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Driving all aspects of purification process development, characterization, and technology transfer to cGMP manufacturing for hybrid and continuous processes; Serving as an internal technical resource for cGMP manufacturing and Process Design as well as a
You will provide technical expertise and operational support for cleaning validation activities across pharmaceutical manufacturing processes. Your role ensures that equipment cleaning procedures are scientifically justified, compliant with global
You will be responsible for leading cross-functional regulatory CMC activities to ensure timely preparation and delivery of high-quality regulatory submissions that support product development, registration, and lifecycle management. This position
Your mission is to ensure the smooth execution of strategically aligned research projects, drive scientific and technical excellence across the group, and support the continuous development of the Group Science & Technology. You will act as a key