Intermediate Deviation Writer – Pharmaceutical Production

Deviation Writer
Toronto, ON

Working for a vaccine production department and for the quality control department responsible for in vivo, biochemical and physicochemical tests on vaccines during production and release

– Document  underlying causes and root case of deviations via interviews, GEMBA, 5Whys, Ishikawa, Pareto or Process Mapping
-Document potential consequences
-Document plan to implement CAPAS
-Drafting deviations

Qualifications

Experience in Production and Manufacturing, Quality Assurance, QMS, supply chain, RCA, CAPAs, QMS SAP

Fields of expertise :
Pharmaceutical industry
QA Operations & Systems
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