Senior Associate, Cell Therapy Manufacturing

Allogene Therapeutics•Newark, NJ

22h•Onsite

About The Position

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) product candidates 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. About the Role: We are seeking a highly motivated Senior Associate, Cell Therapy Manufacturing to join our team. You will work within the Manufacturing team in supporting our efforts in an exciting area of cancer immunotherapy. 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. The position will report to the Associate Director, Manufacturing and will support the successful tech transfer and operational readiness process, using knowledge of cGMP regulations to ensure manufacturing readiness. This position is based out of Newark, California location.

Requirements

Bachelor’s or associate degree in relevant science or engineering discipline with at least 4 years of experience in cGMP biologics or cell therapy manufacturing
Experience with aseptic processing in Grade A biosafety cabinets and Grade B clean rooms and 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
Frequent use of a computer monitor, keyboard and mouse and personal protective equipment
Physical requirements of the role include lifting, carrying, pushing or pulling up to 30 pounds, frequent periods of sitting, walking, and standing, occasional climbing stairs or ladders, bending or stooping, crouching or squatting, occasional fine finger dexterity/ including grasping or pinching and color, vision, and depth perception required for inspection or test related jobs
Occasional work in cold rooms and freezers and use of hazardous materials and chemicals required
Excellent organizational skills and an ability to prioritize effectively to deliver results within reasonably established timelines
Ability to work independently and as part of a team
Strong interpersonal skills including verbal and written communication are essential in this collaborative work environment
Candidates must be authorized to work in the U.S.

Nice To Haves

Cell culture processing experience in handling and propagation of human primary cells strongly preferred

Responsibilities

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