Address
Form of work
SalaryThe 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.
With millions of square feet of licensed production capacity and operations spanning four continents, 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 looking for a very well organized and detail-oriented individual to join our quality team. If you have sound judgment, great time management, we want to hear from you!
Responsibilities
- Training new Quality Assurance team members on CMO procedures
- Collaborate with Quality Control, Regulatory Affairs, Operations, and Marketing departments to ensure compliance with Health Canada regulations and guidelines
- Lead review and enforcement to Canadian and EU cGMP
- Revise and create Standard Operating Procedures that align to CMO initiatives according to the Change Control procedure in the Quality Management System
- Tracking and trending Lot Release and KPI data
- Compiling and reviewing CMO Lot Release reports
- Reviewing CMO Transfer documents
- Participating in internal and external audits when required
- Working collaboratively with members of the Manufacturing team to improve processes and optimize productivity
- Ensuring timely response to potential Lot Release impact with corrections and associated timelines
- Supporting continuous improvement projects
- Other duties as assigned
Experience
- Degree or diploma in biology, biotechnology, pharmacology or related field (or equivalent working experience)
- Minimum 3 years’ experience in a quality role
- Working knowledge of Good Documentation Practices, Good Manufacturing Practices and Cannabis Regulations considered an asset
- Experience reviewing and revising regulated documents
- Experience working in an ISO:9001 or GMP environment considered an asset
- Experience in a fast-paced working environment
- Time management, organization and problem solving abilities
- Working knowledge of Microsoft Office Suite
- Experience with ERP systems (Sage or SAP) considered an asset
- Strong verbal and written communication skills
Other Details
This is a full-time role based out of Smiths Falls, ON.
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.
