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

Similar Jobs