Job Descriptions

• To provide executive support in product registration and/or premarket procedures for Hong Kong and overseas markets, including but not limited to preparation and submission of registration dossier and maintenance of registration database in a timely manner
• To assist in handling communications with regulatory bodies in Hong Kong and overseas market
• To assist in pre-launch compliance review of marketing materials text specification and artwork, including but not limited to product labels, inserts and promotional materials
• To renew licenses and maintain license registry for Hong Kong
• To manage department documentation
• To assist in any ad hoc tasks as assigned by Supervisor

Job Requirements

• Higher Diploma or above, preferably in Chinese Medicine, Pharmacy in Chinese Medicine, Pharmacy, Biological Science or other Medical related field
• Experience in regulatory affairs or pharmaceutical industry is preferred but not essential
• Excellent communication & interpersonal skills
• Able to work independently under pressure with attention to details, well-organized and responsible
• Excellent proficiency in spoken and written English and Chinese

Candidates with more relevant experience would be considered as Assistant Regulatory Affairs Manager.

Working Location: Hong Kong Science Park, Tai Po, N.T.

We offer 5-day working week and an attractive remuneration package. Interest parties please click “APPLY NOW”. For company details, please visit www.purapharm.com. 

Our company is an equal opportunity employer. All personal data collected will be used for recruitment purpose only, while the personal data of the unsuccessful applicants will be destroyed within 6 months after the recruitment process.