Full-time

Associate Regulatory Affairs Manager

Posted by Abbott • Beijing, China, China

📍 Beijing, China 🕒 June 06, 2026

About the Role

**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.
+ Conduct ...

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