However, you can amend your search to find:
Review and evaluate clinical data generated from the imaging portion of sponsor clinical trials across various therapeutic areas. Maintain organized, complete, and up-to-date study documentation in accordance with internal and regulatory standards.
Driving all aspects of purification process development, characterization, and technology transfer to cGMP manufacturing for hybrid and continuous processes; Serving as an internal technical resource for cGMP manufacturing and Process Design as well as a
This person will join a fast-paced, collaborative, and multidisciplinary team to support purification process development at the bench and pilot scale for the advancement of low-cost biotherapeutics manufacturing. Experience with high throughput
Contribute to the design of novel and efficient synthetic pathways for drug substances undergoing clinical development; Conduct and oversee route scouting in laboratory to demonstrate synthetic viability; Use all imaginable chemistry tools and methods to