Audit batch records and release products as a Quality Assurance Associate with Teva in Stouffville, Ontario, working Tuesday through Saturday day shifts.This 12 month contract supports on floor quality assurance and product release. You will review manufacturing, packaging, and testing documentation, maintain compliance with GMPs and SOPs, and evaluate quality incidents. The work includes electronic data review, deviation investigations, CAPAs, and cross functional communication. Experience with TrackWise, Oracle or SAP, LIMS, and Microsoft Office supports the position.Key Responsibilities:Audit batch records and release bulk or finished goodsComplete final identification samples and audit noticesInvestigate deviations and determine product impact, root cause, and CAPAsPerform GMP audits, environmental monitoring,



and documentation reviewsPrepare quality shift reports and communicate batch release queriesRequirements:Canadian university science degree or recognized equivalentOne year relevant Quality Assurance experience; three preferredWorking knowledge of TrackWise, Oracle, SAP, LIMS, and Microsoft OfficeKnowledge of GMPs, SOPs, GDP, and data integrityMechanical aptitude and ability to analyze moderately complex problemsApply quality assurance, GMP compliance, documentation review, and product release expertise to support Teva operations in Stouffville.#J-18808-Ljbffr

📌 Qa Associate - On The Floor & Product Release - 12 Month Contract, Afternoon Shift (Whitchurch-Stouffville)
🏢 Teva
📍 Whitchurch-Stouffville