北京招聘

Contact us to start your exciting career development in a collaborative, dynamic and stimulating work environment in Fortune 500 multinational pharmaceutical company.

Responsitilities:
1. Ensure the testing timeline was achieved;
2. Ensure the new products application, license renewal and variations registration is managed according to the timeline specified in the reporting period.
3. Bridge clear, adequate and effective communication with global RA to ensure China requirements and processes are well understood;
4. Support business post-market needs, including but not limited to label & IFU review, port testing support and etc;
5. Maintain the close working relationship with CFDA, testing labs and other government agencies;
6. Business & regulation acumen; provide professional solution to support sustainable business growth;
7. Set up and maintain regulatory database in an efficient manner;
8. Set up and maintain an approachable dossier archive system; make sure all dossiers submitted to agency was retained according to company policy;
9. Support team daily operation including but not limited to sample management, contract & payment coordination, set up team & cross function meeting.

Job Requirements：
1. Bachelor degree in pharmacy or related science;
2. Over 1 year working experience in pharmaceutical industry (RAspecialist);
3. Good management of time;
4. Fast learning capability;
5. Good written English.