Takeda is a global, values-based, R&D-driven biopharmaceutical leader headquartered in Japan, committed to discover and deliver life-transforming treatments, guided by our commitment to patients, our people and the planet. Within Takeda, the Parenteral Drug Product Development (PDPD) group is responsible for formulation development of synthetic and protein therapeutics from animal toxicity study to human clinical trials as well as commercial launch. The group is also responsible for the development of final drug products as well as developing and scaling manufacturing processes to global manufacturing sites. The summer intern will work with members of the parenteral drug product development group to plan, execute, and analyze laboratory experiments to develop an overall understanding of protein formulation, stability and manufacturing process. The intern will focus on but not limited to the understanding and quantifying interaction between various surfactants and protein biologics using QCM. Through the project, the intern will gain extensive hands-on experience on biophysical and biochemical characterization techniques for biologics including: QCM, Zeta potential, ultraviolet–visible (UV), and Fourier transform infrared (FTIR) spectroscopy, light scattering, light obscuration, and microflow imaging. The intern will also have the opportunity to gain knowledge of laboratory equipment and experience with method development.
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Job Type
Full-time
Career Level
Intern
Number of Employees
5,001-10,000 employees