QA Reviewer - Eurofins BioPharma Product Testing Toronto, Inc.
Core
Ensuring compliance with ISO 17025 and GMP regulations by reviewing quality documents, managing audits, and investigating deviations for biopharma product testing.
Role type
Quality Assurance Reviewer
Builds
Compliance reports, audit documentation, and quality system procedures for biopharma clients
Domain
Life Sciences / Biopharma / Laboratory Testing
Deliverable
dashboards & analysis
Required skills
ISO 17025 knowledge, GMP experience, deviation investigation, CAPA management, change control, document management, audit support, data evaluation, SOP adherence
Preferred skills
Science-related degree, MS Office proficiency, proactive work style
Technologies
MS Office (Outlook, Word, Excel)
Responsibilities
Review and determine status of quality documents (raw data, validation studies, logbooks, calibration reports), assist with internal and external audits, log and review complaints, initiate and conduct deviations and OOS investigations, initiate and conduct CAPA investigations, initiate and assist in Change Control procedures, manage tracking and maintenance of GMP and ISO 17025 documents, support training of new staff, evaluate and summarize instrumentation data in final reports
Seniority
Individual Contributor
