Global Regulatory Affairs Lead — FDA/EMA Submissions

A leading biotechnology firm in Turbigo, Italy, seeks a Senior Regulatory Affairs Specialist to oversee submissions to regulatory agencies like FDA and EMA. The role demands at least 5 years in regulatory affairs and fluency in English. Responsibilities include developing submission content and timelines, ensuring compliance with regulatory requirements, and managing interactions with internal teams and authorities. This position offers a contract and salary based on experience, promoting diversity and inclusion in recruitment.
#J-18808-Ljbffr