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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-2026 Closing Date 22-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. AstraZeneca is a global, science-led, patient-focused biopharmaceutical company. We focus on discovering, developing and commercialising prescription medicines for some of the world’s most serious diseases. But we are more than one of the world’s leading pharmaceutical companies. At AstraZeneca, we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science, challenge convention and unleash your entrepreneurial spirit. To embrace differences and take bold actions to drive the change needed to meet global healthcare and sustainability challenges. There is no better place to make a difference in medicine, patients, and society. An inclusive culture where you will connect different thinking to generate new and valuable opportunities. Where you will find a commitment to lifelong learning, growth and development for all. Our Inclusion & Diversity (I&D) mission is to create an inclusive and equitable environment where people belong, using the power of our diversity to push the boundaries of science to deliver life-changing medicines to patients. Inclusion and diversity are fundamental to the success of our company, because innovation requires breakthrough ideas that only come from a diverse workforce empowered to challenge conventional thinking. We’re curious about science and the advancement of knowledge. We find creative ways to approach new challenges. We’re driven to make the right choices and be accountable for our actions. As an organisation centred around what makes us human, we put a big focus on people. Across our business, we want colleagues to wake up excited about their day at the office, in the field, or in the lab. Along with our purpose to bring life-changing medicines to people across the globe, we have a promise to you: to help you realise the full breadth of your potential. Here, you’ll do work that has the potential to change your life and improve countless others. And, together with your team, you’ll shape a culture that unites and inspires us every day. This is your life at AstraZeneca. Details Details Details 
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Astrazeneca
US - Rockville - MD, United States of America
QC Associate – Global Cell Therapy Raw Materials.
$55.9K–83.9K/HR
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