Job Description
Your Journey Starts with Delmege
Senior Executive – Regulatory Affairs – Device
Key Responsibilities
- Handle end-to-end medical device registration with NMRA
- Prepare, review, and submit device dossiers in compliance with NMRA guidelines
- Coordinate and follow up with NMRA officials on submissions, queries, and approvals
- Liaise with principals/manufacturers for required documentation
- Maintain regulatory documentation and ensure timely renewals and variations
- Strong communication and coordination skills
- Attention to detail and regulatory compliance focus
- Ability to work under pressure and meet deadlines
- Flexibility and willingness to work extra hours when required
Qualifications & Experiences
- Pharmacist or Non-Pharmacist candidates are encouraged to apply
- Proven experience in medical device registration
- Strong knowledge of NMRA regulatory requirements and submission processes of DEVICE Dossiers
- Hands-on experience in NMRA follow-ups, dossier preparation, and regulatory coordination
- Ability to manage multiple product registrations and timelines efficiently
