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. #J-18808-Ljbffr

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