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
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 seeks a candidate to author and manage regulatory documents that translate data into compliant submissions. This role involves overseeing document development for marketing applications and guiding both external writers and internal experts. The ideal candidate will
Experteer Overview In 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
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 years’
Chiesi Farmaceutici S.p.A. is seeking a Principal Regulatory Writer for their Global Rare Diseases department in Parma, Italy. This role involves managing regulatory documents for global health authorities, ensuring compliance and quality throughout the drug development lifecycle. The
Technical Writer – Automotive After Sales Documentation Specialist*High competence and the passion for new challenges make our Electrics/Electronics division the guidepost to the automotive future. Take your next step and support our team.We are looking for Automotive
Chiesi Farmaceutici S.p.A. is seeking a Principal Regulatory Writer for their Global Rare Diseases department in Parma, Italy. This role involves managing regulatory documents for global health authorities, ensuring compliance and quality throughout the drug development lifecycle. The
Please submit your CV in English and indicate your level of English proficiency. Mindrift connects specialists with project-based AI opportunities for leading tech companies, focused on testing, evaluating, and improving AI systems. Participation is project-based, not
A leading technology consulting firm in Italy seeks professionals for project-based AI opportunities focused on testing and improving AI systems. Responsibilities include reviewing coding tasks, writing functional tests, and analyzing AI performance. Ideal candidates have a
Questa posizione è in Chiesi Group. Consulti la panoramica del ruolo qui sotto. Se è sicuro/a di possedere le giuste competenze ed esperienze, si candidi oggi stesso. Riassunto dellopportunità da parte di Joinrs AI: Chiesi Group
Questa posizione è in Chiesi Group Riassunto dellopportunità da parte della Joinrs AI : Chiesi Group ricerca un Global Pharmacovigilance Medical Safety Writer con almeno 1 anno di esperienza in farmacovigilanza e laurea magistrale in scienze o
Questa posizione è in Chiesi Group Riassunto dellopportunità da parte della Joinrs AI : Chiesi Group cerca un Principal Regulatory Writer con laurea in scienze della vita (PhD o Pharm. D preferibili) per supportare il team Regulatory
Chiesi Farmaceutici S.p.A. is looking for a Global Pharmacovigilance Medical Safety Writer in Parma. This temporary position involves developing pharmacovigilance documents, supporting global planning for molecules, and ensuring compliance with safety reporting standards. Ideal candidates should have
Global Pharmacovigilance Medical Safety Writer - Temporary Date: 28 Apr 2026 Department: Global Regulatory Affairs & Patient Safety Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Temporary Location: Italy (Parma) with possibility
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 years’
Technical Writer – Automotive After Sales Documentation Specialist* High competence and the passion for new challenges make our Electrics/Electronics division the guidepost to the automotive future. Take your next step and support our team. We are looking
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:
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