Job Description
Compiling of annual report and ensuring it is submitted prior to the commitment date 9at 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.
Post Name: Regulatory Affairs Associate I
Qualification: M.Sc/M.Pharm/B.Pharm
Experience: 3-4 years
Location : Navi Mumbai IN
Vacancies: NA
Salary : NA
Contact Details :
Company: Teva Pharmaceuticals
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Teva Pharmaceuticals-Hiring M.Sc/ M.Pharm/ B.Pharm for Regulatory Affairs Associate I
