Job responsibilities:

1, have more than one year relevant working experience

2, participate in the complete international registration documents preparation and follow-up tracking work

3, responsible for the international registration file file work

4, participate in the complete product process changes

5, responsible for foreign clients survey work

6, participate in foreign official/customer audit technology and regulations documents preparation and after the rectification work

7, collection of GMP and registration related laws and regulations of the file, and file

8, tracking, laws and regulations related to the completion of the CAPA

9, responsible for registration related foreign data translation

10 and assist other departments work, and to undertake other work assigned by the leadership of the company

Job requirements:

1, pharmacy, chemistry, microbiology or bachelor degree or above, major in pharmacy or related

2, have certain medicine, pharmacology, pharmaceutical, biochemical, pharmaceutical multiple domain knowledge reserves

3, understand the domestic and international registration registration regulations, technical requirement and working process

4, have good professional dedication and team spirit

5, have good communication and public relations capacity

6, have strong ability to read and write in English, can draw up the general technology and regulatory documents in both Chinese and English, good command of computer operation

4, good