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
Experteer Italy is looking for a Regulatory CMC Specialist to manage CMC regulatory activities within Chiesi’s Global Rare Diseases portfolio. This role requires collaboration with various teams to ensure compliance and timely deliverables. The ideal candidate
Experteer Overview In this role you will support Chiesi’s Global Rare Diseases portfolio by managing CMC regulatory activities across submissions and lifecycle. You will collaborate with Core teams, GCST, and external CMOs to ensure compliance and
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:
Celltrion Group provides biosimilar and innovative biopharmaceutical medications to help increase patient access to advanced therapies around the world. Celltrion Group offers biologics to about 110 countries, along with more than 30 global partners around the world.
Jobtailor in Parma seeks an experienced bioprocess development leader to drive insourcing, tech transfer, and scale‑up of commercial biologics processes. You will coordinate upstream development with R&D and CMOs to ensure GMP compliance and lifecycle management. The
Providing hands‑on scientific and technical leadership in process insourcing, technology transfer, scale‑up, and validation activities Coordinating upstream process development, optimization, and industrialization activities with internal R&D teams and external CMOs Leading lifecycle management activities for commercial
Experteer Overview In this role you will coordinate training and documentation across the Global TechOps & Supply area to ensure GMP compliance and effective knowledge management. You will contribute to governance and implementation of the new
Experteer Italy is seeking a professional to coordinate training and documentation in the Global TechOps & Supply area based in Parma. You will ensure GMP compliance while improving knowledge management processes within a global biologics/pharma environment. The
Providing hands‑on scientific and technical leadership in process insourcing, technology transfer, scale‑up, and validation activities Coordinating upstream process development, optimization, and industrialization activities with internal R&D teams and external CMOs Leading lifecycle management activities for commercial
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
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
Purpose Of The Job The 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