About this role
Grow your quality career in cell therapy at a leading biotechnology company in Boston, Massachusetts. You will investigate manufacturing and QC deviations, find root cause and drive CAPAs to closure. What you'll do Investigate standard-complexity deviations with interviews, GEMBA and root cause analysis tools.
Propose CAPAs with SMEs; manage records in eQMS and meet due dates. Support change controls and effectiveness checks. Track deliverables and escalate risks to the team lead.
Bachelor's degree in Engineering or related + 2–5 years. Pharma/biotech quality, manufacturing or engineering experience. Deviation/CAPA experience and eQMS. Clear technical writing.
Contract: 12 months, with possible extension Shift: On-site; shift set by the hiring manager (may be non-standard) Start: Immediate