Betsy Williams has a wealth of experience in quality, compliance, and regulatory consulting in the pharmaceutical, medical device, and healthcare industries. With a background in engineering, validation, project management, and leadership, Betsy has held various roles in companies such as GSK US and Validant, where Betsy has successfully managed global projects and led validation efforts for sterile manufacturing processes. Williams has also worked as a Senior Quality Engineer at STERIS Infection Prevention Technologies and as a QA Supervisor/QA Manager at Johnson & Johnson, showcasing their expertise in quality control and process engineering.
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