Temporary-Quality Reviewer / Batch Release Specialist

Regeneron Pharmaceuticals, Inc.; City of Troy (NY); Híbrido; USD 70.000 - 95.000; Jornada completa

Descripción de la vacante

Regeneron Pharmaceuticals, Inc. is seeking a Quality Reviewer / Batch Release Specialist to verify batch records and CoAs for clinical and commercial products.

You will work with regulatory leads, global teams, and distribution compliance to ensure product quality and regulatory compliance across the portfolio. The role supports QP certification processes and country-specific release requirements, with a 6‑month contract and a flexible work model including remote and on-site options at

Formación

• Bachelor’s degree required with life sciences focus.
• 2+ years in pharmaceutical/biotech QA/QC or regulatory affairs.
• Experience with GMP, batch records, and lot release.

Responsabilidades

• Review batch status forms and CoAs to confirm lot disposition and expiry.
• Cross-check release testing panels against specifications and filings.
• Verify manufacturing/site info aligns with regulatory dossiers.
• Identify and document CoA discrepancies and impact on release.
• Escalate blocking discrepancies to regulatory and distribution teams.
• Complete endorsement/release forms in quality systems (Veeva/LIMS).
• Maintain records of specification and filing versions for audits.
• Ensure compliance with SOPs and cGMP requirements.
• Support QP certification processes (EU/UK) and country-specific releases.

Conocimientos

GMP knowledge

Batch record review

CoA verification

Regulatory familiarity

Cross-functional collaboration

Educación

Bachelor's degree in life sciences, chemistry, pharmacy, or related field

Herramientas

Veeva

LIMS

Descripción del empleo

Build Our Future Together

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Quality Reviewer / Batch Release Specialist supporting clinical and commercial lot release across our global product portfolio. In this role, you will safeguard product quality and regulatory compliance by verifying batch records and Certificates of Analysis against approved specifications, while collaborating with regulatory leads, global regulatory teams, and distribution compliance.

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Quality Reviewer / Batch Release Specialist supporting clinical and commercial lot release across our global product portfolio. In this role, you will safeguard product quality and regulatory compliance by verifying batch records and Certificates of Analysis against approved specifications, while collaborating with regulatory leads, global regulatory teams, and distribution compliance.
This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & Where

• Location: US
• Work model/flexibility: Remote or on-site in Rensselaer, NY (5 days/week)
• Contract duration: 6 months
  

Discover Your Role

• Review batch status forms and CoAs for drug substance, formulated drug substance (and drug product (labeled and unlabeled) to confirm lot disposition (released/quarantined), manufacturer/site, and shelf life/expiry
• Cross-check release testing panels, acceptance criteria, and release results in the CoA against approved specifications (e.g., P.5.1, S.4.1) and current regulatory filings (IMPD, IND, CTA, BLA, MAA)
• Verify manufacturing/testing site information, container closure, formulation, and dosage form align with the applicable regulatory dossier
• Identify and document discrepancies between CoA data and regulatory filings; assess whether discrepancies prevent lot release/endorsement
• Call out blocking discrepancies to appropriate collaborators (e.g., regulatory representatives, global regulatory leads, distribution compliance) for resolution or filing amendment
• Complete and submit required endorsement/release forms in the relevant quality system (e.g., Veeva, LIMS, or equivalent)
• Maintain accurate records of specification versions, filing versions, and prior review outcomes to support efficient future reviews
• Ensure activities follow applicable SOPs, work instructions, and cGMP requirements
• Support QP certification processes (EU/UK) and country-specific release requirements
  

This Role Requires

• A Bachelor's degree in life sciences, chemistry, pharmacy, or related field (advanced degree a plus) and 2+ years' experience in pharmaceutical/biotech Quality Assurance, Quality Control, Regulatory Affairs, or CMC operations.
• Working knowledge of GMP, batch record review, and lot release/disposition processes
• Familiarity with regulatory filing structures (CTD Module 3, IMPD, IND, BLA/MAA)
• Experience with clinical trial or commercial lot release preferred
• Familiarity with QP certification processes and global distribution compliance preferred
  

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.