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Posted on 31 Aug, 2026
In Office
Job Description | Responsibilities
- Prepare and maintain regulatory submissions and documents.
- Support product registrations, renewals, and variations.
- Review regulations and ensure compliance.
- Coordinate with QA, R&D, and cross-functional teams.
- Track submissions, approvals, and regulatory records.
Overview
- Industry - Medical Devices / Equipments
- Job Role - Regulatory Affairs Associate
- 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
Regulatory Submissions
Compliance
Product Registration
CTD/eCTD
Lifecycle Management
Documentation
QA
Medical Devices