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
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 Research & Development Our R&D team represents a fundamental asset for the business. It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery technology,
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
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 timely
Department: Global R&D Quality Assurance Business Area: Quality Job Type: Direct Employee Contract Type: Permanent Location: Parma, Italy This Is What You Will Do Ensure the GCP compliance within the project teams, acting as QA reference
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT (role can be based in one of our
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:
R&D Process Excellence & Digital Solutions Senior Manager Department: Global R&D Strategy, Portfolio and Digital Develop Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Chiesi is
Experteer OverviewIn this role you will lead Environment, Health & Safety at the Parma plant, ensuring compliance and fostering a strong safety culture. You will partner with line managers to apply best practices, manage ISO 45001/14001 systems, and
OverviewExperteer OverviewIn this role you will support GRAPS to ensure the pharmacovigilance system aligns with regulatory expectations. Based at the Parma headquarters with hybrid work, you will help maintain PSMF readiness, monitor PV KPIs, and report on global
Department: Quality Operations Italy, Parma Site Job Type: Direct Employee Business Area: Quality Contract Type: Permanent Location: Parma, IT About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than
Overview Experteer OverviewIn this role you will support GRAPS to ensure the pharmacovigilance system aligns with regulatory expectations. Based at the Parma headquarters with hybrid work, you will help maintain PSMF readiness, monitor PV KPIs, and report on
This is what you will do To support GRAPS in ensuring that Companys pharmacovigilance system is consistent with the regulatory requirements in terms of structure and performances. You will be responsible for To evaluate relevant pharmacovigilance regulations, guidelines
Experteer Overview In this role you design and drive IT projects for manufacturing and purchasing, ensuring governance, quality, and timely delivery. You collaborate with global and regional partners, IT domains, and business stakeholders to implement secure,
Consolidated Financial Statement Senior Analyst We are looking for a Consolidated Financial Statement Senior Analyst within the Consolidated Financial Statement unit. The role will report to the Consolidated Financial Statement Senior Manager and it will be based
About Camlin Group: Camlin is a global technology leader with a bold vision: to bring revolutionary products to life across diverse industries like power and rail. Our passion extends to pioneering R&D projects in various scientific