Quality Assurance Associate
About this opportunity
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 coordinate 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.
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
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 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.
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 385 comparable Associate Quality roles across 90 biopharma companies.
Salary context
44 of 385 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 385 comparable roles
+ 31 more countries
Seniority mix
385 of 385 peers have a known seniority level
Therapeutic area mix
1 of 385 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.