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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
Provide end-to-end QA oversight of DP, IMP manufacturing activities internally and at CMOs, ensuring sustained GMP compliance and supply continuity for clinical trials. Ensure batch release within delegated authority in accordance with applicable GMP
You will lead and support new product introductions, major technology transfer activities, and product remediation initiatives, while ensuring process knowledge is maintained and continuously improved. A core part of your role is to assess the impact of
You will lead Major Global QA Medical Device projects, and you will support the Ferring Manufacturing sites as main point of contact regarding Medical Devices and device constituents of combination/medicinal products. Contribute to QMS improvements