LAVORO MASTER REGULATORY AFFAIRS TIROCINIO PARMA, EMILIA ROMAGNA

Who we are looking for main responsibilities will be responsible for conducting comprehensive reviews of adverse event reports for investigational and post-marketed...

It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, chemical manufacturing and controls, drug...

O produce and review global pricing material (ppt, word) for pricing procedures, guidelines and training o represent gva in cross-functional project teams o monitor...

Cro management experience required at least 5-year experience on inhalation products and/or biological drug products education master degree or phd in chemistry...