Specialist, Regulatory Data Stewardship (xevmpd / Idmp)
Merck & Co., Inc., Rahway, New Jersey, USA
Hyderabad, India
Hybrid
Xevmpd reporting
Idmp-related data activities
Evweb and veeva vault rim
Be part of an organisation driven by digital technology and data-backed approaches that support a diversified portfolio of prescription medicines, vaccines, and animal health products
Job Summary
Be part of an organisation driven by digital technology and data-backed approaches that support a diversified portfolio of prescription medicines, vaccines, and animal health products.
As a Regulatory Data Stewards, you will play a pivotal role ensuring the quality of our regulatory data within regulatory domains, which will directly influence patients who use our life-saving products.
Our Technology Centers focus on creating a space where teams can come together to deliver business solutions that save and improve lives.
Matching Summary
Be part of an organisation driven by digital technology and data-backed approaches that support a diversified portfolio of prescription medicines, vaccines, and animal health products.
Skills & Requirements
Must-have
XEVMPD reporting
IDMP-related data activities
EVWEB and Veeva Vault RIM
regulatory data quality
European regulatory framework
Nice-to-have
data-backed approaches
digital transformation journey
passion for using data
intellectually curious
empathy, creativity, digital mastery
Key Requirements
Bachelor’s degree in scientific or IT discipline
Minimum 4 years' experience
Industry regulatory standards and initiatives
Summary of Product Characteristics (SmPC) and Module 3 knowledge
Experience in data migration and enrichment projects