Work address:

Shenyang, Beijing, Shijiazhuang,New York

Responsibilities:

1. Review, draft or prepare drug registration documents to ensure the quality of application materials;
2. Be responsible for the submission of registration documents, track the progress of the review, deal with all kinds of common problems encountered in the registration inspection and issuance of supplementary replies at any time;
3. Provide consultation on regulations related to drug registration for customers and company projects.
4. As a mentor, provide technical guidance and training to RA Managers and specialists.
5. Perform other tasks assigned by the supervisor.

Qualifications:

1. Master degree or above in pharmaceutical analysis, pharmacy related majors, minimum 3-5 years of drug registration work experience;
2. Excellent oral/written communication skills inEnglish;
3. Responsible for or leading atleast5 drug registration projects, with strong independent thinking and judgement;
4. Determined to work in drug registration.Drug research and development experience is preferred;
5. Lively and cheerful personality withcertain ability to resist pressure.

Send your resume to: xizimed@xizimed.com