Amira Akchiche

Manager of Regulatory Affairs, in Corporate structures of pharmaceutical companies, primarily focused on EU/US/International Drug Development and Registration activities, having also encompassed all aspects of Life Cycle Management for Medicinal Products and Medical Devices.

Has worked on drug products at international level, with quick identification of scientific, regulatory, and business issues.

Long standing communication and Functional practice acquired on site with Manufacturing & Controls, Non-clinical, Clinical, Quality Assurance, International Departments, affiliates and distributors beyond necessary knowledge of relevant Regulations for such functions.

Planning and organizational skills, strategy and execution-driven at same time. Ease with cross-functional matrix working environment.

Customer needs and solutions orientated, team-spirit driven. Leadership skills with abilities to mix and develop talents in a group. Ease with top management level and multicultural communication.