The purpose of this role is to support the GMP production of viral therapeutics through aseptic processing, including cell culture, purification, formulation, and fill/finish activities. This position is also responsible for maintaining cleanroom environments, preparing buffers and components, and ensuring adherence to cGMP standards and documentation practices.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree