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Associate Regulatory Affairs Manager

📍 Abbott • Beijing, Beijing, China • Posted June 21, 2026

Full-time Posted June 21, 2026
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Job Description

Primary Function/Primary Goals/Objectives: 

  • Secure existing drug products registration submission and approval on time to protect the business continuity.
  • Ensure drug post-market regulatory compliance including formulation, label, leaflet, ingredient, change control, promotional materials, etc.
  • Provide regulatory support to innovations/new projects, and regulatory training to internal stakeholders.
  • External engagement with regulators, and industry association on new legislations monitoring regulation changes, and policy influence. Manage the internal legislation database.

    • Major Responsibilities:

  • Manage the planning, preparation, and submission of drug product registration dossiers, ensuring they meet all relevant regulatory requirements and deadlines.
  • Lead the development of robust regulatory strategies, integrating business goals and gaining consensus across local and divisional teams from various functions.

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