We’re Hiring: Regulatory Affairs Executive
Location: Nehru Place, New Delhi | Company: Medical devices. | Employment Type: Full-time

Are you experienced in drug regulations, licensing, and compliance?
Do you have hands-on knowledge of CDSCO, FSSAI & MDR ? Then this opportunity is for you.

About the Role:
We are looking for a detail-oriented Regulatory Affairs Executive who can manage regulatory compliance, product registrations, and licensing processes across medical devices.

Key Responsibilities:
Handle medical device registrations
Prepare and submit regulatory documents as per CDSCO guidelines
Manage drug licenses, import/export licenses, and approvals
Ensure compliance with CDSCO, FSSAI, and other regulatory authorities
Stay updated with changing regulatory laws and policies

Requirements:
Experience in Regulatory Affairs & MDR Compliance.




Robust knowledge of CDSCO regulations and licensing procedures
Hands-on experience in document preparation and submission
Understanding of drug & medical device approvals
Valuable communication and documentation skills

Preferred Profile:
Experience in handling import/export compliance (IEC, AD Code, etc.)
Familiarity with FSSAI, GST, BIS, or other compliance frameworks
Detail-oriented with strong follow-up skills

Why Join Us?
Work with a fast-growing Medical Device firm.
Exposure to diverse regulatory projects
Supportive and growth-focused work environment

Pay: ₹35,000.00 - ₹40,000.00 per month

Advantages:
Health insurance
Leave encashment
Paid sick time
Provident Fund

Work Location: In person

📌 Regulatory Affairs Executive Delhi
🏢 MED-EL India
📍 Delhi