Job opportunity with Teva Pharmaceuticals
Job title: PV Associate III
Job location: Bangalore(work from office)
Years of work experience: 8+ years in PV
Job responsibilities:
- Preparation of periodic safety reports, PADERs, for the USA regulatory agency (FDA).
- Medical review of PADERs.
- Quality control of PADERs.
- Administrator, Quality Approver, Submitter, Writer, MD, QC role in the TrackWise system.
- Maintenance of the TrackWise system.
- Literature review for NDA Annual Reports submitted to the FDA.
- Preparation of Standard Operating Procedure (SOP) documents, Working Instructions (WI), and Manuals.
- Inspection/audit interviewee.
- Other tasks assigned by the direct manager.
Kindly apply on the below job link if its matching your skillsets:
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