Join Cronos Group in Stayner, ON, as a GMP Specialist focused on quality assurance in the cannabis sector. Lead GMP system improvements for our international operations.
As a GMP Specialist, your role is crucial in maintaining and advancing quality compliance in a licensed marijuana facility. You will develop validation plans and documentation that align with regulatory requirements across North America and the EU. Collaborating with teams in Quality Assurance and Production, you will ensure that our processes are audit-ready and adhere to best practices.
Key Responsibilities:
• Oversee GMP implementation for various clients
• Collaborate on validation protocols and project timelines




• Conduct validation lifecycle management and CAPA investigations
• Train staff on GMP processes and compliance
• Ensure documentation meets all regulatory standards
Requirements:
• Diploma or degree in relevant scientific discipline
• 2-5 years experience in regulated industries
• Proficient in writing validation documentation
• Solid knowledge of GMP compliance
• Excellent project management and communication skills
Leverage your GMP skills at Cronos Group and contribute to our mission in the cannabis industry.
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📌 Quality Assurance GMP Specialist Role (Barrie)
🏢 Cronos Group
📍 Barrie