

New · posted Oct 13
Regeneron · Biotechnology
Associate QA Validation Specialist
- United States
- On-site
- Full-time
- Associate & Specialist
Closes Nov 12, 2026 · 30 days left
The role
The QA Validation department is hiring! The QA Validation Specialist - validates and qualifies equipment, systems, and processes in accordance with regulatory requirements and support, follow and implement company manufacturing standards policies and procedures.
As a QA Validation Specialist, a typical day might include the following:
- Generates, implements and/or reviews master and completed qualification and validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria
- Analyzes the results of testing and determines the acceptability of results against pre-determined criteria.
- Investigates and troubleshoots problems which occur and determines solutions or recommendations for changes and/or improvements.
- Reviews, edits and approves deviation notifications, deviation investigations, corrective actions, change controls, SOPs, reports and other documentation
- Coordinates with other departments or outside contractors/vendors to complete validation tasks.
- May supervise, provide direction and assign work to Validations Specialists and/or contingent workers to meet goals and deadlines.
- Manages projects and prepares status reports.
- May present at both internal and external (regulatory) audits
- Other duties assigned by management.
- Some travel may be required.
This role may be for you if you:
- Ability to maintain integrity and honesty at all times
- Ability to work independently or as part of a team
- Ability to communicate with transparency
- Continuously drive to improve processes for improved performance
- Demonstrate supportive behavior at all times
- Basic working knowledge of Microsoft Suite (Word, Excel, Powerpoint)
- Gathers and organizes information
- Meets commitments on time
- Performs well-defined tasks
- Effective time management skills
- Seeks to identify continuous improvement needs
In order to be considered for this position, you must hold a BS/BA in Engineering, Chemistry, or Life Sciences and
- 0 – 2 years of relevant experience for an Associate
- 2+ years of relevant experience for a Specialist
- 5+ years of relevant experience for a Senior Specialist
- 8+ years of relevant experience for a Principal Specialist
- May substitute proven experience for education requirement
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 need
Pay and benefits
$62,355 – $92,400 a year
Employer provided$62,355.00 - $92,400.00
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
United StatesOn-siteOpen in Maps (opens in a new tab)
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 13, 2026
Salary intelligence
How the pay compares
This role's midpoint is 3% below the US median for Validation & CQV roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US11 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $62,355 | — | $92,400 |
| All US (middle half) | $76,000 | $80,000 | $91,250 |
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 13, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Validation & CQV
The general path across 99 open Validation & CQV 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 34 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Validation and qualification5
- Documentation and SOPs4
- GMP and compliance2
- Investigations and CAPA2
- Quality systems and risk2
- Collaboration and leadership2
- Lab testing and methods1
- Data and digital systems1
Company hiring pulse
Regeneron on Regulatory Jobs
- 38
- Open roles
- 35
- Distinct roles
- 9
- Locations
By discipline
- Quality25 66%
- Regulatory10 26%
- Compliance & Safety3 8%
By level
- Manager13 34%
- Associate & Specialist13 34%
- Director7 18%
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Associate QA Validation Specialist at Regeneron
Applications close November 12. $62K–$92K a year, employer provided.

