Regulatory Affairs Post-approval Senior Officer
4 weeks ago
Athens, Attica, Ελλάδα
DEMO Pharmaceuticals S.A.
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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 (Non-EU markets) to join our team. This position is based in Athens, Kryoneri.
Responsibilities:
• Understanding of Regulatory strategy and documentation requirements in Non-EU markets ( Middle East, Africa, Asia, CIS, LATAM)
• 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
• 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 international regulatory authorities, local agents, and distributors
• 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 demonstrated experience managing regulatory submissions in Non
- EU markets ( Middle East, Africa, Asia, CIS, LATAM)
• 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.
Responsibilities:
• Understanding of Regulatory strategy and documentation requirements in Non-EU markets ( Middle East, Africa, Asia, CIS, LATAM)
• 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
• 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 international regulatory authorities, local agents, and distributors
• 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 demonstrated experience managing regulatory submissions in Non
- EU markets ( Middle East, Africa, Asia, CIS, LATAM)
• 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.