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
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 affiliates
Global Technical Operations & Supply (Global Tech Op&S) is Chiesi’s global manufacturing and supply area, responsible for ensuring consistent, outstanding quality, service and value across our end‑to‑end supply chain. Global Tech Op&S oversees the entire lifecycle of the drug: from
Experteer Overview In this role you will develop regulatory strategies for EU and international markets for Chiesi Global Rare Diseases. You will coordinate regulatory submissions and provide guidance on regional requirements to support product development and expansion.
Regional Sales Manager: Europe Location: Madrid, Barcelona, Berlin, Krakow, Paris, Budapest (or another major hub city in the region with regular travel required) Employment Type: Full-time About Us MLA – Move Language Ahead, trading as Go Languages
Turner & Townsend is a global professional services company with over 22,000 people in more than 60 countries. Working with our clients across real estate, infrastructure, energy and natural resources, we transform together delivering outcomes that improve
Part of a highly successful global corporation, our client is a name synonymous with the best in the industry. A true innovator who have experienced substantial and consistent success for many years, they design and manufacture a
Overview In this role you will carry out pharmacovigilance (PV) operations for interventional clinical trials, ensuring compliant, high-quality safety data and up-to-date processes. You’ll work with global teams and CROs to support PV requirements across R&D assets.
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
Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Italy, IT Responsibilities End to end execution of assigned innovation and initiatives, translating strategies and study designs on time, quality, and
Experteer Overview In this role you will oversee external manufacturing partners to ensure reliable product availability for global markets while balancing service, inventory, and cost. You will lead a cross-functional team and act as the main interface
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
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 person
Business Area: R&D, Pharmacovigilance & Regulatory Affairs 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
Who we are looking for This is what you will do End to end execution of assigned innovation and initiatives, translating strategies and study designs on time, quality, and compliant delivery across programs, therapeutic areas and
Turner & Townsend is a global professional services company with over 22,000 people in more than 60 countries. Working with our clients across real estate, infrastructure, energy and natural resources, we transform together delivering outcomes that improve
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,
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
Questa posizione è in Chiesi Group Il processo di selezione sarà interamente gestito Chiesi Group. Head of Clinical Project Management Data: 24 Jun 2026 Department: Global Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type:
This is what you will do An experienced Clinical Operations Lead with a strong background in global drug development, capable of providing strategic and operational leadership across complex clinical development programs. The Clinical Operations Lead (COL) ensures