Job Description
WE ARE HIRING!
YOU ARE THE MISSING PIECE...
EXECUTIVE REGULATORY AFFAIRS
YOUR ROLE WILL INVOLVE
- Prepare and submit regulatory dossiers for product registrations and certifications.
- Liaise with regulatory authorities and manage application follow-ups.
- Track submissions, renewals, and regulatory expiries.
- Coordinate GMP audits, inspections, and certifications.
- Support validation, qualification, and regulatory documentation.
- Maintain relationships with regulatory bodies and industry stakeholders.
- Monitor regulatory updates and ensure compliance.
REQUIRED QUALIFICATIONS
- SLMC Registered pharmacist with certificate (Professional certification/ diploma/ degree in Pharmacy) is an advantage.
- Minimum 1-2 years of hands-on experience in regulatory roles, preferably in a healthcare or pharmaceutical manufacturing environment.
- Understanding of regulatory requirements across surgical, pharma, and wellness product categories (Specially for Medical Devices).
- Exceptional attention to detail, particularly in documentation and legal submissions.
HOW TO APPLY
Send your CV to: career@sisiliprojects.com
Manager - Human Resources, Sisili Projects Consortium Pvt Ltd, No. 118/A, Barnes Place, Colombo 07
Tel: +94-112-576050 / +94-76-549-5144
E-mail: career@sisiliprojects.com