JAMP Pharma’s hiring for Regulatory Affairs is focused on finding professionals skilled in navigating the complex regulatory landscape of the pharmaceutical industry.
REGULATORY AFFAIRS – eCTD
Officer / Senior Officer / Executive
Key Responsibilities:
• eCD Compilation, validation, and submission to Health Canada and US through ESG gateway for : New Submission (ANDS/NDS), Deficiencies response (Clarifax, SDN, NOD, NON etc.), Supplements submissions (SANDS, ARs, Safety updates, RMPs etc.).
• eCTD Compilation, validation, and submission to export market.
• eCTD lifecycle management of products.
• Maintaining daily submission tracking.
• Implementing & Maintaining Document Management System.
Specifications:
• Department: Regulatory Affairs – eCTD
• Experience: 1 – 5 years
• Qualification: B. Pharma / M. Pharma / M.Sc
• Location: Ahmedabad
Send profile at
[email protected]
