At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Post-approval 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
• 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.

• BSc Degree in Chemistry, Biology or relevant field.
• 1-2 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

The company offers competitive salary and benefits, continuous specialized training, career development and a friendly working environment.