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13.0 - 15.0 years
0 Lacs
hyderabad, telangana, india
On-site
Summary The primary objective of this position is to serve as a consultant and advisor, offering expert guidance to enhance complex global business processes, products, and services in Regulatory Affairs. We seek a seasoned professional in GDD Regulatory Affairs who will lead both the strategic and operational implementation of Veeva Vault capabilities for Regulatory Registration Module. This role is responsible for ensuring alignment with organizational objectives, regulatory requirements, and enterprise architecture standards, whilst promoting product innovation and managing the lifecycle. As Associate Director Service Delivery, you will be responsible for leading and coordinating all phas...
Posted 1 day ago
1.0 - 3.0 years
2 - 5 Lacs
navi mumbai
Hybrid
Role & responsibilities Manage Tevas data in accordance with requirements for xEVPMD in order to maintain Tevas Article 57 compliance Provide a Central Data Service for the creation and maintenance of GRA product registration data in line with the global needs of Teva Global Regulatory Affairs. Provide SME services for data management in current and future regulatory data systems Preferred candidate profile Required: Bachelors or Master’s degree in Life Sciences or Information Technology. Preferred: MS in scientific or information technology discipline. Required: 1-3 years (Preferred experience in regulatory operations/affairs) for RMS in EU market
Posted 6 days ago
2.0 - 6.0 years
0 Lacs
maharashtra
On-site
You will be responsible for handling regulatory affairs in XEVMPD (Extended Eudravigilance Medicinal Products Dictionary) and RIMS. The ideal candidate should have a minimum of 2-5 years of relevant experience in this field. Additionally, experience in veeva-vault for creating RO/SO events, XEVMPD submission, and knowledge of IDMP and QMS database will be beneficial for this role. The position is based in Mumbai.,
Posted 2 months ago
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