Job Description & How to Apply Below
As a GMP Specialist at Cronos Group, you will lead the development of GMP processes while supporting international customer needs.
Your role will involve creating validation documentation and managing cross-functional teams to ensure compliance with Health Canada and EU regulations. With a focus on continuous improvement and operational efficiency, you'll help shape quality protocols in the cannabis sector.
Key Responsibilities:
• Oversee implementation of GMP processes in cannabis operations
• Create and maintain validation reports and protocols
• Assist in training teams on GMP and validation requirements
• Conduct periodic reviews and validation lifecycle management
• Prepare for mock inspections and audits by organizing documentation
Requirements:
• 2–5 years of experience in regulated industries
• In-depth knowledge of GMP and EU-GMP standards
• Strong project management skills and attention to detail
• Proficient in technical writing and documentation
• Degree in a relevant field like Life Sciences or Engineering
Support quality compliance and drive excellence in cannabis production as a GMP Specialist at Cronos.
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