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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Manager CMC Regulatory Affairs

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeTokyo, JapanNo salary listed

About the Job

Requirements

  • A bachelor's degree in a scientific discipline is required; a master's degree is preferred.
  • Strong biopharmaceutical and regulatory Chemistry, Manufacturing and Controls (CMC) background.
  • 15+ years of regulatory CMC experience, including health authority interactions, major submissions, and approvals in Japan.
  • Experience leading CTN, J-NDA, eCTD submissions, PCA, MCN, and PMDA responses.
  • Deep knowledge of Japanese regulatory requirements, guidance documents, and regulatory resources.
  • Experience managing submission timelines and delivering filings on schedule.
  • Ability to obtain and maintain Foreign Manufacturing Accreditation or Foreign Manufacture Registration.
  • High fluency in Japanese and English.
  • Ability to interpret regulations and think strategically.

Responsibilities

  • Lead planning, scientific writing, and critical review of CTN, J-NDA, and eCTD supplement submissions.
  • Prepare Japanese application forms and support high-quality regulatory dossiers.
  • Drive regulatory decisions based on requirements while working across cross-functional teams.
  • Act as a local liaison with PMDA for CMC submissions and information requests.
  • Assess CMC change controls against regulatory filings to maintain compliance.
  • Review manufacturing processes and specifications against approved filings.
  • Participate in agency meetings and communicate regulatory positions and feedback.
  • Manage submission timelines and deliver filings on schedule.

Desired Qualifications

  • A master's degree in a scientific discipline.

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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