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The role will provide scientific and technical leadership for analytical development at various stages of drug development both internal and external through CDMO with particular emphasis on research and early development (pre-DP0) including material
You will ensure that our suppliers and external partners meet the highest quality and compliance standards - while enabling innovation, efficiency, and sustainable growth. You’ll operate as a key expert within our Quality organization, influencing
You will be responsible for activities related to chemical intermediates, payload linkers, and drug linkers used in ADC development at Genmab’s partnered CMOs. You will work across project teams to support the CMC Project Managers and collaborate
Responsible for formulation and process development activities from early development through scale-up, validation, and technology transfer. The role requires a high level of technical expertise, independent decision-making, cross-functional leadership,
This role carries full accountability for all Quality Assurance and Commissioning & Qualification (C&Q) activities across the entire project lifecycle, from conceptual design through Process Performance Qualification (PPQ) and final regulatory approval.