Quality Control Specialist

AstraZeneca plc; Los Angeles (CA); Presencial; USD 81.000 - 121.000; Jornada completa

Descripción de la vacante

AstraZeneca plc is seeking a Quality Control Specialist in Los Angeles, CA. The role focuses on ensuring cell therapy products meet quality standards, impacting release and stability strategies.

You will perform key assays, support method development, and mentor staff while driving continuous improvement in a fast-paced QC lab environment.

Formación

• Associate’s degree in biological sciences with 4+ years of experience, or Bachelor’s with 2+ years, or MS with 0+ years in biology.

Responsabilidades

• Release and stability testing using flow cytometry, ELISA, cellular cytotoxicity, dPCR, and cell-based potency assays.

Conocimientos

Attention to detail

Ownership & accountability

Cross-functional collaboration

Quick learner

Weekend availability

Educación

Associate's degree in biological sciences

Bachelor's degree in biological sciences

MS in biological sciences

Herramientas

Flow cytometry

qPCR

dPCR

ELISA

Descripción del empleo

Quality Control Specialist

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.

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.

Why AstraZeneca

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.

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.