Alfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100 markets spanning Europe, North and South
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
Date: 10 Feb 2026 Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Europe, IT Senior Manager, CMC Regulatory Affairs, Global Rare Diseases About us Chiesi is
A leading biopharmaceutical group is seeking a Senior Manager in CMC Regulatory Affairs to support their Global Rare Diseases portfolio. The role requires extensive Regulatory CMC experience, particularly in Biologics, along with leadership in maintaining regulatory documents and
Scope of the role This position is responsible for defining and executing global regulatory strategies for Chemistry, Manufacturing, and Controls (CMC) across the product lifecycle. It ensures robust regulatory CMC strategies, submission generation, compliance, and alignment with global
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Chiesi is an international research-focused biopharmaceutical
Experteer Overview As Regulatory CMC Lead at Alfasigma, you define and execute global regulatory strategies for CMC across product life cycles. You will influence development, registration, and lifecycle management, collaborating across functions to align with product strategies. You will
Head of Biologic Drug Substance - Process & Analytical Development Date: 30 Apr 2026 Department: GTD Global Technical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us
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 Italy is seeking a Head of Biologic Drug Substance Process and Analytical Development. In this role, you will define and drive the CMC strategy for biologics from research to launch, ensuring compliance and technical excellence.Ideal candidates will
Experteer OverviewIn this role you will author, review, and manage regulatory documents that translate clinical, nonclinical, and CMC data into compliant submissions for global authorities. You will serve on cross‑functional teams to ensure scientific rigor and regulatory
Purpose Of The JobThe Technical Marketing Manager acts as the bridge between technical operations and commercial teams, translating CDMO capabilities into compelling, credible value propositions for customers. The role supports lead generation, opportunity development, and strategic positioning
Chiesi Farmaceutici S.p.A. is seeking a Head of Biologic Drug Substance - Process & Analytical Development in Parma, Italy. This critical leadership position involves defining the strategy for biologics CMC development and overseeing drug substance processes. The ideal candidate