Responsible to establish and maintain a group of high performing regulatory affairs professionals working in an efficient, productive and harmonized fashion to support the execution of company plans in Hong Kong.

Closely collaborate with regional regulatory expertise in the Therapeutic Areas in both labelling and CMC aspects.

Design, deploy and maintain processes and/ or systems to manage external stakeholders, of which includes local change implementation management. External stakeholders include, but not limited to, provision of documents and liaison with local third party, government tendering bodies, Hospital Authority, etc.

Provide regulatory support, including oversight of product launch and implementation timelines to internal and external stakeholder.

Accou...