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
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
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
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 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
A leading biopharmaceutical group is seeking a Senior Manager in CMC Regulatory Affairs to support their Global Rare Diseases portfolio. The role requires extensive Regulatory CMC experience, particularly in Biologics, along with leadership in maintaining regulatory documents 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 organisation advancing innovative therapies across multiple modalities.
Sei pronto ad entrare in una realtà internazionale che sta ridefinendo gli standard dell’industria farmaceutica e dei Medical Device? In PQE Group, la nostra divisione Regulatory Affairs è sempre in una fase di grande crescita grazie
Ti appassiona la contabilità e desideri affiancarti a professionisti esperti e trasformare la tua esperienza amministrativa in un profilo contabile completo? Grafton Office* è un team dedicato a valorizzare le esperienze, le competenze e il potenziale dei
Ti appassiona la contabilità e desideri affiancarti a professionisti esperti, consolidando le tue competenze a livello pratico? Grafton Office* è un team dedicato a valorizzare esperienze, competenze e potenziale dei candidati nei ruoli Accounting, Sales, Marketing,
Alfasigma is looking for a Regulatory Affairs professional specializing in Chemistry, Manufacturing, and Controls (CMC) to guide global strategies throughout the product lifecycle. With over 15 years of regulatory experience, you will ensure compliance with FDA, EMA,
Experteer Italy is seeking a Regulatory CMC Manager to drive regulatory activities for Chiesi Global Rare Diseases products. The role involves overseeing documentation, collaborating with teams for submissions, and shaping regulatory strategy across a global portfolio.The ideal
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
Chiesi Farmaceutici S.p.A. in Parma is currently seeking a Senior Manager for CMC Regulatory Affairs within their Global Rare Diseases unit. This role is critical for managing regulatory submissions across various markets for biopharmaceutical products. The ideal
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
Date: 10 Feb 2026 Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Europe, IT Senior Manager, CMC Regulatory Affairs, Global Rare Diseases About us Chiesi is
Sei pronto ad entrare in una realtà internazionale che sta ridefinendo gli standard dellindustria farmaceutica e dei Medical Device? In PQE Group, la nostra divisione Regulatory Affairs è sempre in una fase di grande crescita grazie
Sei pronto ad entrare in una realtà internazionale che sta ridefinendo gli standard dellindustria farmaceutica e dei Medical Device? In PQE Group, la nostra divisione Regulatory Affairs è sempre in una fase di grande crescita grazie