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
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
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
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
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 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
McDermott Laboratories Limited Key responsibilities for this role include: Support effective global Project Team meetings that provide a forum for communication, removing obstacles and resolving issues. Ensure meeting deliverables and agreements are carried out. Lead the
CLIENT ROLE This is a highly visible, global role responsible for aligning technical, clinical, regulatory, industrialization and commercial priorities to rapidly deliver impactful and innovative therapeutic solutions to patients worldwide. - Reporting to Global Operations Strategy
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
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 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
Providing hands‑on scientific and technical leadership in process insourcing, technology transfer, scale‑up, and validation activities Coordinating upstream process development, optimization, and industrialization activities with internal R&D teams and external CMOs Leading lifecycle management activities for commercial
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
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
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:
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