In Process QA Associate

Company Description Curaleaf International is a global cannabis company focused on research-driven, high-quality products across Europe, Canada, and Australasia. The organization operates at every stage of the supply chain, integrating advanced cultivation, extraction, and production with a robust distribution network. Its operations include clinics, pharmacies, laboratories, and EU-GMP certified cultivation and processing facilities in the UK, Portugal, Spain, Germany, Poland, and Canada. The company is experiencing rapid growth while maintaining a strong commitment to quality, safety, and regulatory compliance. Curaleaf International is part of Curaleaf Holdings, Inc., a leading international producer and distributor of consumer cannabis products.

Role Description The In Process QA Associate is a full-time, on-site role based in Brampton, ON, responsible for monitoring and supporting quality activities during manufacturing and packaging operations. The individual will perform in-process checks, verify compliance with SOPs, batch records, and GMP standards, and promptly escalate deviations or non-conformances. Daily tasks include documenting observations, supporting root-cause investigations, and assisting with CAPA implementation to prevent recurrence of quality issues. The role also involves collaborating with production, quality control, and regulatory teams to ensure products meet established specifications and are manufactured in a safe and controlled environment. The In Process QA Associate will contribute to continuous improvement initiatives, participate in internal audits, and help maintain an organized, inspection-ready facility.

Qualifications

• Strong Quality Control and Quality Assurance skills, with experience in in-process checks and GMP-compliant operations.
• Demonstrated Analytical Skills and Quality Management capabilities for evaluating data, identifying trends, and supporting investigations.
• Effective Communication skills for clear documentation, reporting, and collaboration with cross-functional teams.
• Understanding of GMP, GPP, or other regulated manufacturing environments; experience in pharmaceutical, cannabis, or food production is an asset.
• Post-secondary education in science, engineering, quality, or a related field, or equivalent practical experience in a regulated industry.
• High attention to detail, strong organizational skills, and the ability to work accurately under time constraints.
• Proficiency with basic computer applications and electronic quality or documentation systems.