Cancer Cell Therapy – Process Development Associate - Onsite
FTE: 100%
The Stanford Center for Cancer Cell Therapy (CCT) is seeking a Process Development Associate (PD1) to perform process development consistent with principles of current Good Manufacturing Practice (cGMP) and aligned with the clinical trial investigational phase for treating patients with incurable diseases.
This recruitment is for up to two (2) full time positions.
DESIRED QUALIFICATIONS:
- Experience with CAR T, TCR, T cells, gene editing, and cell therapy process development/manufacturing desired
- Aseptic technique experience and cell culture preferred
- cGMP experience is preferred
Knowledge and following SOPs and batch records preferred
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PHYSICAL REQUIREMENTS*:
- Frequently sit, grasp lightly, use fine hand manipulation, repetitive pipetting, perform desk-based computer tasks, and lift, carry, push, and pull objects up to 15 pounds.
*- Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.
WORKING CONDITIONS:
- May require working in close proximity to blood borne pathogens.
- Position may at times require the employee to work with or be in areas where hazardous materials and/or infectious diseases are present.
- Position may require working in a cGMP clean room environment.
- Position may work with viruses: lentiviruses, adeno-associated viruses, and/or retroviruses.
- Position may work with cancer cell lines or human embryonic stem cells (hESCs).
- Employee must perform tasks that require the use of personal protective equipment, such as safety glasses and shoes, protective clothing and gloves, and possibly a respirator.
- May be exposed to high voltage electricity, radiation or electromagnetic fields, lasers, noise > 80dB TWA, Allergens/Biohazards/ Chemicals, and confined spaces.
May require extended or unusual work hours and business needs.
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WORK STANDARDS:
- Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
- Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors bases on training and lessons learned.
- Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University’s Administrative Guide, http://adminguide.stanford.edu .
Core Duties :
Plan, prepare for and perform human clinical materials biomanufacturing campaigns typically as a verifier. Prepare final formulated cellular products for clinical trials within production timelines and manufacturing schedules.
Plan and perform components of process development and technology transfer for manufacturing of clinical materials, scale-up/scale-out and optimization activities in transitioning and translating pre-clinical, benchtop research into phase appropriate clinical trials.
Perform upstream and downstream components of assigned cGMP project(s)
Identify, document and report operating excursions and facility deficiencies; make recommendations for process improvements and documentation improvements including Standard Operating Procedures (SOP) and manufacturing Batch Records (BR).
Contribute to detailed manufacturing budget; including sourcing, identifying and ensuring qualified and verified raw materials for manufacturing; outlining overall and per/patient costs for project materials and supplies.
Devise and revise methods and/or processes for SOP and Manufacturing Batch Records.
Independently track, verify and ensure cGMP grade raw materials for biomanufacturing. Identify and plan for supply chain and raw materials lead times for scheduled campaigns.
May prepare and submit abstracts or papers for publication in peer-reviewed journals and/or presentation at scientific conferences. Present results during internal meetings.
Minimum Education and Experience
Bachelor's degree in related scientific field or an equivalent combination of education and experience.
Knowledge, Skills and Abilities :
Strong understanding of biological scientific principles
Working experience with aseptic cell culture
Strong computer skills and ability to learn quickly and master computer programs, databases and scientific applications
Ability to work under deadlines with minimal supervision
Ability to maintain relationships and communicate effectively
Excellent organizational skills and demonstrated ability to complete detailed work.
Maintain knowledge of cGMP environment requirements.
