Search the 11 jobs at Neogene Therapeutics

The Associate, Quality Control Analytical will perform analytical testing, support method development, and ensure the QC Analytical laboratory operates effectively. Responsibilities include executing assays for cell therapy products, reviewing technical documents, and collaborating within a dynamic team environment.

The Research Associate in Process Development at AstraZeneca focuses on designing and executing studies to enhance clinical manufacturing processes of engineered T cell therapies, performing experiments such as flow cytometry and cell culture, collaborating on technical discussions, and preparing various reports and procedural documents.

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 Associate Scientist will design and execute experiments to develop and optimize manufacturing processes for engineered T cell therapies, collaborate with cross-functional teams, analyze data, maintain compliance with regulatory requirements, and contribute to technical discussions.

The Associate Scientist will develop TCR-based immunotherapies, perform clinical biospecimen characterization, data analysis, and quality control for clinical samples. Responsibilities include documenting lab procedures, conducting peer audits, collaborating with team members, and analyzing results for presentations or reports.

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 Global Brand Planner at AstraZeneca's Oncology R&D division is responsible for overseeing the end-to-end tactical planning process for cell therapy products, managing brand sales and operations planning, budget management, and collaborating on supply chain change projects to ensure effective execution and alignment with strategic goals.

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 Principal Engineer will develop and implement technology transfer strategies, ensure smooth transitions into GMP manufacturing, and provide technical expertise for process troubleshooting. Responsibilities include technical writing, creating complex datasets, establishing operating ranges, and documenting procedures. The role requires collaboration with partners to meet production needs.

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.