职位描述：
职责描述：
1. be responsible for documents preparation and review for drug registration and make sure the progress from filing to approval.
2. follow up and study local/international regulations
3. collaborate with relevant departments and involve in regulatory strategy and policy development
4. be responsible for providing regulatory supports to other departments
任职要求：
1. bachelor degree or above with major in medical / bioengineering / biochemistry or other related subjects;
2. at least 2 years in regulatory affairs and familiar with drug registration process, regulation and standards;
3. common communication skill in english;
4. good experience in biological product registration is preferred;
5. working experience in foreign company is preferred;
6. proficient in the use of ms office