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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Manager CMC Regulatory Affairs - Combination Products

Regulatory & Quality (Life Sciences)Updated on Nov 5
Full-timeRensselaer, NY, USA$108k - $176k /yr

About the Job

Requirements

  • A bachelor’s degree with at least 6 years of related experience, or an advanced degree with at least 3 years of related experience in pharmaceutical or biotechnology settings.
  • 2–4 years of CMC Regulatory Affairs experience supporting worldwide regulations.
  • Strong understanding of global CMC Regulatory Affairs requirements, including combination products and human factors.
  • Experience delivering marketing authorizations, CTA/INDs, and post-approval submissions.
  • Ability to assess regulatory impact, support compliance activities, and mentor junior staff.
  • Ability to support training activities and proactively address technical or regulatory knowledge gaps.
  • Strong communication, negotiation, strategic thinking, problem-solving, prioritization, and cross-functional collaboration skills.

Responsibilities

  • Support combination product development from early phase through post-market activities.
  • Review regulatory filings, including INDs, BLAs, MAAs, annual reports, and supplements.
  • Develop design control documentation and quality systems for combination products.
  • Assess changes and deviations for regulatory impact and submission requirements.
  • Support regulatory authority meetings, responses, and inspections.
  • Create standard operating procedures, Working Instructions, and Reviewer’s Guides.
  • Identify process gaps and support regulatory intelligence activities.
  • Translate ambiguity into action and build effective stakeholder partnerships.

Desired Qualifications

  • Experience supporting biologics and combination products.
  • Experience engaging with the FDA or other regulatory authorities.

About the Company

Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Regeneron Pharmaceuticals develops and commercializes medicines for serious diseases, with a focus on cancer, eye diseases, allergic and inflammatory diseases, and infectious diseases. Its products come from using proprietary research capabilities and technologies to discover and develop therapies, often in collaboration with academic, research, and industry partners. Revenue comes from selling approved medicines and from licensing its technologies and entering co-development and co-commercialization partnerships. The company works with healthcare providers and regulators to ensure treatment delivery and safety. Its goal is to improve patient outcomes by bringing life-transforming medicines to market through rigorous R&D and strategic collaborations, maintaining leadership in biopharmaceutical innovation.

Company size
10,001+
Company stage
IPO
Headquarters
Town of Mount Pleasant, New York
Founded
1988

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