Quality Assurance Associate
- Location
- California
- Listed
- 6 days ago
About the role
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 exp ecte d to in dependently coordinate and manage timelines for batch record reviews. You will be expected to provide support for both the Santa Mo nica, 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.
- Handle other duties as requested by supervisor/manager to support Quality.
- Administrative Tracking of QA metrics
- On the Floor QA support
Qualifications
- BS in biological sciences or a related field is required.
- 1-2 years of experience withn GMP regulated industry.
- 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.
- Ability to take ownership, initiative, and self-accountability.
- 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
Pay and benefits
The annual base pay (or hourly rate of compensation) for this position ranges from $ 55,920.80 - $83,881.20. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
- Date Posted
- 03-Nov-2026
- Closing Date
- 29-Nov-2026
Equal opportunity and legal notices
Our 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.
From AstraZeneca's careers page, first listed on Rolev.ai on November 4, 2026. Rolev.ai is not the employer.
How Rolev.ai helps with this application
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Common questions
Where is the Quality Assurance Associate job at AstraZeneca located?
This Quality Assurance Associate position at AstraZeneca is located in California. Always check AstraZeneca's application page for specific state eligibility or relocation policies.
How do I apply for the Quality Assurance Associate position at AstraZeneca?
This listing links directly to AstraZeneca's Workday application page. You can apply directly on AstraZeneca's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.