QC Reviewer - Eurofins BioPharma Product Testing Toronto Inc.
Core
Review laboratory documents and data for finished products, bulk materials, raw materials, and stability studies to ensure compliance with GMP requirements and data integrity.
Role type
Quality Control Reviewer
Builds
CoA releases and compliant laboratory documentation
Domain
Pharmaceutical / Biopharma / GMP
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GMP compliance, data integrity, OOS investigations, CAPA, regulatory audits, analytical instrument knowledge (GC, HPLC, UV, IR, ICP-MS/OES), electronic systems (LIMS), SOP adherence
Preferred skills
Quality Assurance audit background
Technologies
LIMS, GC, HPLC, UV, IR, ICP-MS/OES
Responsibilities
Review lab documents for GMP compliance, verify data accuracy in LIMS prior to CoA release, lead or participate in OOS investigations, complete CAPA, participate in internal/regulatory audits, assist team with documentation and coaching, support regulatory inspections, implement process improvements, follow up on analyst corrections, input data for KPIs
Seniority
Mid-level, hands-on IC
