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
Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries,
Business Area R&D, Pharmacovigilance & Regulatory Affairs Job Type Direct Employee Contract Type Permanent Location Italy, IT About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries,
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
Experteer Overview In this role you will enhance reliability and continuous improvement of plant equipment across a four‑site network. You will support operational efficiency through proactive maintenance, repairs, and upgrades, collaborating with cross‑functional teams to sustain
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
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 work
Responsibilities Functions as a Lead Statistical Programmer, participates in SAS related programming activities for all clinical and safety data systems at Chiesi as well as activities in preparing data and metadata packages for regulatory submission. The
Questa posizione è in Chiesi Group_disabled Il processo di selezione sarà interamente gestito Chiesi Group_disabled. About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its
Experteer Overview As Corporate IT Auditor, you assess ATSs IT landscape to ensure data, processes, and systems are accurate, efficient, and secure, supporting the company’s objectives. You will design, test, and evaluate IT internal controls and lead