Specialist, Regulatory Data Stewardship (xevmpd / Idmp)

Vetamc

Hyderabad, , India
Hybrid
Xevmpd submissions management
Idmp data governance
Evweb and veeva vault rim proficiency
Join a global healthcare biopharma company with a 130-year legacy dedicated to innovation and improving global health

Job Summary

  • Join a global healthcare biopharma company with a 130-year legacy dedicated to innovation and improving global health.
  • Play a pivotal role ensuring the quality and regulatory readiness of product registration data impacting patients using life-saving products.
  • Be part of a globally distributed technology center team driving digital transformation and delivering business solutions that save and improve lives.

Matching Summary

Join a global healthcare biopharma company with a 130-year legacy dedicated to innovation and improving global health.

Skills & Requirements

Must-have

  • XEVMPD submissions management
  • IDMP data governance
  • EVWEB and Veeva Vault RIM proficiency
  • Regulatory data quality assurance
  • European Medicines Agency compliance
  • Data migration and enrichment
  • Regulatory reporting and documentation

Nice-to-have

  • Power BI familiarity
  • Cross-functional project collaboration
  • Methodical and adaptable work style
  • Effective communication and collaboration
  • Use of Microsoft 365 apps
  • Digital transformation focus

Key Requirements

  • Bachelor’s degree in scientific or IT discipline
  • Minimum 4 years regulatory affairs or operations experience
  • Strong knowledge of XEVMPD, IDMP, SPOR, and RIM systems
  • Understanding of European regulatory framework including SmPC and Module 3
  • Experience with EVWEB, Veeva Vault RIM, SharePoint, Microsoft 365
  • Experience in cross-functional and matrix organizations

Work Rights

Not specified

Tailored Resume

Cover Letter