Job Details

A company is looking for an RCA Specialist to manage deviation investigations and quality events in a remote contract position.Key ResponsibilitiesLead end-to-end deviation investigations including data review, gap identification, root cause analysis, and closure in Veeva EQMSReview investigation packages to ensure sufficient supporting data justifies conclusions and identify incomplete investigationsCollaborate within a small remote unit, adapting responsibilities between initiating investigations, writing, and closing based on workloadRequired Qualifications4 to 7 years of GMP quality assurance experience, preferably in biopharma manufacturingHands-on experience writing and closing deviations and CAPAs in a regulated commercial manufacturing environmentExposure to sterile injectable or aseptic processing is a plusProficiency or familiarity with Veeva EQMSAbility to work independently with minimal ramp-up time