Job Description
Responsibilities :
Perform all manufacturing operations under cGMP/ISO requirements
Display understanding of Upstream process theory (e.g., incubation, expansion, cell growth, harvest) equipment operation, and aseptic processing
Assist with the installation, commissioning, and validation of equipment within single use facility
Adhere to manufacturing procedures and documentation as well as identifying clarifications or updates when required
Perform legible, clear, and concise data entry into batch records, logbooks, and all other ancillary controlled forms used in a cGMP process
Maintain a high level of quality and compliance with regards to all aspects of manufacturing
Assist/write SOPs (standard operating procedures), batch records, and other GMP documentation
Display ability to identify and escalate potential GMP issues, as required
Available to participate in flexible shift...
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Submit ApplicationJob Details
- Location Sanford, North Carolina
- Job Type Full-time
- Category Drafters, Engineering Technicians, and Mapping Technicians
- Posted Date June 23, 2026
- Application Deadline August 02, 2026