Senior Specialist, QC

About Allogene Allogene Therapeutics, with headquarters in South San Francisco, is a clinical‑stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of “off‑the‑shell” CAR T cell product candidates with the goal of delivering readily available cell therapy on‑demand, more reliably, and at greater scale to more patients. About the Role Allogene is seeking a Senior Specialist, QC to provide scientific technical expertise to the QC analytical laboratory. You will act as a Subject‑matter Expert (SME) for all cell‑based methods including but not limited to potency, cytotoxicity, flow cytometry, qPCR and ddPCR, and immunoassays. You will be responsible for the review and approval of test records and documentation generated from the QC laboratory and other contract testing laboratories (CTLs) as needed. You will support daily laboratory operations, scheduling, training, and method lifecycle related activities including development, optimization, troubleshooting, transfer, and validation of analytical methods. You will perform routine laboratory testing as needed to ensure all operations are completed within agreed upon turn‑around time (TAT). You will support deviation investigations, CAPA initiation and completion, and method‑related change management as needed. This position reports into the Associate Director, Quality Control and is based out of our Newark, CA location. Responsibilities Serve as a Subject Matter Expert (SME) for QC test methods including flow cytometry, cell‑based assays, ELISA, qPCR and ddPCR and demonstrate ability to design and develop methods as needed. Demonstrate expertise in the operation, maintenance and troubleshooting of instruments; train and qualify junior laboratory members on test methods. Lead method validation and transfer activities, by participating in the design and authoring of validation protocols/reports and support execution of validation and transfer exercises as needed. Define and execute critical reagent qualification programs and help in establishing and maintaining the critical reagents qualification program for all methods as needed. Support the implementation of reference standards and controls programs for analytical methods and monitor analytical methods performance and elevate any issue. Troubleshoot / optimize analytical methods as needed; identify opportunities to improve efficiency. Support Associate Director by assisting in laboratory operations, including scheduling, training and troubleshooting to ensure all operations are in full compliance with applicable SOPs and safety guidelines. Perform QC analytical testing to support the release and stability of final products as needed. Review and approve test records and documentation generated from the QC laboratory and other CTLs, evaluate data, and interpret trends as needed. Ensure laboratory maintenance and cleaning activities are performed in a timely manner. Perform technical investigations of discrepancies, Out Of Specification (OOS), unexpected results and support the implementation of corrective and preventative actions. Assist with addressing questions during GMP audits and support inspection‑related needs as required. Support the team’s responsibilities for the performance of all testing and/or for regulatory requirements pertinent to the QC laboratory. May represent QC at operational and cross‑functional meetings. Other duties as assigned. Position Requirements & Experience Bachelor’s degree in a scientific discipline with at least 8 years of experience performing relevant activities including working in a GMP environment (advanced degree preferred). Broad knowledge and experience performing cell‑based assays, flow cytometry, ELISA, qPCR, and ddPCR. Experience in analytical method development / validation / transfer and reagent qualification and maintenance. Ability to troubleshoot and optimise methods as needed. Experience conducting unexpected / OOS investigations and CAPA initiation. Thorough understanding of regulatory requirements for drug substance and drug product testing. Previous experience in GMP audits and inspection‑related support. Ability to solve problems of moderate to complex level. Proficient in Microsoft Office Suite and Statistical software (JMP). Strong communication and collaboration skills to effectively interact with cross‑functional teams. Excellent organisational skills and an ability to prioritise effectively to deliver results within aggressive timelines with the ability to work independently and as part of a team. Candidates must be authorised to work in the U.S. We offer a chance to work with talented people in a collaborative environment and provide a top‑notch compensation and benefits package, which includes an annual performance bonus, equity, health insurance, generous time off (including 2 annual holiday company‑wide shutdowns) and much more. The expected salary range for this role is $130,000 to $155,000 per year. Actual pay will be determined based on experience, qualifications, geographic location, business needs and other job‑related factors permitted by law. As an equal‑opportunity employer, Allogene is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, colour, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status or other non‑job‑related characteristics or other prohibited grounds specified in applicable federal, state and local laws. We also embrace differences in experience and background, and welcome diversity of opinions and thought, designed to create a stronger and better Allogene that is focused on developing life‑changing products for patients. #J-18808-Ljbffr Allogene Therapeutics