Cell Therapy Specialist I
Listed on 2026-08-09
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Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing & Industrial Operations
Cell Therapy Specialist I
We're here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.
Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows.
We are seeking a highly motivated, Cell Therapy Specialist I to join our newly formed Cell Therapy Manufacturing team at our brand new, state of the art, commercial Cell Therapy facility in Frederick, Maryland. The Cell Therapy Specialist will perform and/or verify all tasks associated with the manufacture of commercial product following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations as well as works as part of a team to execute GMP runs in close collaboration with Materials Management, Quality Control and Quality Assurance.
Responsibilities include, but are not limited to:
- Perform all tasks associated with the manufacture of clinical product following batch records and SOPs
- Work as part of a small team to execute GMP runs in close collaboration with Process Development and Quality
- Assist in the development of standard operating procedures, batch records, deviations and change controls
- Successfully troubleshoot processing and equipment issues
- Other duties as assigned
Basic Qualifications:
- Associate and 1+ years of biomanufacturing experience OR
- High School Diploma/GED and 2+ years of biomanufacturing experience
Preferred Qualifications:
- Bachelor's degree and/or advanced degree or 3 or more years of cGMP experience in a manufacturing pharmaceutical/biotechnology environment
- Cell culture processing experience
- Previous experience with cell therapy products is a plus
- Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing, cell culture products
- Strict adherence to SOPs and cGMP regulations, the ability to accurately complete documentation associated with clinical manufacturing
- Excellent aseptic/sterile techniques and prior experience with cell culture, cell culture equipment including Wave bioreactors
- Experience with handling and propagation of human primary cells, including T cells
- Excellent skill in Microsoft word, Excel and data analysis
- Ability to think critically, and demonstrated troubleshooting and problem solving skills
- Self-motivated and willing to accept temporary responsibilities outside of initial job description
- Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment
- Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities
- Ability to work off-shift and extra hours as required
The salary range for this position is: $60,095.00 - $77,770.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package.
Benefits include company-sponsored medical, dental, vision, and life insurance plans*.
* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
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