The Company
At Canopy Growth, our mission is clear: improve lives, end cannabis prohibition, and strengthen communities. We believe that cannabis can be a force for good. We’re building a consumer-centric organization that is focused on sharing the transformational potential of cannabis with the world. We will achieve this through an innovative and disruptive portfolio of cannabis and hemp-derived products.
Canopy Growth is the world's leading cannabis and hemp company. We recognize that employees are at the core of our success, and we take pride in a corporate culture that emphasizes inclusiveness, collaboration, and diversity.
Our employees come from a wide range of backgrounds, each bringing their own unique skills and talents to the table, working together to continue our incredible momentum of growth. If you are interested in building global challenger brands, scaling a business, and working in a values-driven environment, we want to hear from you!
The Opportunity
We are seeking a very well organized and detail-oriented individual to join our quality team. If you have sound judgment and great time management skills, we want to hear from you!
Responsibilities
Creating and submitting batch record packages for lot release in the company QMS and reviewing against company Good Documentation Practices requirements.
Approval of inbound and outbound cannabis shipments
Approval of incoming materials
Participating in investigations and report creation associated with non-conformity events
Support collection and shipping of analytical samples.
Support ongoing environmental monitoring activities (air particle counts and settle plates)
Updating and maintaining documentation within the Quality Management System
Tracking and trending KPI data
Supporting continuous improvement projects
Creating and revising Standard Operating Procedures that align to site and corporate requirements according to the Change Control procedure within the Quality Management System
Other duties as assigned
Experience
Degree or diploma in biology, biotechnology, pharmacology or other scientific field (or equivalent working experience)
Working knowledge of Good Documentation Practices, Good Manufacturing Practices with Cannabis and EU-GMP Regulations an asset
2+ years of Quality Assurance experience
Experience managing or conducting audits considered an asset
Experience reviewing and revising regulated documents
Strong interpersonal and communication skills
Experience in a fast-paced working environment where time management, organization and problem solving were key skills
Working knowledge of Microsoft Office suite of programs
Experience with ERP systems (Sage or SAP) considered an asset
Strong verbal and written communication skills
Strong technical writing skills
Other Details
This is a full-time on-site role based in Tiverton, ON.
Salary Range: $55,000 - $68,000 CAD
Benefits – extended health and dental coverage, paid vacation, and participation in our employer-supported retirement savings program
We appreciate your interest, and promise to review all applications, but we will only be contacting those who best fit the requirements.
We welcome and encourage applications from people with disabilities. Accommodations are available upon request for candidates taking part in all aspects of the selection process. If you require accommodation, please notify your Talent Acquisition Partner. Please note, the chosen applicant will be required to successfully complete background and reference checks.
Recruitment Process: All applications for this role are reviewed manually; no AI-based screening or ranking tools are used.
This post is for an existing vacancy.