Posted:8 hours ago|
Platform:
On-site
Full Time
Job Description:
Regulatory Affairs – Dossier Preparation & Lifecycle Management
Requirement- Compulsory 1 year Experience in RA
Key Responsibilities:
Dossier Preparation & Review:
Prepare, compile, and critically review regulatory dossiers (CTD/eCTD format) for submission in compliance with country-specific regulatory guidelines.
Ensure completeness, accuracy, and quality of all submission documents.
Query Management:
Handle and respond to regulatory queries in a timely and efficient manner.
Coordinate with cross-functional teams to gather required clarifications and documentation.
Lifecycle & Project Management:
Manage the end-to-end lifecycle of product registrations including new submissions, renewals, and variations.
Track project timelines, regulatory milestones, and ensure on-time delivery of submissions.
Regulatory Intelligence & Guideline Updates:
Regularly monitor and interpret updates in country-specific regulatory guidelines.
Ensure internal processes and documentation are aligned with the latest regulatory expectations.
Cross-Functional & External Coordination:
Liaise with third-party manufacturers to gather technical documents and compliance-related data.
Collaborate with internal departments such as QA, QC, R&D, and Supply Chain for seamless documentation and query resolution.
Countries of Regulatory Responsibility:
Job Type: Full-time
Pay: ₹15,000.00 - ₹30,000.00 per month
Benefits:
Work Location: In person
Alvita Pharma Pvt.Ltd.
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