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
Chiesi Farmaceutici S.p.A. is seeking a Quality Assurance professional based in Parma, Italy. The role involves ensuring GCP compliance within clinical project teams and responsibilities such as reviewing study documents and managing GCP inspections. Candidates should have
Experteer Overview In this role you drive GCP compliance within clinical development, acting as a QA reference for project teams. You’ll implement and maintain the quality system in GCP areas and support study design, execution, and reporting. You
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:
Global R&D QA, Senior Validation, Digital & Data Integrity Specialist Date: 22 Jul 2026 Department: Global R&D Quality Assurance Business Area: Quality Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Chiesi is an
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
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:
Experteer Overview In this Senior GDP QA Specialist role, you will own key GDP QA activities in a dynamic pharmaceutical setting, ensuring regulatory compliance and business continuity. You will manage core quality processes and drive risk‑based decisions to