At Freyr Solutions, I manage regulatory documents and submission records in Veeva Vault RIM, including importing eCTD sequences as submission archives.
I track registration data with business stakeholders, investigate system and migration issues, and support data corrections and verification. I also monitor reports and system updates and perform remediation and data enrichment aligned with Veeva releases.
For newly acquired partner molecules, I manage archival and submission activities and check migrated dossiers for document usability and readiness. I also support onboarding and mentoring of new team members.
Previously, at Parexel International Pvt Ltd, I managed regulatory information and product lifecycle data for medicinal products, vaccines, and medical devices. I worked on data reconciliation and quality reviews, market authorization applications, and regulatory requirements including xEVMPD and IDMP.
