Alfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100 markets spanning Europe, North and South
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
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
Director – Regulatory CMCAre you a CMC regulatory expert with experience across product development, submissions, and lifecycle management? This is an opportunity to lead on CMC regulatory strategy for a biopharma organisation advancing innovative therapies across multiple modalities.Scopra esattamente
ID: 2333 Date of Posting: Feb 24, 2026 Business Area: Regulatory Affairs Job Type: Direct Employee Territory: Full-Time or Part-Time: Full Time Seniority: Mid-senior With its beginnings in a family run pharmacy in Correggio, Italy in
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.
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 Overview In this role you will support manufacturing and global operations focused on delivering high-quality medicines. You will work with cross‑functional teams to improve processes and validate analytical methods, ensuring GMP compliance across the value
In questa posizione, entri a far parte della divisione Intralogistics di CMC Industries per guidare lo sviluppo commerciale e la soddisfazione del cliente. Lavora a stretto contatto con i clienti esistenti per consolidare relazioni e promuovere servizi
Experteer Overview Senior Regulatory Affairs CMC Specialist to lead preparation of Module 3 dossiers and drive regulatory strategies for worldwide submissions. You will work with cross-functional teams to translate technical data into regulatory documents, assess gaps, and
Director – Regulatory CMC Are you a CMC regulatory expert with experience across product development, submissions, and lifecycle management? This is an opportunity to lead on CMC regulatory strategy for a biopharma organization advancing innovative therapies across multiple modalities. The
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 external
Experteer Overview As Head of Biologic Drug Substance Process and Analytical Development, you will define and drive the CMC strategy for biologics from research to launch. You will lead the Drug Substance process and analytical development, ensuring compliance, scaling,
Siamo alla ricerca di un/a Formulatore R&D con esperienza da inserire nel nostro team di sviluppo farmaceutico presso il sito di Bollate (MI). La risorsa sarà coinvolta nello sviluppo di nuove formulazioni farmaceutiche e nel supporto
Overview This position is responsible for defining and executing global regulatory strategies for Chemistry, Manufacturing, and Controls (CMC) across the product lifecycle. This role ensures robust regulatory CMC strategies, submission generation, compliance, and alignment with global health authority
Siamo alla ricerca di un/a Formulatore R&D con esperienza da inserire nel nostro team di sviluppo farmaceutico presso il sito di Bollate (MI).La risorsa sarà coinvolta nello sviluppo di nuove formulazioni farmaceutiche e nel supporto tecnico
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 will
Department: Global Operations & Production Job ID: 45181 Our people in Manufacturing & Global Operations share two priorities: getting things done and making things better. If you’re a dynamic person with a positive mindset, you’ll fit
Sia is seeking a CMC Technical Project Manager to oversee CMC development and technical transfer projects. This role demands strong communication skills and experience in project management within the biopharmaceutical sector. The ideal candidate will have at least 2