Regulatory Affairs Consultant M/F – 996

Pharma D&S (a ProductLife Group Company) is urgently looking for a Regulatory Affairs Consultant to join their teams in Milan (Cassina de’ Pecchi), Italy. Quality documents preparation and writing (module 2.3 and 3) Preparing the application for filing an Active Substance Master File (ASMF) Variation and renewal of AIC Documentation storage Support for internal and external inspections Preparing specific SOP Communicating with Regulatory Authorities Education Scientific Bachelor’s Degree. A Master’s Degree in Regulatory Affairs is a plus. Experience At least 2-3 years of experience in RA in a Pharmaceutical Company or Service Provider Skills Fluent English is required Good interpersonal skills Excellent organizational skills and time management Knowledge of regulations and guidelines Willingness to travel About us Pharma D&S (a ProductLife Group Company) is a Pharmaceutical and Lifesciences Consulting firm able to provide timely, efficient and high quality services in: Quality & Process, Regulatory Affairs, Pharmacovigilance and Clinical Studies. J-18808-Ljbffr