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
Specialista QA Validation - Supporto Attività di Review Tipo di Impiego: Full Time Descrizione del ruolo: La risorsa sarà inserita nel team QA Validation con il compito di supportare le attività di review e pre-approvazione delle
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
Overview The Scientist will lead and support research and development projects focused on food applications, ensuring the highest standards in laboratory practices, analysis, and scientific assessment. The role requires at least 5 years of relevant experience,
Experteer Overview In this role you lead and support R&D projects focused on food applications, ensuring rigorous lab practices and scientific assessment. You work within a cross‑functional setting to advance product safety, quality, and shelf‑life through
Principal Regulatory Writer, Global Rare Diseases Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT What we are looking for This is what you
The resource will support logistics management and distribution processes for sales products. Main Activities: Support in the operational management of shipments (national and international). Monitoring the performance of external suppliers and internal flows (KPIs). Collaboration with
Experteer Overview In this role you ensure GCP compliance across Global R&D by managing CAPAs, quality metrics, and audit programs. You will drive the documentation and process controls that support audit readiness and supplier qualification. You