Teva Pharmaceuticals Ltd Job Opening for Regulatory Affairs Department |
Teva Pharmaceuticals is hiring for Regulatory Affairs-EU Post Approvals who can fulfill the following criteria.
Job Location: Mumbai-Seawoods
Years of experience: 3-6
-Experience in handling end to end post approval activities in EU Market.
-Experience in handling variation filings,query responds & renewal activities.
-Prepare,compile,review and submit high quality submissions for all required post approval activities in accordance with EU legislation and in-house standards.
-Responsibility for MA compliance with both legislation and business needs.
-Ensure approvals are secured within the stipulated timelines for designated projects.
-Maintain registration documentation and associated electronic databases, inline with house procedures.
-Provide regulatory support and product information for all internal and external customers, stakeholders and TEVA project teams.
-Prioritise, plan and monitor submissions for allocated procedures while documenting and informing involved parties of progress.
If your profile matches the above requirement, please share your updated resume to mounika.alluri@lotuslabs.com with subject line as “Regulatory Affairs-EU Post Approvals”
Regards
Teva Recruitment Team.
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