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© All Rights Reserved. ApplyBlast.com
BioLife Plasma Services
The GRA CMC Product Lead at Takeda leads the execution of regulatory CMC strategies for assigned products throughout their clinical development and commercial lifecycle. This role involves representing the team in Health Authority meetings, guiding regulatory submissions, and ensuring compliance with global regulatory requirements. The position requires strong leadership, analytical skills, and the ability to navigate complex matrix environments to drive regulatory success.
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,
and employee contacts for BioLife Plasma Services.
Director, Global Regulatory Affairs CMC
Takeda Pharmaceutical Company Limited
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