New · posted Oct 28
AstraZeneca · Biotechnology
Quality Control Specialist
- Tarzana, CA
- On-site
- Full-time
- Associate & Specialist
The role
Introduction to role
Are you driven to ensure cell therapy products meet the highest standards and reach patients without delay? Do you see yourself using rigorous analytical science to accelerate safe, effective treatments to those who need them most? Join our Quality Control team and take on a high-visibility role where your decisions and data will directly influence product release and stability strategies.
In this role, you will be a key contributor to advancing our cell therapy pipeline, owning analytical method qualification and executing critical testing that underpins lot release and in-process control. You will organize, analyze, and present results with clarity, ensuring the QC Analytical laboratory runs reliably and compliantly. Your expertise will be recognized across teams, and your voice will help shape how we deliver consistently high-quality outcomes for patients.
Here, scientific rigor meets real-world impact. You will work alongside specialists who bring diverse perspectives into the same room to unleash bold thinking, applying advanced analytics and modern lab technologies to decisions that put patients first. Your contributions are visible and valued, with opportunities to stretch your skills across functions, learn from peers, and take on meaningful responsibility. We value kindness alongside ambition, support curiosity, and recognize progress—even when it comes through constructive challenge—so you can grow while making a measurable difference in the lives of patients worldwide.
If you are ready to turn your analytical expertise into outcomes that release therapies faster and safer, step into this role and help shape the future of cell therapy quality today.
The annual base pay for this position ranges from $80,910 to $121,364. 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.
What you need
Accountabilities
- Release and Stability Testing: Perform flow cytometry, ELISA, cellular cytotoxicity, dPCR, and cell-based potency assays to enable timely release testing and stability monitoring of cell therapy products and in-process samples, ensuring data integrity and fit-for-purpose results.
- Analytical Method Lifecycle: Support analytical method development, qualification, and technical transfer from Analytical Development; design, execute, and document qualification activities to ensure robust, reproducible methods ready for routine use.
- Technical Leadership and SME Support: Serve as a subject matter expert in technical discussions, document reviews, and investigations; provide data-driven guidance that resolves issues quickly and prevents recurrence.
- Documentation and Compliance: Author and/or review analytical test results, analytical study data summaries and reports, analytical method qualification protocols and reports, and standard operating procedures, ensuring alignment with regulatory expectations and internal quality standards.
- Routine Operations Excellence: Support daily QC analytical activities, monitor lab performance, and ensure the laboratory operates as expected, including occasional off-hour or weekend technical support to meet lot release timelines.
- Mentoring and Knowledge Sharing: Mentor and train associate specialists, elevating team capability and building consistent analytical practice across the laboratory.
- Continuous Improvement and Broader Impact: Identify opportunities to streamline workflows, improve assay performance, and reduce cycle time; translate scientific insights into operational gains that enhance product quality and speed to patients.
Essential Skills/Experience
- Associate’s degree in biological sciences or related field with 4+ years of experience, Bachelor’s degree in biological sciences or related field with 2+ years of experience, or MS in biological sciences or related field with 0+ years of experience is required.
- Flexibility of occasionally working on weekends or holidays to support lot release testing.
- 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.
- Well-versed in various analytical techniques Flow cytometry, qPCR, dPCR, cell-based potency and/or ELISA experience.
Desirable Skills/Experience
- 2+ years of relevant experience in the Pharmaceutical or Biotechnology industry.
- Experience in Cell or Gene Therapy.
- Well-versed in various analytical techniques such as Flow cytometry, qPCR, dPCR, cell-based potency and/or ELISA experience.
Pay and benefits
$80,910 – $121,364 a year
Employer providedQualified retirement programs
Paid time off
Health coverage
Dental coverage
Vision coverage
Short-term incentive bonuses
Where you'll work
Tarzana, CAOn-siteOpen in Maps (opens in a new tab)
More jobs in Tarzana, CA
From the posting
About AstraZeneca
Date Posted
27-Oct-2026
Closing Date
02-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 intelligence
The context around this role
Live data · October 28, 2026
Salary intelligence
How the pay compares
This role's midpoint is 65% above the US median for Quality Control roles at this level.
This roleEmployer provided
Associate & Specialist roles in California10 roles publishing pay
Associate & Specialist roles in the US130 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $80,910 | — | $121,364 |
| California (middle half) | $56,625 | $75,500 | $97,000 |
| All US (middle half) | $49,125 | $61,250 | $78,500 |
This role: AstraZeneca's own published range. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 28, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 341 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not AstraZeneca's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 23 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods12
- Collaboration and leadership6
- Documentation and SOPs3
- Validation and qualification3
- Data and digital systems2
- GMP and compliance1
- Investigations and CAPA1
- Quality systems and risk1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
AstraZeneca on Regulatory Jobs
- 22
- Open roles
- 18
- Distinct roles
- 9
- Locations
By discipline
- Quality15 68%
- Regulatory7 32%
By level
- Associate & Specialist9 41%
- Director7 32%
- Senior & Principal4 18%
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Quality Control Specialist at AstraZeneca
Applications close November 3. $81K–$121K a year, employer provided.