Apply hands-on quality assurance expertise with Curaleaf International in Brampton, supporting GMP compliance and production standards. Work 40 hours weekly on a Sunday-to-Wednesday or Wednesday-to-Saturday schedule.
As an In Process QA Associate, you will maintain quality across a regulated production facility. You will conduct floor checks, support sampling, manage labels, and review documentation. The role works closely with manufacturing, cultivation, and cross-functional teams to identify quality issues and support practical solutions.
Key Responsibilities: Perform gowning, hygiene, cleanliness, line clearance, and in-process checks
Collect samples and coordinate timely Certificates of Analysis
Print production labels and complete required approvals accurately




Review batch records, logbooks, SOPs, and worksheets
Support deviations, CAPAs, change controls, and audit readiness
Requirements: Post-secondary degree in science or related discipline
At least two years’ QA experience in production
GMP experience or GMP certification
Robust communication and collaboration skills
MS Office experience, particularly Excel
Bring production-floor quality checks, documentation accuracy, and GMP knowledge to Curaleaf International’s Brampton facility while supporting compliant operations.

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📌 In Process Quality Assurance Associate (Ontario)
🏢 Curaleaf International
📍 Ontario