Ellen Wofford

Programs Administrator Ii, Global Medical Affairs Programs, Biopharma at Grifols

Ellen Wofford is a seasoned professional with extensive experience in regulatory affairs and quality assurance within the biotechnology and pharmaceutical sectors. Currently serving as a Senior Regulatory Specialist-Licensing at Grifols, Ellen has held various positions, including Regulatory Affairs Specialist at Grifols (formerly Talecris Plasma Resources) and Corporate Regulatory Compliance/CAPA Specialist at Talecris Plasma Resources. Prior experience includes being a Senior QA Document Control Specialist at Diosynth and a Documentation Specialist at Glaxosmithkline, showcasing a strong background in regulatory compliance, documentation, and quality assurance processes.

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