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You will be updated with latest job alerts via email GLP Compliance Monitoring: Ensure all QC activitiesincluding sample handling testing equipment usage and result recordingadhere to GLP guidelines.
Documentation Review: Review logbooks worksheets calibration records test reports and analytical data for accuracy and traceability.
Deviation & Incident Handling: Support investigation and closure of GLP deviations non-conformities and laboratory incidents with appropriate CAPAs.
Training & SOP Implementation: Train analysts on GLP principles data integrity (ALCOA) and documentation protocols.
Internal Audits & Inspection Readiness: Conduct self-inspections and ensure lab preparedness for regulatory audits (USFDA MHRA WHO EU-GMP).
Change Control & Quality Systems: Participate in change control risk assessments and continuous improvement initiatives within the QC lab.
Instrument Usage Oversight: Ensure instruments are used calibrated and maintained according to GLP and manufacturer guidelines.
Required Experience:
Senior IC
Full-Time