Requirements : B. Pharm/M. Pharm & 3-5 years of work experience in similar role.
Core Competencies
- Develop and implement regulatory strategies for product registration in emerging markets specifically SEA, Middle east, Africa & Latin America.
- Identify country-specific regulatory pathways, requirements, and timelines
- Artworks, Change request, FGEX creation & BOM Initiation
- Good Communication, and presentation Skills
- Digital /Excel / Power point / word proficiency
- Compile, review, and submit dossiers for product registrations. eCTD dossier experience preferable.
- The role ensures that pharmaceutical products comply with country-specific regulatory requirements throughout their lifecycle, from dossier submission to post-approval maintenance
- Manage submissions such as: Response to queries, Variation/Post approval changes, Retention & Renewal.
- Maintain product licenses, artwork and regulatory databases
- Provide visibility of upcoming approvals for effective Current Product launch activities.
- Should be well verse with Artwork software for Initiation of artwork and follow-up to ensure that Artworks approval for AH products.
- Initiate, follow-up and approval of all CRFs
- Master Data Management Creation FGEX, Sale test & BOM
- Cross Functional Collaboration for specific issues resolution.
📌 Executive_ Regulatory Affairs_ International Animal Health (Ahmedabad)
🏢 Intas
📍 Ahmedabad
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