1. Documents preparation for regulatory application;
2. Registration and archiving documents;
3. Contribution to all operations related to regulatory affairs, eg. auditing, sampling…
4. Any other work assigned by quality manager.
5. Assist lab tests when necessary after training.
REQUIREMENTS
－Bachelor qualification or above;
－Pharmaceutical and /or biological background, regulatory know is prefer;
－Computer skill: word, excel at least;
－English: Read and write is required, simple communication is advantage.
