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New · posted Oct 16

Regeneron · Biotechnology

Principal Quality Assurance Validation Specialist

  • Saratoga Springs, NY
  • On-site
  • Full-time
  • Senior & Principal
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EmploymentFull-time
Deadline

Open until filled

The role

Build our future together

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are hiring multiple Quality Assurance (QA) Validation Specialists to join our team at our new highly automated drug substance manufacturing facility in Saratoga Springs. This position validates and qualifies laboratory and analytical equipment in accordance with regulatory requirements, with secondary support for manufacturing equipment and utility validation in a highly automated, digitally integrated biologics environment. This role may have direct reports in the future.

What you need

This role requires

  • BS/BA in Engineering, Chemistry, or Life Sciences, may substitute relevant experience for education
    • Principal QA Validation Specialist: 8+ years of relevant experience
    • Staff QA Validation Specialist: 10+ years of relevant experience
    • Level will be determined based on experience
  • Previous people leadership/supervisory experience preferred
  • Experience with laboratory or analytical instrumentation (e.g., HPLC, GC, balances, spectrophotometers) in a GMP environment is preferred

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

  1. Generates, executes, and/or reviews master and completed qualification and validation protocols, summary reports, and associated data for laboratory and analytical equipment (e.g., HPLC, GC, balances, spectrophotometers, incubators) for conformance to regulations, SOPs, specifications, and other applicable acceptance criteria
  2. Analyzes the results of testing and determines the acceptability of results against pre-determined criteria
  3. Investigates and troubleshoots problems which occur with laboratory equipment and determines solutions or recommendations for changes and/or improvements
  4. Reviews, edits, and approves deviation notifications, deviation investigations, and corrective actions
  5. Reviews, edits, and approves change controls, SOPs, reports, and other documentation
  6. Provides secondary support for qualification of manufacturing equipment and utilities as needed
  7. Coordinates with Quality Control, Manufacturing Science, and outside contractors/vendors, including Automation and Computer Systems Assurance, to complete validation tasks for a highly automated facility
  8. Trains, advises and mentors teammate as needed
  9. May manage full-time employees as well as contractors
  10. Manages projects and prepares status reports
  11. Other duties assigned by management

Pay and benefits

$92,200 – $176,000 a year

Employer provided
How this compares

$92,200.00 - $176,000.00

  • 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

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

More jobs in Saratoga Springs, NY

Working conditions

The environment and physical rhythms of the role

  • Gowning: Full cleanroom attire (examples may include laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)
  • Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire

When & where

  • Location:
    • Initial: Rensselaer, New York, United States
    • Permanent: Saratoga Springs, New York, United States
  • Work model: Monday-Friday, 8am-4:30pm
    • Other requirements: Occasional flexibility may be requested for on-call schedule/weekend work
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 16, 2026

Salary intelligence

How the pay compares

This role's midpoint is 11% above the US median for Validation & CQV roles at this level.

This roleEmployer provided

$92,200 to $176,000 a year

Senior & Principal roles in the US47 roles publishing pay

Middle half $108,000 to $132,500, median $121,000
Annual base pay
Annual base payLowMedianHigh
This role$92,200—$176,000
All US$108,000$121,000$132,500

This role: Regeneron's own published range. Comparisons: the base pay employers published on open Validation & CQV roles at the same level on Regulatory Jobs, October 16, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Validation & CQV

The general path across 117 open Validation & CQV roles on Regulatory Jobs, with the titles they carry most. Not Regeneron's own promotion track.

  1. One step back

    Associate & Specialist

    Often: Associate QA Validation Specialist · Engineer II, Validation

    $77K median29 open
  2. This role

    Senior & Principal

    Often: Engineer III, Validation · Senior Engineer, Validation

    $121K median65 open
  3. Next step

    Manager

    Often: Validation Manager · Manager Quality Assurance Validation

    $141K median16 open
  4. Later

    Director

    Often: Associate Director, Validation · Associate Director, Computer Systems Assurance

  5. Later

    VP & Executive

    Often: Head of Validation & Risk Management

Skills DNA

What this role leans on

How many of the posting's 19 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 2 linesLab testing and methods: 5 linesDocumentation and SOPs: 4 linesInvestigations and CAPA: 2 linesValidation and qualification: 5 linesQuality systems and risk: 1 lineData and digital systems: 1 lineCollaboration and leadership: 3 linesGMPLab testingDocumentationInvestigationsValidationQuality systemsData systemsTeamwork
  • Lab testing and methods5
  • Validation and qualification5
  • Documentation and SOPs4
  • Collaboration and leadership3
  • GMP and compliance2
  • Investigations and CAPA2
  • Quality systems and risk1
  • Data and digital systems1

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.

Company hiring pulse

Regeneron on Regulatory Jobs

64
Open roles
54
Distinct roles
9
Locations

By discipline

  • Quality41 64%
  • Regulatory20 31%
  • Compliance & Safety3 5%

By level

  • Associate & Specialist31 48%
  • Manager20 31%
  • Director7 11%
See all 64 Regeneron roles

More roles at Regeneron

All 64 Regeneron roles

Similar Validation & CQV roles elsewhere

Principal Quality Assurance Validation Specialist at Regeneron

Open until filled. $92K–$176K a year, employer provided.

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