Reporting to the Manager, Clinical Manufacturing, this Contractor role will participate in the day-to-day manufacturing of cellular supply for the company’s clinical programs and participate in pre-clinical supply campaigns as required.
As required, participate in the manufacturing environment cleaning program and work to assure all manufacturing suites, equipment and critical environments are cleaned on scheduled and per qualified methods
BS./M.S. in Biology, Bioengineering or related scientific discipline.
1- 2 years’ relevant experience with manufacturing in cGMP environments.
Understanding of federal regulations for Quality Systems (21CFR820) and GMP manufacturing (21CFR 210,211).