IN EmploymentAlert | ProPharma | Regulatory Affairs Specialist
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Job Title


ProPharma | Regulatory Affairs Specialist


Company : ProPharma


Location : Vijayawada, Andhra Pradesh


Created : 2025-01-07


Job Type : Full Time


Job Description

We are seeking a highly skilled Regulatory Affairs Associate or Junior Regulatory Affairs Manager with proven expertise in Veeva Vault to join our team on a 6-month contractual basis with the potential for extension. The ideal candidate will support regulatory data reconciliation and content management efforts, ensuring accurate and streamlined operations within Veeva Vault.Key ResponsibilitiesData Reconciliation and Clean-Up:Perform thorough reconciliation and clean-up of regulatory data within Veeva Vault.Ensure data accuracy, consistency, and completeness.Collaboration with Regulatory Teams:Work closely with regulatory product teams to streamline processes and achieve reconciliation goals.Act as a liaison between teams to address system and data-related challenges.Data Monitoring and Reporting:Generate and analyze reports to track data quality and monitor project progress.Identify and resolve issues related to data discrepancies.Global Submission Content Plans:Build and manage Global Submission Content Plans within Veeva Vault on behalf of regulatory product teams.Issue Resolution:Investigate and resolve discrepancies or errors in regulatory data systems.Ensure smooth operation of Veeva Vault functionalities and workflows.Experience:Proven expertise in working with Veeva Vault.3+ years of experience in Regulatory Affairs or related fields (preferably in the pharmaceutical or life sciences industry).