Cell Therapy Specialist I
Kite PharmaAbout the role
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.
Job Description
We are seeking a highly motivated Cell Therapy Specialist I to join our Cell Therapy Manufacturing team at a state-of-the-art commercial cell therapy facility in Frederick, Maryland. This role is responsible for performing and verifying tasks associated with the manufacture of commercial and clinical cell therapy products in accordance with batch records and standard operating procedures. The Cell Therapy Specialist I works as part of a cross-functional team to execute GMP manufacturing runs in close collaboration with Materials Management, Quality Control, and Quality Assurance.
Key Responsibilities
Perform and verify manufacturing activities for commercial and clinical cell therapy products in compliance with approved batch records and SOPs
Troubleshoot processing and equipment issues and communicate findings to management in a timely manner
Operate, monitor, clean, and prepare automated cell processing equipment in Grade B and C cleanroom environments
Maintain strict adherence to cGMP requirements, safety standards, and gowning and PPE requirements for classified manufacturing areas
Complete all required training assignments to maintain technical proficiency and regulatory compliance
Identify opportunities to improve manufacturing efficiency and compliance
Support investigations, deviations, and change control activities as needed
Wear a respirator when working with hazardous disinfectants, as required
Basic Qualifications
Associate degree with a minimum of 1 year of relevant experience, or
High School Diploma or GED with a minimum of 2 years of relevant experience
Preferred Qualifications
Bachelor’s Degree
Prior experience working in a GMP-regulated manufacturing environment or aseptic processing environment
Experience supporting investigations, deviations, and change control processes
Physical and Work Environment Requirements
Availability to work holidays based on operational requirements .
Ability to work in a cleanroom manufacturing environment
Ability to wear required PPE, including respirators, for extended periods
Ability to perform tasks that may require standing, lifting, and repetitive motions
For additional benefits information, visit:
https://www.gilead.com/careers/compensation-benefits-and-wellbeing
* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds. Free account required — sign up in 30s
Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit Apply for this role