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
- Strong 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.
