Participate in ancillary validation studies including aseptic process simulations (APS/media fills), equipment performance qualifications (PQ), cleaning validation studies, hold-time studies, container closure integrity testing (CCIT), and other GMP qualification and validation activities. The essential requirements of the job include: Currently pursuing a Bachelor's degree in Chemical Engineering, Bioprocess Engineering, Biomedical Engineering, Biological Systems Engineering, Biotechnology, or a related STEM discipline.