At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Officer to join our team. This position is based in Athens, Kryoneri.
Main duties and responsibilities:
- Understanding of Regulatory strategy and documentation requirements.
- Act as responsible Regulatory Team member for assigned regulatory projects.
- Preparation of documentation for National phase of EU DCP/MRP/National procedures within assigned timelines.
- 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.
Requirements
Experience, skills and qualifications required:
- BSc Degree in Pharmacy, Biology or relevant field.
- 1-2 years of experience in Regulatory Affairs .
- Fluent in English and good MS Office skills.
- Strong organization skills, multi-tasking and able to meet deadlines.
- Effective communication and relationship management.
- Ability to work under pressure, resilience.
Benefits
The Company offers competitive remuneration, continuous learning and development opportunities, and a friendly and challenging working environment.
Other open roles at Demo S.A.(6)
DEMO Pharmaceuticals is an international industrial and commercial organization focused on the development, production and marketing of pharmaceutical products.
Key team members

Vassilis Dellopoulos

Theodora Kassa, ΜΒΑ

Barbara Mouzopoulou

Vassilis Floros
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