R&D GRAPS Affiliate and Partnership Oversight Unit Head Location: Parma, IT Responsibilities Assure that relationships with Partners and Affiliates are duly managed in the light of patient safety related matters and regulations both at global and
Chiesi Global Rare Diseases is seeking a Principal Regulatory Writer based in Italy to author, review, and manage regulatory documents for global submissions. You will coordinate cross-functional teams, ensure eCTD compliance, and supervise external writers to meet
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