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BeOne

Global oncology therapeutics discovery, development, manufacturing

Senior Director - Regulatory Affairs, CMC

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeRemote in USA$204.5k - $274.5k /yrRemote

About the Job

Requirements

  • A BA/BS degree in a scientific discipline is required.
  • At least 12 years of relevant industry experience is required.
  • A demonstrated track record of leading ADC programs from IND through BLA/MAA and Health Authority interactions is required.
  • Strong people leadership and the ability to develop and lead a high-performing team are required.
  • Ability to work effectively in a global, culturally diverse, and matrixed project team is required.

Responsibilities

  • Lead and develop a U.S.-based Regulatory CMC team overseeing CMC regulatory strategy and execution for the ADC portfolio across all phases of development and lifecycle management, including CMC dossier authoring, Health Authority interactions, and ensuring technical excellence and regulatory compliance.
  • Serve as Global Regulatory Lead for a late-stage ADC program advancing toward BLA submission; lead regional members and own the program’s global CMC regulatory strategy, execution, Health Authority interactions, regulatory risk assessment and mitigation, CMC dossier preparation and finalization, and lifecycle management in accordance with applicable regulations and guidelines.
  • Partner with global cross-functional stakeholders, including CMC, Manufacturing, Quality, Supply Chain, Clinical, and GRA teams, to align on ADC CMC regulatory strategies, development plans, and execution.
  • Lead and oversee regulatory CMC change-control impact assessments for ADC programs, ensuring appropriate regulatory strategies and filings are identified and executed in a timely and compliant manner.
  • Lead and oversee regulatory risk management across the ADC portfolio by identifying CMC-related regulatory risks, defining mitigation strategies, and escalating critical issues to senior management as appropriate.
  • Establish, maintain, and continuously improve Regulatory CMC standard operating procedures, working instructions, and best practices to ensure consistency, compliance, and inspection readiness.
  • Ensure appropriate Regulatory CMC assessment, strategy, and execution in support of ADC product quality issues, including recalls, deviations, and product complaints throughout the product lifecycle.
  • Review and approve Regulatory CMC documentation, including submissions, responses, and internal procedures, within the Regulatory Information Management system.
  • Lead or oversee Regulatory CMC due-diligence activities for business development, licensing, and acquisition opportunities, including risk and gap assessments.
  • Represent the company and Regulatory CMC function in external forums, industry groups, and regulatory or scientific conferences as appropriate.
  • Manage a team of about five people based in the United States and manage a global project team in a matrix model.

Desired Qualifications

  • An MS or PhD is preferred.

About the Company

BeOne

Global oncology therapeutics discovery, development, manufacturing

BeOne Medicines discovers, develops, and commercializes oncology therapies worldwide, focusing on hematologic cancers and solid tumors. Its products work by leveraging internal R&D and clinical development to bring therapies to market quickly, with Brukinsa serving as a leading backbone in the US and European markets. It differentiates itself through a large-scale global clinical network and cost-efficient development and manufacturing that support high margins and a focus on large-market cancer indications. Its goal is to expand access to high-impact, affordable cancer treatments across more than 45 countries while growing its pipeline into immunology and solid tumors.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Dongcheng District, China
Founded
2010

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