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The Scientist will support the development of cell and gene therapies, focusing on mammalian cell culture, T cell preparation, retroviral vector design, and various assays and molecular biology techniques. You will work independently and collaboratively in a fast-paced environment, utilizing skills in flow cytometry and cell manipulation, among others, to drive innovation in bispecifics.

The Staff CMC Regulatory Sciences Specialist oversees CMC aspects of global submissions, focusing on regulatory strategies and the preparation of submissions for non-US/EU markets. The role involves developing processes, managing cross-functional teams, providing regulatory guidance, and monitoring trends in non-US/EU markets.

The Process Development Associate II in Purification Development is responsible for developing purification processes, documenting experiments, maintaining laboratory instruments, and supporting technology transfers. You will also engage with team members to improve efficiency and safety, present findings in meetings, and assist in training peers and interns.