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 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:
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
Apply for Medical Assistant - Parma Office at Apex Skin in Parma, EMI, IT. This Full time on site position offers great opportunities for career growth. About Apex Skin We are Apex Skin, and our mission
Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Temporary Location: Parma, IT This is what you will do Accountable for coordination of the operational management of assigned projects in order to
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 About us Chiesi is an international research-focused
Chiesi Research & Development is seeking a Clinical Trials Manager to coordinate the operational management of assigned projects, ensuring development of compounds in line with Chiesi’s goals and medical/scientific standards. Responsibilities Accountable for coordination of the
We are seeking an experienced Proposal Manager to lead the preparation of technical and commercial proposals specifically for EPC Plant projects. You will manage the entire proposal lifecycle for complex engineering, procurement, and construction tenders, ensuring compliance
Select how often (in days) to receive an alert: Quality & Compliance System Senior Specialist Date: Apr 3, 2026 Department: Quality Operations Italy, Parma Site Job Type: Direct Employee Business Area: Quality Contract Type: Permanent Location:
Questa posizione è in Chiesi Group Riassunto dellopportunità da parte della Joinrs AI : Chiesi Group cerca un Corporate Quality Auditing Senior Specialist con laurea in discipline scientifiche come Farmacia, Chimica o Biologia. Il candidato sarà
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Questa posizione è in Chiesi Group Riassunto dellopportunità da parte della Joinrs AI : Chiesi Group cerca un QA Validation & Equipment Compliance Manager con laurea in discipline scientifiche o ingegneristiche. Il ruolo prevede la supervisione
Questa posizione è in Chiesi Group Riassunto dellopportunità da parte della Joinrs AI : Chiesi Group ricerca un Global Pharmacovigilance Medical Safety Writer con almeno 1 anno di esperienza in farmacovigilanza e laurea magistrale in scienze
Questa posizione è in Chiesi Group Riassunto dellopportunità da parte della Joinrs AI : Chiesi Group cerca un Senior Clinical Project Manager con una laurea in Scienze della Vita per gestire progetti clinici complessi nel settore
Questa posizione è in Chiesi Group Riassunto dellopportunità da parte della Joinrs AI : Chiesi Group cerca un Manager, EU & International Regulatory Affairs con una laurea in Scienze della Vita . Il candidato si occuperà
Questa posizione è in Chiesi Group Riassunto dellopportunità da parte della Joinrs AI : Chiesi Group cerca un Specialist, Labelling & Compliance Regulatory Affairs con laurea in scienze della vita o affini per supportare le attività
This is what you will do You will act as Subject Matter Expert for Process Validation and technical maintenance activities, supporting industrialization, product technology transfer and life cycle management for Respiratory, Orals & Small Molecules products.