Quality Assurance At-the-Source Specialist, Cell Therapy — US - Rockville - MD
AstraZeneca · US - Rockville - MD
Posted Posted 14 mins ago
Refyne take
This Quality Assurance At-the-Source Specialist, Cell Therapy role at AstraZeneca was posted in the last 5 days. Before applying, run your resume through the checker on the right — most rejections here are keyword and formatting mismatches, not qualifications.
Job Profile Description
Provides independent, visible Quality Assurance leadership at the source of cell therapy manufacturing. This is a shift-based role scheduled for four days per week, Wednesday through Saturday. Partners with Manufacturing and supporting functions to apply risk-based quality judgment, resolve issues within established frameworks, and support reliable, compliant execution. Operates independently across qualified routine and moderately complex situations, influences cross-functional decisions, and strengthens quality culture through practical coaching, clear communication, and disciplined follow-through. Specific quality-system responsibilities and approval authorities are defined through applicable procedures, qualifications, and delegated authority.
This is a shift-based role scheduled four days per week, Wednesday through Saturday .
Typical Accountabilities
• Maintain a consistent Quality presence in manufacturing areas and provide real-time, practical guidance that supports safe, compliant, and reliable execution.
• Support manufacturing unit operations from a Quality Assurance perspective and assist to resolve manufacturing events and/or quality events in real-time
• Independently assess routine and moderately complex quality situations, integrate available facts and risk considerations, and determine appropriate action or escalation within established standards.
• Partner across functions to clarify requirements, align decisions, remove barriers, and sustain appropriate Quality independence.
• Recognize emerging risks, recurring issues, and performance gaps; communicate implications and recommend proportionate actions.
• Lead defined problem-solving and improvement activities, ensuring decisions are evidence-based, clearly documented, and carried through to effective resolution.
• Coach colleagues on quality thinking, disciplined execution, data integrity, contamination control, and right-first-time behaviors.
• Contribute quality judgment to operational meetings, shift handoffs, readiness discussions, and cross-functional decision forums.
• Manage multiple priorities independently, communicate changes in risk or urgency, and maintain reliable follow-through in a fast-paced patient-focused environment.
• Support inspection readiness and represent Quality confidently within the scope of training, experience, and delegated authority.
• Work a shift-based schedule of four days per week, Wednesday through Saturday, and support occasional off-hours or holidays as needed for manufacturing operations and patient commitments.
• The role may require additional responsibilities as necessary.
Qualifications and Skills
QA ATS Specialist Required Education and Experience:
• 5+ years applicable quality experience with B.S. degree in Science, Engineering or related technical field
• 9+ years applicable with Associates degree
• 13+ years applicable with High School Diploma
• Proven ability to work in a fast-paced environment across multiple technical functions
• Strong knowledge of cGMPs
• Demonstrated ability to make decisions under pressure that balance patient safety, compliance and supply
Preferred Experience:
• Autologous cell therapy manufacturing or quality experience
• Working knowledge of international Cell Therapy GxP regulatory frameworks, regulations and guidance
The annual base pay for this position ranges from $79,890 - $119,835. Our positions offer eligibility for multiple 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
21-Oct-2026
Closing Date
03-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.
Explore related searches
Browse the wider category, city and company pages this role belongs to.
Similar qa engineer jobs
Other openings posted in the last five days that match this role.
- Test Engineering Intern Spring 2027Rocket Lab · Wallops Island, VAonsiteentryQuick applyPosted 18 mins ago
- Test Engineering Intern Summer 2027Rocket Lab · Wallops Island, VAonsiteentryQuick applyPosted 18 mins ago
- Senior Electrical Hardware Test Engineer, Energy StorageRedwood Materials · San Francisco, California, United StatesonsiteseniorQuick applyPosted 19 mins ago
- Abuse Test Engineer, Energy StorageRedwood Materials · McCarran, NVonsitemidQuick applyPosted 19 mins ago
- Quality Assurance, Post Market SpecialistStryker · Redmond, WashingtonhybridmidPosted 25 mins ago
- Senior QA EngineerEpic Games · BLANK,BLANK,Multiple LocationsonsiteseniorQuick applyPosted 25 mins ago
More jobs at AstraZeneca
- Process Engineer - Night ShiftAstraZeneca · US - Coppell-Texas - TXonsitemidPosted 1 day ago
- Director, Clinical AI Delivery OperationsAstraZeneca · US - Gaithersburg - MDonsiteleadPosted 1 day ago
- Quality Assurance SpecialistAstraZeneca · US – Santa Monica Colorado Avenue – CAonsitemidPosted 1 day ago
- Senior Equipment Engineer, Cell TherapyAstraZeneca · US - Rockville - MDonsiteseniorPosted 1 day ago
- Director, Oncology Commercial Data Science & AI ProductsAstraZeneca · US - Gaithersburg - MDonsiteleadPosted 2 days ago