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
Responsible for the implementation and the optimization of robust manufacturing processes in Production ensuring that safety, effectiveness, quality and reliability of the devices are met. Lead PFMEA activities in coordination with other stakeholders. Generate and validate
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:
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
Azienda biomedicale orientata allinnovazione tecnologica finalizzata al miglioramenti dei processi di trapianti di organi seleziona un Ingegnere di produzione che sarà responsabile dellimplementazione e dellottimizzazione di processi di produzione, garantendo la sicurezza, lefficacia, la qualità e
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
Business Area: R&D, Pharmacovigilance & Regulatory Affairs 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
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
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
On behalf of our Client, Chiesi Farmaceutici , one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a
On behalf of our Client, Chiesi Farmaceutici , one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a
Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Temporary Location: Parma, IT This is what you will do Accountable for coordination of the operational management of assigned projects in order to
Chiesi Research & Development is seeking a Clinical Trials Manager to coordinate the operational management of assigned projects, ensuring development of compounds in line with Chiesi’s goals and medical/scientific standards. Responsibilities Accountable for coordination of the
Sei un* Content creator e vuoi unirti al nostro team? Questa è una posizione aperta: stiamo cercando attivamente una nuova figura da inserire nel team. Se ti riconosci in questa descrizione, inviaci CV e portfolio —
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
Sei un* Content creator e vuoi unirti al nostro team? Questa è una posizione aperta: stiamo cercando attivamente una nuova figura da inserire nel team. Se ti riconosci in questa descrizione, inviaci CV e portfolio —
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
On behalf of our Client, Chiesi Farmaceutici , one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a
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