Associate Specialist, Cell Therapy
We are looking for an Associate Specialist, Cell Therapy to support our dynamic Manufacturing team in the production of TCR-T, CAR-T, and allogeneic cell therapy investigational products. This role is based in Tarzana, CA, with occasional travel to Santa Monica, CA. You will report to the Associate Director of Manufacturing, NGF70 or Manufacturing Manager, NGF70.
The Associate Specialist, Cell Therapy role will ensure successful manufacture and release of cell therapy products by following established processes in full compliance with cGMP. You will support manufacturing operational readiness and the successful technology transfer of pipeline products using knowledge of cGMP regulations.
You Will:
• Support GMP readiness activities to support clinical manufacturing, including equipment setup, basic qualification support, and facility prep under the guidance of senior staff.
• Follow established procedures and protocols to ensure compliance with safety standards, quality systems, and cGMP requirements.
• Support the drafting and revision of Standard Operating Procedures (SOPs) and documentation required for manufacturing processes.
• Aid in the preparation of manufacturing areas and routine maintenance of equipment, including setup of automated and manual systems.
• Follow proper gowning and cleaning procedures within the manufacturing environment.
• Monitor and restock material and supply inventories in cleanroom areas to ensure readiness for production activities.
• Assist with staging and verification of materials and equipment before manufacturing activities.
• Collaborate with Manufacturing and Process Development teams to support execution of process steps and ensure seamless tech transfer activities.
• Maintain detailed records and documentation by cGMP standards.
• Communicate effectively with leads and team members and escalate issues or deviations.
• Participate in team meetings and contribute to continuous improvement projects.
• Perform other assigned responsibilities to support daily manufacturing operations and project goals.
You Have:
• Minimum of two (2) years of experience in a GMP or laboratory setting with a High School diploma, or equivalent combination of education and experience.
• Associate or bachelor's degree in a science or engineering discipline is preferred.
• Basic understanding of CGMP regulations and aseptic techniques.
• Familiarity with cleanroom procedures, equipment setup, and documentation practices in a regulated environment is a plus.
Additional Requirements
• Familiarity with industry practices; cell therapy manufacturing experience is a plus but not required.
• Ability to follow instructions and established protocols with attention to detail.
• Use sound judgement to identify and escalate issues or deviations to senior team members.
• Help achieve team goals through collaboration and reliable task execution.
• Prioritize assigned tasks and manage time effectively to support team schedules.
• Work is closely reviewed to ensure accuracy and alignment with established procedures.
The annual base salary for this position ranges from $62,000 to $93,000. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles).
Our Benefits:
Benefits offered include:
A qualified retirement program [401(k) plan]
Paid vacation, holidays, and paid leaves
Health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment.
#celltherapy #LI-Onsite
Date Posted
14-Jul-2025Closing Date
30-Jul-2025Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.