Want to think for yourself? As Regulatory Affairs Associate you’ll have the freedom to forge a career as an expert in a niche, in-demand, business-critical role.

**Regulatory Affairs Associate**
**Hong Kong, Hong Kong**

**Accountability**:
- Provide support to the regulatory activities for all products within Hong Kong
- Compilation of national dossiers for submissions to authorities
- Support the preparation, maintenance and update of product registration/license and regulatory compliance files.
- Developing and maintaining a database of local regulatory requirements.
- Manage assigned product portfolio
- Work with Head of Regulatory and Medical Affairs to execute activities in Hong Kong
- Support local artwork creation and proof-reading
- Support local advertisement and promotional activities to ensure compliance to local regulations
- Support responses on product queries to internal and external customers
- Provide supporting documents for Macau importation and cross-border business

**Requirements**:

- University graduate in biological science / pharmacology
- Minimum 1-2 years’ experience in regulatory affairs, with FMCG, pharmaceutical, medical device experience has advantage
- Results oriented, entrepreneurial and self-motivating
- Good analytical and organizing skills
- Detail oriented and able to work independently
- Work under pressure and tight timeline
- A team player with good communication and interpersonal skills
- Good command of written and spoken English and Chinese

**Equality**:
All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.