Manager, Regulatory Affairs

Found in: beBee S CN - 1 month ago

Beijing, China MSD Full time

Job Description

Position Overview

Manage registered products and lead projects to register new products within the team agreed timeline.

l Communicate with international RA team contactor

l Preparing registration dossiers and relative question

l Follow up registration procedure

l Make good relationship with officials

l Supervise registration officer to prepare dossiers

l Organize the registration evaluation meeting

l Coordinate Q.C. re-confirmation test with institute for drug control

l Get final registration permits

l Get related registration regulations with update

l Provide RA input on the strategic planning for all responsible products

Requirements

l At least 6 years working experience in pharma. Industry

l Over 5 years’ experience in registration field

l Bachelor and above in medicine , pharmacy or related disciplines

l Good computer skill in EXCEL, POWERPOINT and WORD

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):


Requisition ID:R284955

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