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Quality Assurance Associate

AstraZeneca

US – Santa Monica Colorado Avenue – CA permanent

Posted: March 20, 2026

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Quick Summary

We are seeking a highly motivated individual to join our Quality Assurance team, where you will be responsible for conducting quality reviews, documenting records, and managing timelines for batch record reviews. The ideal candidate will have experience in cell therapy quality assurance and be able to work independently in a fast-paced environment. This is a full-time position with a competitive salary and benefits package.

Job Description

Position Summary: 

AstraZeneca is seeking an energetic and experienced individual with cell therapy quality assurance background to join our Quality Assurance (QA) team. The successful candidate will contribute to the advancement of our product pipeline by performing QA batch record review, label review and verifications, document archival of records, and other assigned tasks. You will also be expected to independently organize and manage timelines for batch record reviews. You will be expected to provide support for both the Santa Monica, CA and Tarzana, CA sites as needed. 

 

Responsibilities include, but are not limited to: 

• Reviews routine manufacturing batch documentation and quality control data for in-process and finished product to support disposition and lot closure. 

• Review routine material release documentation for quality release of raw materials used for manufacturing and quality control testing. 

• Work with Doc Control to ensure archival of batch records. 

• Work with QA doc control to ensure accurate issuance of batch record documentation (i.e. lot/media records and labels) to manufacturing. 

• Provide quality assurance support across technical operations functions (i.e. Manufacturing, Facilities & Engineering, Supply Chain, Quality Control, Analytical Development, Product Development/Manufacturing Sciences & Technology) within AZ to assure compliance with the quality manual and maintain collaborative quality relationships. 

• Perform other duties as requested by supervisor/manager to support Quality. 

• Administrative Tracking of QA metrics 

• On the Floor QA support 

 

Qualifications: 

• BA/BS in Biology, Chemistry, Microbiology, Engineering, or a related field is required (no prior work experience needed). Alternatively, an Associate’s degree with up to 2 years of relevant experience or a High School diploma with up to 4 years of relevant experience is required. Relevant academic laboratory experience, coursework, or internships are a plus.

• Must be able to work on multiple projects simultaneously and demonstrate organizational, prioritization, and time management proficiencies. 

• Flexibility of occasionally working in weekend or holidays to support lot release. 

• Demonstrated ability to take ownership, initiative, and self-accountability. 

• Demonstrated ability to collaborate, work, and communicate effectively across organizational interfaces in a fast-paced dynamic team setting. 

• Attention to detail and quick learning/application of concepts and information. 

• Knowledge of cell culture techniques and proficient in MS Word, Excel, Power Point and other applications. 

• Ability to communicate and work in a self-guided manner with scientific/technical personnel. 

 

​Preferred Qualifications: 

• Experience in Cell or Gene Therapy 

• Well versed in various cell therapy manufacturing processes 

#LI-onsite #CellTherapy

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and daring world.

At AstraZeneca, we follow the science and pioneer new frontiers. Our team is dedicated to Oncology with a vision to eliminate cancer as a cause of death. With multiple indications and high-quality molecules at all stages of our innovative pipeline, we keep pushing forward. We fuse cutting-edge science with the latest technology to achieve breakthroughs. Backed by investment, we aim to deliver six new molecular entities by 2025. Our environment is built on courage, curiosity, and collaboration, empowering you to lead at every level and take smart risks that drive patient outcomes.

Ready to make a difference? Apply now and join us on this exciting journey!

The annual base pay for this position ranges from $65,556.80 - $98,335.20. 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. Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, 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. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

Date Posted

20-Mar-2026

Closing Date

30-Mar-2026Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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