Peggy Crowder
Associate Director, Quality - Cell & Gene Therapy @ AstraZeneca
- Role
- Associate Director, Quality - Cell & Gene Therapy at AstraZeneca
- Location
- Philadelphia, PA, US
- LinkedIn followers
- 500 followers
About Peggy Crowder
At AstraZeneca, my focus lies in elevating the quality of life for patients through meticulous quality oversight in Cell & Gene Therapy Apheresis, Cryopreservation, and Infusion Centers. This role builds on a robust foundation from my tenure at the American Red Cross, where I honed my skills in client relationship management and therapeutic solutions.My mission is to forge innovative cellular solutions that address complex clinical challenges. Working alongside cross-functional teams, we strive to advance the field of Cellular Therapy, ensuring safe and effective treatments for those in need. Through research collaboration and a commitment to compliance and auditing, our efforts are geared towards setting new standards in the biopharmaceutical industry.
Experience
Associate Director, Quality - Cell & Gene Therapy
Apr 2024 — Present · US
In this role I will provide Quality oversight to Cell and Gene Therapy Apheresis, Cryopreservation, and Infusion Centers.
Education
McCarrie School of Health Sciences and Technology
Medical/Clinical Assistant
1988 — 1999
The University of Arizona Global Campus
Bachelor of Arts - BA, Non-Profit/Public/Organizational Management
2024
Skills
- Leadership
- Perioperative Autotransfusion
- Regulatory Affairs
- Change Control
- Program Management
- Therapeutic Apheresis
- Quality System
- 21 Cfr Part 11
- Hematology
- Operations Management
- Clinical Research
- Capa
- Quality Auditing
- Management
- Team Building
- Training
- Education Management
- Project Implementation
- Project Coordination
- U.s. Food and Drug Administration (Fda)
- Quality Control
- Gmp
- Biomedical Engineering
- Healthcare
- Sop
- Fda
- Biotechnology
- Corrective and Preventive Action (Capa)
- Validation
- Laboratory
- Cellular Therapy
- Quality Assurance
- Standard Operating Procedure (Sop)
- Software Documentation
- Fda-Good Tissue Practices-21 Cfr 1271
- Quality Management
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