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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 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
Responsible for leading and coordinating microbiology laboratory operations, with primary focus on microbiological investigations, microbial method validation/verification, qualification of new laboratory equipment, contamination control
You will serve as the global technical authority for our CMVD Single-Pill Combination (SPC) portfolio. You will lead a team of Subject Matter Experts (SMEs) to ensure the seamless commercialization, scale-up, and lifecycle management of complex OSD