Description
The role operates and maintains manufacturing equipment, documents cGMP-compliant operations, executes equipment and validation protocols, maintains standard operating procedures and batch records, reviews process deviations, supports continuous improvement, troubleshoots equipment, and maintains training compliance. It requires 0–3 years of experience in a cGMP biopharmaceutical manufacturing environment, an A.A.S. in a scientific discipline or equivalent experience, English proficiency, MS Office knowledge, and the ability to work independently and as part of a team in a fast-paced environment.
