About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a
Part of a highly successful global corporation, our client is a name synonymous with the best in the industry. A true innovator who have experienced substantial and consistent success for many years, they design and manufacture
Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT Principal Regulatory Writer, Global Rare Diseases Chiesi is an international research-focused biopharmaceutical group with 90
Experteer Overview In this role you will develop regulatory strategies for EU and international markets for Chiesi Global Rare Diseases. You will coordinate regulatory submissions and provide guidance on regional requirements to support product development and expansion.
What we are looking for Reporting to the Lead, EU & Int’l Regulatory Affairs, Global Rare Diseases, the Manager, EU & International Regulatory Affairs develop regulatory strategies for EU & International markets to meet Chiesi Global