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
Chi cerchiamoprofessionista con master in scienze della vita o farmacia.5‑7 anni di esperienza internazionale in farmacovigilanza, settore farmaceutico, biotecnologico o cro.eccellenti capacità comunicative, negoziali e di leadership.competenze nella gestione di contratti e progetti complessi.conoscenza approfondita di
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 Group cerca una figura di Head of Incoming Materials QC presso lo Stabilimento di Parma San Leonardo. Ruolo a tempo indeterminato con responsabilità end-to-end sull’unità Incoming Materials del QC Chimico, incluse attività analitiche e gestione documentale. È
Questa posizione è in Chiesi Group_disabled Il processo di selezione sarà interamente gestito Chiesi Group_disabled. Ecco cosa farai La posizione, a tempo indeterminato, è inserita nel Controllo Qualità Chimico dello Stabilimento di Parma San Leonardo. LHead
Who we are looking for This is what you will do Support the provision to Chiesi Governance Bodies and Senior Management with robust, data‑driven insights and long‑term projections to enable informed decision‑making and maximize business value
Are you ready to shape the future of sustainable industries?Join GEA and become part of a global team that’s driving innovation, excellence, and impact across the food, beverage, and process sectors.GEA is one of the leading
This is what you will do Carry out pharmacovigilance (PV) operations (OPS) activities in interventional clinical trials sponsored either by GCD or GRD functions by maintaining up-to-date processes for safety-related aspects of interventional clinical trials, to