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
Overview The Scientist will lead and support research and development projects focused on food applications, ensuring the highest standards in laboratory practices, analysis, and scientific assessment. The role requires at least 5 years of relevant experience,
We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine
Teoresi S.p.A. , 35+ anni di storia , 8 società tra Italia, Stati Uniti, Germania, Svizzera, +1200 risorse, 4 acquisizioni in un anno, 1 solo partner ed un’unica soluzione. Per ampliamento di un Team operante nel
Chiesi Farmaceutici S.p.A. is seeking a QA Validation & Equipment Compliance Manager in Parma. This role focuses on ensuring quality oversight and compliance with regulatory requirements, managing departments operational efficiency and safety.Ideal candidates will have a scientific
Unazienda di consulenza sta cercando un professionista per gestire la documentazione di qualifica in ambito GxP. Il candidato ideale deve avere almeno 2 anni di esperienza in ruoli similari e conoscenze delle normative GxP. Si occuperà
Akkodis cerca un Project Technician nella divisione Life Sciences a Parma. I candidati devono avere un diploma tecnico e esperienza con GMP, P&ID e schemi elettrici. Offriamo un contratto a tempo indeterminato con RAL a partire
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. You
Experteer OverviewIn this role you act as the global technical reference for Respiratory, Orals & Small Molecules, ensuring robust, compliant manufacturing tech throughout the product lifecycle. You’ll contribute to industrialization strategies within R&D Product Teams and
Chiesi Farmaceutici S.p.A. is seeking a Subject Matter Expert for Process Validation in Parma, Italy. In this role, you will support industrialization and lifecycle management for various pharmaceutical products.The successful candidate will need a Bachelors degree in
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 delle
Teoresi S.p.A. — oltre 35 anni di storia, 8 sedi tra Italia, Stati Uniti, Germania e Svizzera, più di 1200 persone, 4 acquisizioni nell’ultimo anno, un unico partner e una sola soluzione. Per ampliamento di un
Chiesi Farmaceutici S.p.A. is seeking a Subject Matter Expert for Process Validation and technical maintenance activities in Parma, Italy. Youll support industrialization and technology transfer for respiratory, oral, and small molecule products, ensuring compliant manufacturing processes. The
Teoresi S.p.A. , 35+ anni di storia , 8 società tra Italia, Stati Uniti, Germania, Svizzera, +1200 risorse, 4 acquisizioni in un anno, 1 solo partner ed un’unica soluzione. Per ampliamento di un Team operante nel
Chiesi Group in Parma is seeking an experienced quality assurance professional to oversee validation and qualification activities. The ideal candidate has 8-10 years in the pharmaceutical sector, specializing in regulatory compliance, and team management. The role involves
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
Experteer Overview In this role, you provide quality oversight for qualification and validation activities, ensuring regulatory compliance and data integrity across GMP manufacturing. You will lead the site Validation Program and oversee CSV governance to guarantee products meet
Experteer Italy is looking for a qualified professional to provide quality oversight for qualification and validation activities. This role involves leading the Validation Program and ensuring compliance with GMP standards across manufacturing. The ideal candidate has 8-10 years
Experteer Overview In this role you act as the global technical reference for Respiratory, Orals & Small Molecules, ensuring robust, compliant manufacturing tech throughout the product lifecycle. You’ll contribute to industrialization strategies within R&D Product Teams
Overview The Scientist will lead and support research and development projects focused on food applications, ensuring the highest standards in laboratory practices, analysis, and scientific assessment. The role requires at least 5 years of relevant experience,