LYRUS is a forward-thinking pharmaceutical company committed to innovation and excellence in drug development and regulatory compliance. With a focus on delivering high-quality pharmaceutical products globally, LYRUS operates with the motto ThinkDesign Deliver, ensuring every project meets stringent regulatory standards across multiple regions including the EU, GCC, South Asia (SA), and Rest of the World (ROW).
Job Description
As a Senior Officer / Executive Regulatory Affairs, you will be responsible for:
- Preparing and managing regulatory dossiers (Modules 1-3) for pharmaceutical products.
- Ensuring compliance with regulatory requirements across various regions such as EU, GCC, SA, and ROW.
- Coordinating with cross-functional teams to gather necessary documentation and data for dossier submission.
- Monitoring regulatory changes and updating dossiers accordingly.
- Liaising with regulatory authorities to facilitate approvals and registrations.
- Supporting the regulatory strategy and ensuring timely submissions.
Eligibility Criteria
- Educational Qualification: B.Pharm / M.Pharm
- Experience: 3-4 years in Regulatory Affairs (RA)
- Expertise in dossier preparation, specifically Modules 1-3.
- Experience working with regulatory frameworks in EU, GCC, SA, and ROW regions.
Application Link
