BioLife Plasma Services
This role involves partnering with Global Regulatory Leads to establish and maintain global regulatory project plans, ensuring the seamless execution of Global Regulatory Team goals for oncology programs. The position requires leading cross-functional submission working groups to deliver successful filings with Health Authorities while providing strategic oversight and operational support for assigned assets. The role focuses on driving project management leadership, managing vendor deliverables, and facilitating continuous improvement within the regulatory affairs organization.
Headquarters
Bannockburn, Illinois, United States
Company Size
5001-10000 employees
BioLife Plasma Services operates a network of plasma collection centers that collect donated human plasma used to manufacture life‑saving plasma‑derived therapies. The company focuses on donor safety and convenience, offering screening, regulated collection procedures, appointment scheduling, and compensation/rewards to encourage repeat donations. BioLife partners with biopharmaceutical manufacturers and maintains rigorous quality and regulatory standards to supply plasma for treatments such as immune deficiencies, bleeding disorders, and other therapeutic uses.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
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