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BeOne

Global oncology therapeutics discovery, development, manufacturing

Director of Regulatory Affairs

Regulatory & Quality (Life Sciences)Updated on Nov 6
Full-timeRemote in UK£96.9k - £121.1k

About the Job

Requirements

  • A bachelor's degree is required.
  • At least 10 years of experience in the biotechnical or pharmaceutical industry and at least 15 years of experience in a Regulatory capacity with a broad background are required.
  • Experience working with MHRA regulatory procedures is mandatory.
  • A sound understanding of the drug development process, the pharmaceutical industry, the healthcare environment, UK regulatory requirements, and policy trends is required.
  • Extensive experience with Microsoft Office, Veeva regulatory publishing, and PowerPoint presentation authoring and presentation is required.

Responsibilities

  • Develop and implement UK regulatory strategies for development programs to secure and maintain product marketing authorization in line with business objectives and in coordination with internal stakeholders.
  • Lead the UK Regulatory Affairs team in managing regulatory aspects of designated compounds, including new molecular entities and new indications, through development, registration, post-approval, and product lifecycle stages.
  • Collaborate with internal stakeholders to develop, implement, and maintain regulatory strategies for new product submissions, including marketing authorization applications, and oversee regulatory aspects of early-stage development programs in line with global product development objectives and UK business goals.
  • Manage the content of and prepare UK marketing authorization application dossiers; understand EU marketing authorization application dossiers to support labeling updates and management in Ireland in compliance with UK and Ireland regulatory requirements.
  • Oversee and be accountable for regulatory agency communications, submissions, and approvals, with a quality focus on securing first-cycle approvals.
  • Support product launch activities.
  • Review and provide input into promotional materials for the UK and Ireland.
  • Act as the Regulatory Affairs liaison within the UK Leadership team, attend regular meetings, and provide input into UK business strategy.
  • Prepare the team for Health Authority interactions, moderate and lead discussions, serve as the main MHRA contact for strategic non-study-specific topics, and support the EU Regulatory Affairs team on clinical Health Authority matters.
  • Anticipate and mitigate regulatory risks while maintaining current knowledge of regulatory intelligence, procedures, changes, and trends.
  • Provide submission gap analyses, identify potential risks, and propose solutions and mitigation plans to ensure successful submission acceptance.
  • Ensure compliance with global, EU, and UK regulatory requirements.
  • Lead and mentor junior team members.
  • Represent BeOne at UK industry association meetings and congresses.

Desired Qualifications

  • An advanced degree is preferred.
  • Recent experience with oncology products and marketing authorization applications, orphan drug designation, and pediatric investigation plans 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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