Regulatory Affairs Associate I

Employer - Teva Pharmaceuticals
Job title - Regulatory Affairs Associate I

Job Description

Compiling of the Annual Report and ensuring it is submitted prior to the commitment date (at minimum no later than the due date).
Compilation and submission of post approval supplements (CBE 0, CBE 30, PAS) in US.
Coordinating the retrieval of supporting documentation in accordance with the Annual Report schedule.
Retaining all supporting documentation as required in completing an Annual Report.
Notifying Regulatory Affairs Manager or designee (and Quality, if required) that an Annual Report is at risk of being submitted late. Qualifications
3-4 yrs exp M Pharm / MSc or B Pharm Function Regulatory Affairs Sub Function Medical Regulatory Affairs Reports To In process of validation Already Working @TEVA?
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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Job Location Navi Mumbai, Maharashtra
Date Posted 30 Jul 2020
Employer Email --No Email
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