The CandidateBS.in Engineering, Computer Science, Life Sciences or another related technical discipline with a minimum 6 years of experience within the biopharmaceutical or regulated pharmaceutical industry (previous CDMO experience is a plus).Experience in cell therapy, gene therapy, biologics, aseptic manufacturing, CDMO, or other fast-paced GMP manufacturing environments preferred. This individual will work closely with Validation, Quality Assurance, Facilities & Engineering, Automation/OT, IT, Manufacturing, MSAT, Quality Control, clients, and vendors to manage project deliverables, resolve technical issues, assess risk, support timely system release, and provide technical guidance to developing engineers and cross-functional teams.