Quality Assurance Specialist

Cronos is an innovative global cannabinoid company committed to building disruptive intellectual property by advancing cannabis research, technology, and product development.

With a passion to responsibly elevate the consumer experience, Cronos is building an iconic brand portfolio.

Cronos’ diverse international brand portfolio includes Spinach®, PEACE NATURALS® and Lord Jones®.

For more information about Cronos and its brands, please visit: https://thecronosgroup.com/ .

At Cronos Group, we hire talented people who thrive on solving difficult problems and give them the opportunity to hone new skills and approaches.

If you want to play a part in shaping an innovative industry and help build a historically significant company, we want to meet you.

As a QA Specialist you will work within the Quality Assurance department to support product release in Canada and International markets.

The QA Specialist completes tasks related to monitoring, testing, reporting, and ensuring quality of cannabis product and processes with the Company’s Quality Management System (QMS).

This position supports in the area of batch record review, supplier quality, customer complaints, internal and external audits, compliance requirements, metrics and reporting, and maintaining the QMS and applicable governing regulations throughout the Company.

This position is based out of Stayner, ON

What you’ll be doing:

• Maintain compliance with the laws and regulations related to cannabis products released to Canada and International markets
• Develop and execute procedures and processes to support Quality Management System
• Support problem solving teams using quality principals and tools for root cause analysis, corrective actions, verification and effectiveness
• Conduct complaint and deviation investigations, and ensure appropriate Corrective Action and Preventative Action (CAPA) are implemented and closed in a timely manner
• Work with other cross functional groups to review and assess change controls
• Conduct review and support activities related to QA records including but not limited to deviations, CAPAs, batch record review, label approvals, and other related Quality Management Systems (QMS).
• Liaise with external suppliers and contract manufacturing organizations and review supplier documentation to ensure Quality and Company requirements are met and maintained.