At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Post-approval Senior Officer to join our team. This position is based in Athens, Kryoneri.
Responsibilities:
- Understanding of Regulatory strategy and documentation requirements
- Act as responsible Regulatory Team member for assigned regulatory projects
- Assist and support the junior personnel of the team for the projects they have undertaken
- Preparation of module 1 documentation for DCP, MRP, RUP and National applications in line with assigned timelines for out-licensing and in-licensing products in EU countries
- Collect, prepare, compile regulatory documentation, for the product’s lifecycle maintenance (administrative, quality, safety variations and renewal procedures).
- Compile and monitor the progress of scientific responses to deficiencies raised by the Regulatory authorities
- Liaise with external Regulatory authorities as required.
- Ensure policies and procedures are properly understood, evaluated and carried out. Make sure modifications are investigated if necessary.
- Liaise with various departments to collect all necessary information and documentation, in accordance with defined guidelines for Pharmaceutical Dossier submission and product registration
- Support internal activities of Regulatory department in order to ensure regulatory compliance of registered products
- Preparation of submissions including CMC variation filling.
Requirements
- BSc Degree in Chemistry, Biology or relevant field.
- 2-4 years of experience in Regulatory Affairs / CMC within a Pharmaceutical organization.
- Fluent in English and good MS Office skills
- Good command of eCTD software and CESP platform.
- Strong organization skills, multi-tasking and able to meet deadlines
- Effective communication and relationship management
- Knowledge of EU and global regulatory guidelines
- Ability to work under pressure, resilience
Benefits
The company offers competitive salary and benefits, continuous specialized training, career development and a friendly working environment.
