Search the 7 jobs at Neogene Therapeutics

The Senior Scientist in Translational Sciences analyzes clinical biospecimen data focusing on flow cytometry and supports data quality for clinical samples. Responsibilities include developing insights, performing peer audits, collaborating with team members, and preparing documentation. This role requires a strong background in immunology and data analysis.

The Research Associate will conduct routine testing and operational tasks in Analytical Science including cell culture, flow cytometry, and immunoassays to support T cell therapy processes. Responsibilities include improving test methods, maintaining equipment, and collaborating with other teams to ensure accurate laboratory operations.

The Principal Associate in Quality Control Analytical will perform QC analytical method qualifications, conduct sample analyses, and ensure laboratory operations align with standards. They will handle various analytical assays and support method developments while preparing and reviewing technical documents and SOPs.

The Manager, Quality Control Analytical will oversee sample and reagent management in the QC Analytical laboratory, ensuring compliance with GMP and coordinating with Supply Chain. Responsibilities include resource planning, mentoring team members, drafting SOPs, performing stability testing, and managing laboratory investigations. The role involves ensuring efficient lab operations and maintaining communication with stakeholders.

The Senior Scientist will lead bioassay development, manage a lab team, and optimize analytical methods for cellular therapy products, ensuring compliance with regulatory standards. Responsibilities include developing and implementing cell-based assays, writing technical reports, and collaborating with various teams for product characterization and testing.

The Senior Scientist in Process Development leads the development of manufacturing processes for autologous T-cell therapies, ensuring application of best practices and technologies. Responsibilities include overseeing technology transfer, collaborating on clinical activities, performing data analysis, designing scalable manufacturing processes, mentoring staff, and reporting progress to management.

The Manager, QA Operations is responsible for ensuring compliance with quality systems and assessing regulatory risks. This role involves providing quality assurance support across departments, conducting audits, managing deviations and CAPAs, overseeing production documentation, and developing QA procedures. The manager also participates in internal reviews and supports regulatory inspections and new product introductions.