Job Description
Avenirr Pharma (Private) Limited
We are looking for a detail-oriented Pharmacist to join our Regulatory Affairs team. This role involves supporting regulatory submissions, document management, compliance tracking and coordination with cross functional teams to ensure timely and accurate regulatory documentation.
Key responsibilities
- Compile and maintain product registration dossiers in line with NMRA and international guidelines (CTD format).
- Coordinate with suppliers, manufacturers, and internal departments to collect and verify regulatory documents.
- Prepare product variation, renewal, and import license applications.
- Maintain tracking systems for regulatory submissions and approvals.
- Assist in regulatory inspections, audits, and compliance checks.
- Review and proofread product labels, artwork, and promotional materials.
- Keep up to date with regulatory changes in Sri Lanka market.
Qualification
- Bachelor’s Degree in Pharmacy (B. Pharm) or equivalent from a recognized institution.
- Valid registration with the Sri Lanka Medical Council (SLMC) or eligible for registration.
- 1–3 years of experience in a regulatory affairs role (preferably in a pharmaceutical or medical device company).
- Familiarity with NMRA guidelines and pharmaceutical documentation standards.
- Proficiency in Microsoft Office tools and good documentation practices (GDP).
- Strong communication skills, attention to detail and organizational ability.
Send us your CV! [email protected]
