Analyst Ii, Qc Cell And Molecular Biology

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-shelf" 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. For more information, please visit www.allogene.com, and follow @AllogeneTx on X (formerly Twitter) and LinkedIn.

About the role:

Allogene is seeking an Analyst II, QC Cell and Molecular Biology to support routine testing and logistical activities in the QC laboratory. Working in a GMP environment, you will execute compendial test methods (pH, Volume, appearance, Osmolality) and core laboratory testing from ELISA, Cell Culture/counting, Flow cytometry, PCR, and other related testing. The Analyst will also support logistical activities in the lab including sample receipt and will support GMP QC laboratory maintenance by managing and/or monitoring facilities, and laboratory equipment and reagents. This position is based out of our Newark, CA location.

We encourage applicants who believe they have the skills and drive to succeed at Allogene to apply for this role.

Responsibilities include, but are not limited to:

• Performs QC analytical testing to support the release and stability of final products to support the release of products for commercial use, with consideration of compliance, quality, and consistency.
• Review test methods data and supporting documentation.
• Maintains GMP laboratories by monitoring lab equipment, pipettes, etc. and availability of lab supply. Perform instrument calibration and equipment cleaning as needed.
• Support minor equipment troubleshooting, laboratory maintenance, and cleaning activities.
• Manages GMP and non-GMP samples, order and receive lab reagents and materials, and manages the inventories. Support ordering and qualification of critical reagents as requested.
• Accurately follows relevant SOPs, performs all activities in accordance with cGMP requirements reports abnormalities.
• Documents test results to ensure completeness and accuracy per cGMP. Keeps accurate documentation and tracks record.
• Support troubleshooting with minor assay performance issues and support the SOP related activities as requested.
• Supports Discrepancy Management investigations and implementation of corrective and preventative actions as instructed.
• Contributes toward the development and revision of SOPs and Test Methods.
• Support method validation and transfer of QC CMB methods and critical reagent qualification by executing as instructed.
• Support Change Control by gathering and providing information necessary to support simple changes to existing methods.
• Perform non-routine laboratory tasks.
• Other duties as assigned.

Position Requirements & Experience:

• B.S. degree in a scientific discipline with 3+ years of experiences in a cGMP compliant environment or equivalent combination of education and experience.
• Demonstrated knowledge of laboratory techniques such as Flow cytometry, ELISA, Cell culture and Cell-based assay, PCR etc.
• Must have previous working experience in aseptic technique.
• Experience in maintenance of GMP laboratory, laboratory equipment, and the status of pipettes and supplies. Able to perform QC laboratory maintenance related duties as assigned
• Able to follow instructions and SOPs precisely and able to make/keep accurate and contemporaneous documentation.
• Experience of supporting analytical method validation and transfer and reagent qualification.
• Experience of supporting troubleshooting and optimization of the method to improve the performance.
• Experience of supporting Invalid, OOE, and OOS investigation and CAPA initiation.
• Able to solve minor problems and troubleshoot, as necessary.
• Good organizational and planning skills, and an ability to work efficiently.
• Able to learn new skills rapidly and achieve proficiency.
• Able to seek and accept input from more senior team members for the performance of assignments as needed.
• Able to multi-task and adapt to changing business requirements in a dynamic corporate environment.
• Good communication skills. Able to maintain good interaction with peers and leadership within Quality Control
• Physically able to lift LN2 freezer rack or move up to 20L buffer if needed as laboratory activities.
• Candidates must be authorized 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 $40.00 to $45.00 per hour. 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, color, 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 with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients.

#LI-EL1