Associate, Quality Control Analytical

Position Summary

AstraZeneca is seeking an energetic and experienced individual with cell therapy quality control background to join our Quality Control (QC) team. The successful candidate will contribute to the advancement of our product pipeline by playing a crucial role in Quality Control Operations including sample management, equipment management and reagent management in the AstraZeneca Quality Control Laboratory. This position is essential for ensuring that the laboratory meets the high standards required for CGMP Quality Control Operations.

This position operates on the following shift, and is subject to change:

• Monday to Friday, 5X8, 9AM-5:30PM
  
  

Responsibilities

• The candidate will be primarily responsible for the receipt, storage, inventory, and distribution and preparation of samples, controls, reagents and standards used in analytical testing, utilizing paper and computer-based inventory systems.
• The candidate will also be responsible for the operation, organization and maintenance of Temperature-Controlled Storage Units and ensure that samples, reagents, standards and controls are stored in appropriate temperature conditions utilizing paper and computer-based asset systems.
• The candidate will support the calibration and maintenance activities required for QC equipment using computerised asset management software
• The candidate will complete and document activities in accordance with CGMPs, SOPs, and protocols.
• Perform compendial assays and processing of samples as needed.
• Report deviation events to QC management.
• This position is essential for ensuring that the laboratory meets the high standards required for CGMP lot release and stability testing
• The role also involves contributing to the writing and revision of Standard Operating Procedures (SOPs) and other CGMP documentation.
• The position requires a strong background in laboratory practices, general testing methodology, assay troubleshooting, and familiarity with Quality Systems.
• Perform other duties as assigned.
• Ability to follow safety procedures outlined in the Safety, Health and Environmental requirements.
  
  

Qualifications

• Associate's degree preferably in Biology or equivalent with 2-3 years of relevant CGMP laboratory experience
• Strong experience with receipt, storage, inventory control, and distribution of samples and reagents for analytical testing.
• 1-2 years executing routine and non-routine analysis for CGMP compendial assays (Appearance, pH, etc.)
• Experience in customer service and strong communication skills.
• Familiar with basic computer applications such as Microsoft Outlook, Word and Excel.
• Experience with labeling and preparation of reagents, controls and reference standards.
• Experience operating and maintaining Temperature-Controlled Storage Units, including cryogenic (LN2) freezers.
• The ideal candidate will possess excellent attention to detail, strong communication skills, and the ability to analyze raw data effectively.
  
  

Preferred Qualifications

• Experience in Cell &/or Gene Therapy
• Bachelor's degree preferably in Biology or equivalent with 1-2 years of relevant CGMP laboratory experience.
  
  

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and daring world.

At AstraZeneca, we follow the science and pioneer new frontiers. Our team is dedicated to Oncology with a vision to eliminate cancer as a cause of death. With multiple indications and high-quality molecules at all stages of our innovative pipeline, we keep pushing forward. We fuse cutting-edge science with the latest technology to achieve breakthroughs. Backed by investment, we aim to deliver six new molecular entities by 2025. Our environment is built on courage, curiosity, and collaboration, empowering you to lead at every level and take smart risks that drive patient outcomes.

Ready to make a difference? Apply now and join us on this exciting journey!

The annual base pay for this position ranges from $55,920.80 - $83,881.20. 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

16-Apr-2026

Closing Date

22-Apr-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.