Job Information
J&J Family of Companies Regulatory Affairs Specialist in Shanghai, China
Regulatory Affairs Specialist - 2407022216W
Description
What You Will Do
The Regulatory Affairs Specialist is responsible for：
Responsible for registration operation level on drug registration (register/renewal/variation/outside testing etc.);
Regulatory related consultation and other regulatory support to business on OTC. Ensure full regulatory compliance for whole life cycle product management.
Proactive to build and maintain good relationship with stakeholders.
Responsible for department PR/PO/payment/invoice, supplier management in Aravo.
Support on team Accrual and department daily management work.Proactive to support line manager and / or need state
Qualifications
What We Are Looking For
Required Qualifications
Bachelor’s /master degree
At least 2 years working experience of pharmaceutical industry. With experience of regulatory affair, manufacturing or quality assurance is preferred.
Project budget management and vendor communication exprecience is preferred.
English and Mandarin speaking at least intermediate.
Proactive to learn and solving problem.
Communication skill
Preferred base in Shanghai
Primary Location Asia Pacific-China-Shanghai-Shanghai
Job Function Regulatory Affairs
Req ID: 2407022216W
J&J Family of Companies
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