Quality Assurance Associate at AstraZeneca

Los Angeles, California, United States -

Full Time

Start Date

Immediate

Expiry Date

13 Feb, 26

Salary

94980.0

Posted On

15 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, Batch Record Review, Label Review, Document Archival, Cell Culture Techniques, MS Word, Excel, Power Point, Organizational Skills, Time Management, Collaboration, Attention to Detail, Initiative, Self-Accountability, Communication, Technical Support

Industry

Pharmaceutical Manufacturing

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: BS in biological sciences or a related field is required. 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 The annual base pay for this position ranges from $63,320.00 - $94,980.00. 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 14-Nov-2025 Closing Date 27-Nov-2025 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.

Responsibilities

The Quality Assurance Associate will perform QA batch record review, label review, and document archival to support product pipeline advancement. They will also manage timelines for batch record reviews and provide QA support across various technical operations functions.