Dr. Chloé Ravier

Managed following processes in accordance with ISO 13485 and MDR: - Documentation management (GDP) - Computer Software Validation (GAMP5) - Risk assessment for processes and systems (FMEA) Led following projects: - Implementation of the company's DMS - Accreditation of the intern testing laboratory (ISO 17025)

Assessment and improvement of the compliance to EU GMP of a new biotechnology production line

Took part in the pharmacy activities such as: - narcotic drugs delivery - help in the chemotherapy preparation process - manufactured extamporaneous preparations - helped with daily advice to nurses and clinicians

Took part in the therapeutical education of kidney transplanted patients

Project: Industrialisation of a new biotechnological injectable drug - Studied and created an operating procedure for the reprocessing of a biotechnological drug - Wrote a regulatory document - Conducted studies and wrote study reports

Delivered prescriptions Advised costumers about medicines and hygiene product Out-of-date and stock management Teamwork

Receptioned Orders Delivered prescriptions Advised costumers about medicines and hygiene products Out-of-date and stock management Teamwork