Associate Specialist, Cell Therapy

AstraZeneca•Los Angeles, CA

1d•$65,082 - $97,622

About The Position

This role involves conducting technical tasks to support manufacturing and packaging operations, adhering to standard operating procedures (SOPs) and safety requirements. The Associate Specialist will assist with diagnostic tasks, participate in maintenance activities under supervision, and build foundational knowledge of manufacturing systems. They will contribute to continuous improvement by providing feedback and collaborate with team members to support digital adoption. The position requires an eagerness to learn and adapt to new digital tools and technologies.

Requirements

High School Diploma with at least 5 years of relevant GMP manufacturing experience, or Bachelor’s degree with at least 2 years of relevant experience in a science, engineering, or related field
Understanding of cGMP processes and regulated manufacturing requirements
Knowledge of aseptic technique, cleanroom behavior, and GMP documentation practices
Experience supporting GMP clinical manufacturing, technology transfer, or process implementation
Ability to develop solutions to routine and moderately complicated problems using established procedures, precedent, and good judgment
Ability to plan and coordinate assigned work with limited supervision
Strong written and verbal communication skills
Ability to work effectively in a fast paced and changing manufacturing environment

Nice To Haves

Cell therapy manufacturing experience
Experience with primary human cell culture, single use technologies, or automated cell processing equipment
Experience with paper and electronic batch records, manufacturing execution systems, inventory systems, or quality management systems.

Responsibilities

Conduct technical tasks such as basic equipment checks, make vital adjustments, and perform operational duties to support smooth manufacturing or packaging operations.
Follow defined standard operating procedures (SOPs), adhere to safety requirements, and maintain accurate documentation to ensure compliance.
Assist with routine diagnostic tasks or identify simple faults, advancing more complex problems to experienced team members for resolution.
Participate in activities like cleaning, calibration, test setup, or performing repairs under supervision to maintain operational efficiency.
Build foundational knowledge about manufacturing systems, tools, and production workflows to help maintain consistent output and high-quality standards.
Contribute to continuous improvement efforts by providing detailed and insightful feedback based on daily operational experiences.
Is eager to build skills in, quickly adapt to, and embrace new digital tools and technologies.
Collaborate with team members to support digital adoption within area.