About usChiesi 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 singular
About usChiesi 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 singular
About usChiesi 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 singular
GRAPS Patient Safety Operations, Post Marketing Manager – Chiesi – Vicofertile, Emilia‑Romagna, Italy About Chiesi Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases Chiesi Parma, Emilia-Romagna, IT 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,
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 singular purpose:
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
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
Chiesi seeks a Regulatory Affairs (RA) Senior Manager with strong CMC pre/post-approval experience to support the Global Rare Diseases portfolio. You will lead CMC documentation, author sections, and advise on regulatory strategies across global submissions. The role