeneron
Open until filled. $52K–$80K a year, employer provided.