QC Associate – Global Cell Therapy Raw Materials
AstraZeneca is hiring a QC Associate – Global Cell Therapy Raw Materials. It pays $56k-$84k a year and Level rates it ; you can apply on AstraZeneca.
Level's read on this job
- On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
- Tools and skills the posting cites include Ftir, Raman and Hplc.
- Level classifies it as a mid-level role.
- Level lists 1,200+ other open roles at AstraZeneca.
- The role was posted within the past week.
AI in this role
Perform GMP analytical testing of raw materials used in cell therapy manufacturing and maintain QC laboratory operations.
QC Associate – Global Cell Therapy Raw Materials
Position Summary
The QC Associate performs GMP analytical testing of raw materials used in Cell Therapy manufacturing and supports the day-to-day readiness and operation of the QC laboratory. The role follows approved methods and procedures, completes accurate documentation, and supports timely testing of materials in accordance with applicable quality, regulatory, site, and global requirements.
Testing may include chemical and physical analyses, compendial methods, immunoassays, and cell-based assays, as applicable.
Key Responsibilities
Raw-Material Testing and Analysis
- Perform routine and non-routine raw-material testing using approved methods, SOPs, specifications, and protocols for material release or disposition.
- Complete testing accurately and within agreed timelines to support manufacturing requirements.
- Support raw-material qualification and testing activities, as needed.
- Review results and promptly escalate atypical findings, deviations, equipment issues, and data-integrity concerns.
Laboratory and Equipment Upkeep
- Maintain a safe, clean, orderly, and inspection-ready QC laboratory.
- Support the management of laboratory equipment, reagents, standards, consumables, inventory, and waste.
- Perform routine equipment checks and support calibration, maintenance, qualification, and service activities.
Documentation
- Complete accurate, timely, and traceable GMP documentation in accordance with good documentation practices and data-integrity requirements.
- Support the preparation and review of applicable laboratory documents, including SOPs, work instructions, methods, protocols, and reports.
Others
- Support assigned method transfer, qualification, validation, deviation, investigation, and change-control activities.
- Participate in appropriate continuous improvement activities that enhance laboratory efficiency, compliance, and right-first-time execution.
- Work collaboratively cross functionally across the Cell Therapy network
Education and Experience
A bachelor’s or master’s degree, or equivalent, in biological sciences, chemistry, biochemistry, or a related field is required.
- Associate level: B.S. with 2+ years of relevant experience, or M.S. with 0+ years of relevant experience
Required Skills
- Experience with, or exposure to, analytical techniques appropriate to the laboratory, which may include pH, FTIR/Raman, HPLC, ELISA, wet chemistry, and cell-based assays.
- Working knowledge of cGMP, good documentation practices, data integrity, and laboratory safety.
- Awareness of applicable compendial requirements, including USP and EP.
- Ability to follow written procedures and complete work accurately and on time.
- Strong attention to detail, documentation, problem-solving, and communication skills.
- Ability to recognize and escalate testing, equipment, documentation, or procedural issues.
- Ability to work effectively in a collaborative, cross-functional team environment.
Preferred Skills
- Experience supporting raw-material testing or other GMP laboratory activities.
- Experience working with short turnaround times while maintaining quality and compliance.
- Experience with digital laboratory systems, such as electronic laboratory notebooks, LIMS, or SAP.
- Familiarity with Cell Therapy, biologics, or advanced therapy manufacturing environments.
The annual base pay (or hourly rate of compensation) for this position ranges from $55,920.80 to $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
22-Oct-2026Closing Date
22-Nov-2026Our 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.
How we rate this
QC Associate – Global Cell Therapy Raw Materials at AstraZeneca rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.
Prepare for this job
Built from this posting and from similar jobs on Level.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where gmp analytical testing was part of your work. What did you do?
- Tell me about a project where raw material testing was part of your work. What did you do?
- Tell me about a project where cell therapy was part of your work. What did you do?
- Tell me about a project where laboratory operations was part of your work. What did you do?
- Tell me about a project where assay validation was part of your work. What did you do?
Adapt your resume
- List these exact terms on your resume: Gmp Analytical Testing, Raw Material Testing, Cell Therapy, Laboratory Operations, and Assay Validation. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
Want an expert to read your CV for this job?
Free. Send your CV and the role you want next. We reply by email within 2 to 4 business days.
Get new AI jobs by email
One email a week with the new AI jobs, each rated for how much AI is in the work. No recruiter spam, unsubscribe in one click.
Free. One email a week. Unsubscribe in one click.
Similar roles
Other roles that involve little AI, at other companies.
What kind of AI work fits you?
Answer 12 practical questions in about three minutes. Get a simple profile, the work it points to, and live roles to explore next.
Find my next step