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Associate, Cell Therapy Manufacturing (Multiple Positions)

Manufacturing | Newark, CA | Full Time

Job Description

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™) therapies for cancer. Led by a world-class management team with significant experience in cell therapy, Allogene is developing a pipeline of “off-the-shelf” CAR T cell therapy 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 Twitter and LinkedIn.

We are seeking multiple highly motivated Cell Therapy Associates across all experienced levels to join our Manufacturing team. They will work within the Manufacturing team in supporting our efforts in an exciting new area of cancer immunotherapy. This position is based out of Newark, CA.

The position will support the successful tech transfer and operational readiness process, using knowledge of cGMP regulations to ensure manufacturing readiness. Responsibilities of primary importance are: to ensure the successful, time-sensitive GMP manufacture and release of cell therapy products; to follow all processes and procedures related to operations in full compliance with cGMP, CFRs, site quality systems and company policies; and to promote a culture of quality and compliance.


The successful candidate will have experience in a regulated biotech or pharmaceutical setting and will have proven competency and expertise in the GMP manufacture of cell-based therapies.

Responsibilities include, but are not limited to:

  • Perform process unit and support operations described in standard operating procedures (SOPs) and batch records including: PBMC, media and solution preparation; CAR-T cell drug substance preparation; and CAR-T drug product fill operations
  • Accurate and timely completion of documentation required by protocols, SOPs, and batch records
  • Maintain aseptic technique during processing of products to ensure the integrity, viability and sterility of cell therapy products from PBMC thaw to final formulated drug product cryopreservation
  • Perform tasks in a manner consistent with safety policies, quality systems, and cGMP requirements
  • Timely completion of training assignments to ensure the necessary technical skills and knowledge are applied compliantly during GMP operations
  • Assist in setting up manufacturing areas and equipment, including complex automated cell processing, cell expansion and filling equipment
  • Update and revise manufacturing operating procedures that are technically sound, promote effective and efficient operations, and comply with cGMP requirements·       
  • Routinely monitor, clean, prepare and operate processing and analytical equipment in Grade B/C areas
  • Follow all cleaning and gowning procedures for the facility
  • Perform error free calculations of media component and cell concentration, dilution, viability during production
  • Must maintain and apply knowledge regarding donor information, screening and testing, labeling and product acceptability and release criteria
  • Be flexible and adaptable to schedule and procedural changes to ensure timely preparation of products with highest quality
  • Maintain current inventory of supplies kept in specified kitting and staging areas and CAR-T suites
  • Other duties as assigned

 

Position Requirements & Experience:

  • Bachelors or Associates in relevant science or engineering discipline with 1-3 years of experience in cGMP biologics or cell therapy manufacturing; or
  • 3+ years in cGMP manufacturing biologics or cell therapy manufacturing
  • Aseptic processing in Grade A biosafety cabinets and Grade B clean rooms
  • Cell culture processing experience in handling and propagation of human primary cells strongly preferred
  • Universal precautions for handling human derived materials in BSL-2 containment areas
  • Knowledge of cGMP regulations and FDA guidance applicable to biologics and/or cell therapy
  • Excellent interpersonal, oral and written communication skills
  • Strong technical writing ability strongly preferred
  • Ability to work off-shift and long hours as required
  • Frequent use of a computer monitor, keyboard and mouse required
  • Frequent lifting, carrying, pushing or pulling up to 30 pounds required
  • Frequent periods of sitting, walking, and standing required
  • Frequent use of personal protective equipment required
  • Occasional climbing stairs or ladders, bending or stooping, crouching or squatting required
  • Occasional fine finger dexterity/ including grasping or pinching required
  • Occasional use of hazardous materials and chemicals required
  • Occasional work in cold rooms and freezers required
  • Color, vision, and depth perception required for inspection or test related jobs.
  • Candidates must be authorized to work in the U.S.


As an equal opportunity employer, Allogene Inc. 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. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact the careers email at www.allogene.com for assistance.

 

For more information about equal employment opportunity protections, please view the ‘EEO is the Law’ poster.



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