About this role
Role Overview
- Prepare, review and update SOPs and other documents within the Quality Management System, ensuring compliance with national and international regulatory requirements;
- Responsible for transportation validation reports, ensuring that storage and distribution conditions maintain product integrity and quality;
- Support the management and control of regulatory documentation, audits, investigations of deviations and non-conformities, procedure training, and Good Manufacturing Practices.
Requirements
- Bachelor's degree in Pharmacy or a related field.
- Experience in regulatory affairs within the pharmaceutical industry.
- Fluent English, able to conduct meetings in English.