Regulatory Affairs @ Shhy India

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Regulatory Affairs

Shhy India
3 - 4 Years
Hyderabad
4 years ago
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Job Description

1. Responsible to collect DMF documents according to NMPA's requirements. Control the timeline of DMF submission from manufacturer, if any delay, find out the real reason and find an efficient solution.
2. Responsible to coordinate RA department and provide support to RA colleagues of China HQ. Planning to visit manufacturers corporate office or plant to meet their RA people, win their trust.
3. Report to RA manager for other assigned tasks.
4. Keep track of orders, shipments, and quality through coordination with the suppliers. If necessary, on-site inspection will be needed.
5. Responsible to handle daily affairs in India office.

Employement Category:

Employement Type: Full time
Industry: Pharmaceutical
Functional Area: Pharmaceutical
Role Category: Regulatory Affairs Executive
Role/Responsibilies: Regulatory Affairs

Contact Details:

Company: Shhy India
Location(s): Hyderabad

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Functional area / Department (*):

Enter Skills (key skills, subjects, technologies & roles to use in search)

Write briefly about yourself, your experience and education (*)

Attach ResumeMax 2.38 MB (RTF, PDF, DOC, DOCX formats only parsed)

Please, check the file size and type.

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Shhy India

CHINA CHINOPHARMA LTD (CSC) was established in 2002, we are an agency company who specializes in dealing with pharmaceutical products, based on the Chinese market. CSC is one of 123 local companies in Shanghai who was granted with GSP certificate, and became one of 2 local companies in Shanghai who ...

Regulatory Affairs @ Shhy India

Home > Regulatory Affairs Executive