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
Job title: Packaging Engineer Location: Scoppito, Italy About the job As Packaging Engineer within our Packaging Team, you’ll deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for
Scope of the role This position is responsible for defining and executing global regulatory strategies for Chemistry, Manufacturing, and Controls (CMC) across the product lifecycle. It ensures robust regulatory CMC strategies, submission generation, compliance, and alignment with global
Experteer Italy is seeking an experienced project manager to serve as the operational hub for CMC project teams in Milano. You will manage day-to-day activities, ensuring quality and alignment with regulatory milestones. The ideal candidate has at
Overview In this role you will serve as the operational hub for CMC project teams, guiding day‑to‑day management of CMC development and tech transfer efforts within the Life Sciences and Healthcare unit. You collaborate with multidisciplinary teams and
Experteer Italy is seeking a Regulatory Affairs Specialist to manage CMC dossier preparations and submissions worldwide. This role involves working with cross-functional teams to translate technical reports into regulatory documents and ensuring compliance with GMP, ICH, EMA,
Experteer Overview In this role you drive the preparation and management of CMC dossiers for regulatory submissions worldwide. You work with cross‑functional teams to translate technical reports into submission‑ready Module3 content and assess regulatory impact of changes.
Alfasigma S.p.A. is seeking a highly experienced professional for a key role in defining global regulatory strategies for Chemistry, Manufacturing, and Controls (CMC). The ideal candidate will have over 15 years of regulatory experience with a deep
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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
Experteer Italy is looking for a Regulatory CMC Specialist to manage CMC regulatory activities within Chiesi’s Global Rare Diseases portfolio. This role requires collaboration with various teams to ensure compliance and timely deliverables. The ideal candidate will have
With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro
A global pharmaceutical company is seeking a Regulatory Affairs CMC Specialist to manage the preparation of regulatory submissions. The successful candidate will have over 3 years of experience in CMC regulatory affairs, demonstrating expertise in writing Module 3
A global pharmaceutical company in Turbigo is seeking a Regulatory Affairs CMC Specialist to manage dossier preparations for regulatory submissions. This role requires a degree in chemistry, pharmacy, or biotechnology, and at least 3 years of experience
With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro
Experteer Italy is seeking a Regulatory CMC Lead to define and execute global regulatory strategies for CMC across product life cycles. This role will involve collaboration with global health authorities and alignment of CMC regulatory approaches. The ideal candidate
Experteer Italy is seeking a Regulatory CMC Lead to define and execute global regulatory strategies for CMC across product life cycles. This role will involve collaboration with global health authorities and alignment of CMC regulatory approaches. The ideal candidate
Experteer Overview As Regulatory CMC Lead at Alfasigma, you define and execute global regulatory strategies for CMC across product life cycles. You will influence development, registration, and lifecycle management, collaborating across functions to align with product strategies. You
Scope of the role This position is responsible for defining and executing global regulatory strategies for Chemistry, Manufacturing, and Controls (CMC) across the product lifecycle. It ensures robust regulatory CMC strategies, submission generation, compliance, and alignment with global
Alfasigma S.p.A. is seeking a highly experienced professional for a key role in defining global regulatory strategies for Chemistry, Manufacturing, and Controls (CMC). The ideal candidate will have over 15 years of regulatory experience with a deep