Job Description
Step into the GMP Validation Specialist role at Cronos Group located in Stayner, Ontario, focusing on regulatory compliance and quality assurance in the cannabis industry. Lead validation processes that ensure excellence in production.
As a GMP Validation Specialist, you will create and maintain GMP systems vital for operational excellence within our cannabis facility. This role engages you in designing validation protocols that meet stringent standards, fostering strong collaboration with teams like QA, Production, and Regulatory Affairs. You'll play an essential part in upholding quality across domestic and international operations.
Key Responsibilities:
• Develop validation plans and manage execution
• Oversee documentation for GMP compliance
• Support CAPA investigations and resolution
• Conduct periodic reviews of validation processes
• Provide operational teams with GMP and validation training
Requirements:
...
As a GMP Validation Specialist, you will create and maintain GMP systems vital for operational excellence within our cannabis facility. This role engages you in designing validation protocols that meet stringent standards, fostering strong collaboration with teams like QA, Production, and Regulatory Affairs. You'll play an essential part in upholding quality across domestic and international operations.
Key Responsibilities:
• Develop validation plans and manage execution
• Oversee documentation for GMP compliance
• Support CAPA investigations and resolution
• Conduct periodic reviews of validation processes
• Provide operational teams with GMP and validation training
Requirements:
...
Ready to Apply?
Submit your application today and join our talented team at Cronos Group Inc..
Submit ApplicationJob Details
- Location stayner, on
- Job Type Full-time
- Category Management & Operations
- Posted Date June 06, 2026
- Application Deadline July 16, 2026