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New · posted Nov 6

Regeneron · Biotechnology

QC External Lab Coordinator

  • Rensselaer, NY
  • On-site
  • Full-time
  • Associate & Specialist
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EmploymentFull-time
DeadlineOpen until filled

About the job

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are currently looking to fill a Quality Control (QC) External Lab Coordinator position. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our QC External Testing Coordinators supports the daily operations of the QC External Testing group in accordance with Standard Operating Procedures (SOPs) and cGMP regulations.

When & where:

  • Location: Rensselaer, New York, United States
  • Work model: 1st shift | Monday-Friday | 8:00am-4:30pm

Discover your role:

  • Serving as the primary operational liaison between Contract Testing Laboratories (CTLs) and internal partners, including QC, QA, Regulatory Affairs, Manufacturing, and Supply Chain teams.
  • Leading cross-functional meetings with CTLs and internal partners to establish project timelines, discuss technical issues, supervise progress, and drive issue resolution.
  • Monitoring CTL performance metrics, turnaround times, testing capacity, and schedule adherence; growing risks and implementing mitigation plans as appropriate.
  • Using a sample tracking system (LIMS) to review sample inventory against samples sent and received by external laboratories to resolve accuracy and to maintain sample integrity.
  • Coordinating activities between external laboratories and Regeneron subject matter experts (SMEs) to troubleshoot issues and identify root causes.
  • Coordinating on-time shipment of samples to Contract Testing Labs.
  • Coordinating receipt and entry of test data from Contract Testing Labs.
  • Providing technical support as needed for invalid assays, deviations, OOS/OOT investigations.
  • Initiating and completing CAPAs and Change Controls in accordance with site procedures.
  • Writing new SOPs and updating existing SOPs as needed.
  • Initiating and handling workflows in the electronic document management system.
  • Ensuring that all work performed follows required regulatory requirements (e.g. cGMP), company policies, and standard operating procedures (SOPs).
  • Proactively identifying and implementing process improvements, lean initiatives.
  • Performing other duties relevant to the position as required.

This role requires:

  • Bachelor's degree in a scientific field (Biology, Chemistry, Microbiology, or related field)
  • Experience with cGMP is preferred.
  • Occasions where you may be required to be on call during off-hours (ex. weekends, holiday breaks) to support critical shipment or entry of results.
  • Level is settled based on qualifications relevant to the role.

Does this sound like you?  Apply now to take your first steps toward living the Regeneron Way!  We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for employees at all levels!

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, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or maternity status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations.  We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process.  Please contact us to discuss any accommodations you think you may need.


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.

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.

Salary Range (hourly)

$25.24 - $39.47

Pay and benefits

$52,499 – $82,098 a year

Employer provided

$25.24 – $39.47 an hour · yearly at 2,080 hours (40 a week)

How this compares
  • Health and wellness programs

  • Fitness centers

  • Stock

  • 401(k) company match

  • Insurance benefits (medical, dental, vision, life, disability)

  • Paid time off

Where you'll work

Rensselaer, NYOn-siteOpen in Maps (opens in a new tab)

More jobs in Rensselaer, NY

Job intelligence

The context around this role

Live data · November 6, 2026

Salary intelligence

How the pay compares

This role's midpoint is 8% below the US median for Quality Control roles at this level.

This roleEmployer provided

$52,499 to $82,098 a year

Associate & Specialist roles in New York23 roles publishing pay

Middle half $58,000 to $74,500, median $66,000

Associate & Specialist roles in the US84 roles publishing pay

Middle half $61,500 to $90,125, median $73,500
Annual base pay
Annual base payLowMedianHigh
This role$52,499—$82,098
New York$58,000$66,000$74,500
All US$61,500$73,500$90,125

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 6, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Control

The general path across 250 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Regeneron's own promotion track.

  1. This role

    Associate & Specialist

    Often: Quality Control Analyst · Specialist, Quality Control

    $74K median129 open
  2. Next step

    Senior & Principal

    Often: Scientist, Quality Control · Senior Scientist, Quality Control

    $96K median65 open
  3. Later

    Manager

    Often: Supervisor, Quality Control · Manager, Quality Control

    $112K median36 open
  4. Later

    Director

    Often: Associate Director, Quality Control · Senior Director, Quality Control

    $198K median20 open

Skills DNA

What this role leans on

How many of the posting's 29 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 3 linesLab testing and methods: 9 linesDocumentation and SOPs: 5 linesInvestigations and CAPA: 2 linesQuality systems and risk: 2 linesData and digital systems: 1 lineClinical trial conduct: 1 lineCollaboration and leadership: 2 linesGMPLab testingDocumentationInvestigationsQuality systemsData systemsClinical trialsTeamwork
  • Lab testing and methods9
  • Documentation and SOPs5
  • GMP and compliance3
  • Investigations and CAPA2
  • Quality systems and risk2
  • Collaboration and leadership2
  • 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 two this posting names, each linked to the agency or standards body that publishes it.

Company hiring pulse

Regeneron on Regulatory Jobs

177
Open roles
177
Distinct roles
11
Locations

By discipline

  • Quality75 42%
  • Clinical74 42%
  • Regulatory29 16%

By level

  • Associate & Specialist58 33%
  • Manager53 30%
  • Director52 29%
See all 177 Regeneron roles

More roles at Regeneron

All 177 Regeneron roles

Similar Quality Control roles elsewhere

QC External Lab Coordinator at Regeneron

Open until filled. $52K–$82K a year, employer provided.

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