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Assistant Manager Regulatory Affairs
Umedica Laboratories Private Limited
Mumbai | Navi Mumbai / Panvel
Not Disclosed
10 - 15 Years
Full Time - Permanent
Views:3
Applicants:0
Posted on 1 Jun, 2026
In Office
Job Description | Responsibilities
- Plan, prepare, review, and submit regulatory dossiers for TGA and Health Canada, including new product registrations (ARTG entries, NDS), variations, renewals, and post-approval supplements in eCTD format.
- Contribute to departmental goal setting, planning, and reporting activities under the supervision of AGM–Regulatory Affairs.
Overview
- Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
- Functional Area - Research / R&D - Pharma / Medical / Health / Biological Sciences
- Job Role - Research Scientist - Pharma API
- Employment type - Full Time - Permanent
- Work Mode - In Office
Qualifications
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
Regulatory Affairs (RA)
API Regulatory Submissions
Dossier Preparation
Regulatory Documentation
Regulatory Compliance
Regulatory Strategy
Assistant Manager Regulatory Affairs
