This application is for a 6-month student role from January - June 2025. Resume review begins in October 2024. The RTP Pharma site supports two sterile filling lines in the Parenteral Fill (PF) facility, a small-scale filling line, an Oligonucleotide Synthesis Manufacturing (OSM) Area, and an Oral Solid Dose (OSD) Manufacturing Area. As a Co-Op in Quality Engineering, the successful candidate will help ensure that Quality systems supporting facility, equipment, automation, and utilities remain in compliance with Biogen and industry cGMP standards. These activities would include support of facility and equipment controls and release from planned shutdowns of the various manufacturing areas, as well as general facility and equipment oversight (e.g., pest control program and calibration/Remedial Action Report program, respectively). 
