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.




- Strong 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

Benefits:
- Health insurance
- Leave encashment
- Paid sick time
- Provident Fund

Work Location: In person

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