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Your main tasks will include the development and adaptation of single use accessories for the CliniMACS Prodigy and CliniMACS Plus systems. As the group leader, you will take on both technical and disciplinary leadership responsibilities for a dedicated
Laboratory testing of household chemical products and raw materials, in a regulated environment where GMP/GLP standards apply. Formulation of laboratory samples for stability and consumer testing. Participation in industrial trials, supervising compliance
Responsible for providing Regulatory CMC expertise into the development and implementation of the global regulatory strategy, operations and planning for the CMC aspects of assigned projects/products. Responsible for preparing and managing CMC regulatory
Lead, plan, and coordinate daily cell and tissue culture activities in compliance with GMP standards. Supervise and mentor a team of (Senior) Biotech Associates, ensuring quality and efficiency in manufacturing. Initiate and follow up on deviations,
In this role, you’ll provide global scientific and technical leadership, contribute to innovation strategies, and act as a thought leader - both within Lonza and the wider biopharmaceutical industry. Guide development of mammalian USP/DSP processes for