Search the 12 jobs at Neogene Therapeutics

The Senior Process Engineer is responsible for supporting the development of a clinical manufacturing process of engineered T cells with patient-derived neo-antigen specific TCRs. This role involves designing, executing, and analyzing process development studies, collaborating with the team, and contributing to manufacturing support efforts in a cGMP environment.

The Specialist, Quality ensures compliance with quality system's procedures and assessing regulatory and quality risks in activities and processes according to regulatory agency guidelines and company practices. Responsibilities include providing quality assurance support across technical operations functions, leading deviations and investigations, managing change controls, providing trainings, and reviewing manufacturing documentation.

As a Global Brand Planner for Cell Therapy at AstraZeneca, you will drive strategic planning and execution of innovative cell therapy products across the global supply chain. Responsibilities include tactical planning, brand S&OP, supply chain configuration, budget management, and collaboration in supply chain change projects.

Looking for an experienced Principal Engineer of MSAT to lead technology transfer processes in manufacturing. Must have expertise in technical writing, regulatory guidelines, and GMP environments. Salary range is $160,000 to $201,000 per year in Santa Monica, CA.

Join Neogene's Translational Sciences group as a Data Scientist to lead bioinformatic research efforts from multi-omic clinical trial data. Customize tools, design methodologies, define workflows, collaborate on projects, and communicate findings.

Seeking a highly motivated Senior Scientist with expertise in immuno-oncology to join the Analytical Development team. Responsible for developing analytical assays for characterizing T-cell therapy drug substance and product. Must have a PhD in Immunology or related discipline and 2+ years of experience.

Looking for a motivated Senior Research Associate with experience in immunology, cell biology, and process development to join the PD team. Responsibilities include implementing process development studies, performing cell culture of T cells, and collaborating within the project team. MS degree in relevant field with 1+ years of industry experience or BS degree with 2+ years of industry experience required.

Looking for a Principal Research Associate with 4+ years of experience in Pharmaceutical or Biotechnology industry to join the Quality Control team. Responsibilities include performing analytical assays, method qualification, and supporting routine activities. BS or MS in biological sciences required. Base salary ranges from $85,000 to $100,000 yearly.

Seeking an experienced individual with a background in cell therapy quality control to join the Quality Control team. Responsibilities include performing analytical assays, supporting method development and qualification, preparing technical documents, and collaborating effectively across teams.

The Manager, QA Operations ensures compliance with quality system procedures, assesses regulatory and quality risks, and supports multiple departments within Neogene. Responsibilities include batch documentation, approval of deviations and CAPAs, new product introductions, quality assessments, regulatory inspections, and more.

The Senior Scientist, Process Development leads process development activities for cell therapy products, collaborates with various departments, and oversees the implementation of manufacturing processes. Responsibilities also include data analysis, study interpretation, and preparation of reports and SOPs. The role requires a PhD in related fields with 3+ years of experience or MS with 6+ years of industry experience.

The Administrative Assistant at AstraZeneca's Oncology R&D division provides administrative support to the Vice President, Manufacturing. Responsibilities include calendar management, travel arrangements, meeting coordination, event planning, and creating professional documents. The role requires 10-12 years of administrative assistant experience with biotech or pharmaceutical experience, and proficiency in Microsoft Excel and Adobe PDF.