location_onSerilingampalle (M), Telangana, India
watch_later Posted: Mar 29, 2025
Job Description
Regulatory Affairs expertise with medicinal products for changes with impact on Product Information - Safety / Labelling changes, including CCDS creation or updates
Experience
Experience
- 4-7 yrs of Regulatory Affairs experience in EU/UK/CH/AU/NZ:
- Safety Labelling changes with impact on Product Information and management of AW updates from an RA perspective
- CCDS creation or updates prior experience preferable
- Change control assessments
- Experience working on Centralized products is a plus
- Veeva RIMS Knowledge.
- Knowledge in using TVT Tool is a plus.
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