Company DescriptionSia is a next-generation, global management consulting group born digital, augmented by data, enhanced by creativity, and driven by responsibility. We partner with clients to resolve challenges and capitalize on opportunities. We believe that in today’s
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
Overview As Senior Process Scientist, you will drive the development and manufacturing oversight of LNP-based gene therapy programs within Chiesi Global Rare Diseases. You’ll lead formulation development, screening, and process optimization, partnering with external CROs/CDMOs and internal CMC teams
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join our global Regulatory Affairs team in a client-dedicated role supporting commercial medicinal products used in clinical trials, including comparator and auxiliary medicinal products. This highly client-facing position combines
Area Iberia, Italy & Malta is part of DNV Maritime, Region West Europe.The Area includes all maritime business activities and consists of ~60 employees in 11 locations.The Area operates with two Service Lines: Newbuilding and Certification-Verification of
Fondazione Telethon (FT) is a leading biomedical charity committed to advancing research into tangible therapeutic options for people living with rare genetic diseases. Through its affiliated research institutes – TIGEM (Naples) and SR-TIGET (Milan) – FT
Fondazione Telethon is a major Italian charity focused on rare genetic diseases. Founded in 1990, its mission is to advance biomedical research towards the cure of genetic diseases with the ultimate goal of making new therapies
Overview As Global NPP Manager, you drive early pipeline assessment and inorganic growth initiatives for the AIR Franchise. You analyze market landscapes, competitive dynamics, and revenue potential to shape investment stories and commercial strategies. You work
Overview In this role you drive analytical development for gene editing and nucleic acid-based therapeutics within the GRD CMC team. You lead method development and control strategies for complex modalities, including ATMPs and LNP-based products, collaborating across functions from
Overview In this role you lead R&D programs by developing integrated development plans and coordinating cross-functional teams to drive drug development programs forward. You will align Preclinical, Safety, Regulatory, Clinical Operations, and CMC activities, ensuring timely delivery within agreed
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Regulatory Affairs Manager As a Regulatory Affairs Manager, youll offer innovative solutions, including regulatory affairs expertise and client interface, to provide strategic regulatory intelligence and
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Director Project Management – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750