Specialist, Regulatory Data Stewardship (xevmpd / Idmp)

Muckelab

Hyderabad, India
Hybrid
Xevmpd submissions management
Idmp data governance
Evweb and veeva vault rim proficiency
Be part of a global healthcare biopharma company with a 130-year legacy focused on innovation and ethical integrity

Job Summary

  • Be part of a global healthcare biopharma company with a 130-year legacy focused on innovation and ethical integrity.
  • The Regulatory Data Steward ensures the quality and regulatory readiness of product registration data impacting life-saving products.
  • Join a team passionate about using data, analytics, and insights to drive decision-making and support global healthcare advancements.

Matching Summary

Be part of a global healthcare biopharma company with a 130-year legacy focused on innovation and ethical integrity.

Skills & Requirements

Must-have

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

Nice-to-have

  • Power BI familiarity
  • Cross-functional project teamwork
  • Effective communication and collaboration
  • Methodical and adaptable work style
  • Data migration and enrichment experience

Key Requirements

  • Bachelor’s degree in scientific or IT discipline
  • Minimum 4 years regulatory affairs or operations experience
  • Strong knowledge of XEVMPD/EVPRM, ISO IDMP, SPOR, RIM systems
  • Understanding of European regulatory framework and SmPC/Module 3
  • Experience with data migration and enrichment projects

Work Rights

Not specified

Tailored Resume

Cover Letter