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
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
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
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
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 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.
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:
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
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
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
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 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
Sei pronto per entrare a far parte di una società di consulenza leader mondiale nellindustria farmaceutica e dei Medical Device ? PQE Group è affermata in questo settore dal 1998 , garantendo una presenza internazionale grazie
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
Experteer Overview In this role you will author, review, and manage regulatory documents that translate clinical, nonclinical, and CMC data into compliant submissions for global authorities. You will serve on cross‑functional teams to ensure scientific rigor and
Purpose Of The Job The Technical Marketing Manager acts as the bridge between technical operations and commercial teams, translating CDMO capabilities into compelling, credible value propositions for customers. The role supports lead generation, opportunity development, and strategic
Randstad Professional Italia is seeking an Interim Project Manager for an R&D pharmaceutical development program in Milan. Reporting to the CSO, you will lead late-stage development activities and coordinate cross-functional teams across Regulatory, CMC, Nonclinical, and Manufacturing to ensure
The Interim Management Division of Randstad Professional, specialized in the search and selection of Middle & Senior Management profiles, is looking for on behalf of a leading corporation one professional profile of: INTERIM PROJECT MANAGER, R&D
Principal Regulatory Writer, Global Rare Diseases Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT What we are looking for This is what you