Director Quality Assurance

Join us as a Director Quality Assurance , where you will lead and direct the Site Quality Assurance Operations at our Cell Therapy 9950 MCD Rockville manufacturing site. This role offers an opportunity to develop strategic and operational plans, lead high-level projects, and define innovative solutions within complex areas of the business. You will be working on diversified tasks with a global team, providing you with exposure to new ways of thinking and helping us grow collectively and as individuals. What you will do: Lead the new Quality Assurance team at the Commercial Cell Therapy Facility, supporting facility start-up and routine production. Partner with senior leaders across AstraZeneca to ensure delivery of an integrated approach to Cell Therapy Quality. Participate in investigations, assessments, and evaluations of quality records such as deviations, CAPAs, and change controls. Manage, develop, and lead a team of Quality Assurance professionals. Minimum Qualifications: B.S. degree in Science, Engineering, Pharmacy, or related technical field with a minimum of 8 years of applicable experience M.S. degree in Science, Engineering, Pharmacy, or related technical field with a minimum of 5 years of applicable experience Minimum of 5 years of management experience Minimum of 2 years of Cell Therapy/Biologics Quality Assurance experience including clinical lot release Experience with product launches, health authority inspections, and global commercial product distribution requirements Proven ability to work in a fast-paced environment across multiple technical functions. Demonstrated ability to make decisions under pressure that balance patient safety, compliance, and supply. Ability to influence senior stakeholders, both internally and externally Preferred Qualifications: Advanced degree in Science, Engineering, Biochemistry, Pharmacy, or related technical field Minimum of 2 years of Cell Therapy Quality Assurance experience including clinical lot release Demonstrated track record in leadership of change management in a positive and non-disruptive manner to the company’s values. Experience with Cell Therapy regulatory inspections Experience engaging with global regulatory bodies. Proven track record of attracting and developing talent. Extensive working knowledge of international Cell Therapy GxP regulatory frameworks, regulations, and guidance The annual base salary for this position ranges from $174,856 - $262,285 USD. However, 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 include 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 salary (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: 11-Jun-2026 Closing Date: 02-Aug-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. #J-18808-Ljbffr AstraZeneca GmbH