The role involves supporting regulatory affairs activities, maintaining regulatory documentation, and ensuring compliance with applicable industry guidelines and company procedures. The candidate will coordinate documentation, track regulatory submissions, and work with internal teams to ensure timely completion of regulatory requirements.

Qualification:

• Prepare and maintain regulatory documents, records, and submission trackers.
• Support regulatory submissions, renewals, amendments, and approval documentation.
• Ensure regulatory records are accurate, organized, and updated.
• Coordinate with internal teams to collect required documents and information.
• Monitor regulatory updates and support compliance with applicable guidelines.
• Maintain documentation required for audits and inspections.




• Track submission timelines and follow up on pending approvals.
• Support regulatory activities related to pharmaceutical products, medical devices, or clinical research, as applicable.
• Bachelor's or Master's degree in Pharmacy, Biotechnology, Life Sciences, or a related field.
• Relevant experience in Regulatory Affairs within the pharmaceutical, healthcare, or clinical research industry.
• Knowledge of regulatory documentation and compliance requirements.
• Valuable communication, coordination, and documentation skills.
• Working knowledge of MS Office, particularly Excel and Word.

📌 Executive, Regulatory Affairs (New Delhi)
🏢 Intrinseque Health
📍 New Delhi