QA-QC Associate

Introduction

The QA/QC Associate will be responsible for managing documentation, coordinating activities of staff, and monitoring the production of regulatory compliant product. The QA/QC Associate will provide assistance to the functions within the Quality Management System, and will be dedicated to ensuring compliance across all departments. Reporting to the QA Supervisor, the QA/QC Associate will be responsible for ensuring that Good Production Practices (GPP) and all applicable regulations laid out by the Cannabis Act are adhered to at all times. The extraction facility is located in Aylmer, Ontario.

Company

Motif Labs is a leading cannabis brand house in Canada, proudly holding top market share positions in vapes and infused pre-rolls. As the largest private cannabis business in Canada, our diverse portfolio of winning brands (BOXHOT, DEBUNK, Rizzlers and Floe State) are each thoughtfully curated to meet the dynamic and evolving needs of today's consumer market. Motif Labs is dedicated to maintaining the highest standards of quality, ensuring that our products not only meet but exceed the expectations of our clients and consumers alike.

Position Overview:

• Ensure completeness and accuracy of QA documentation, ensuring Good Documentation Practices on all applicable documents related to GPP
• Assist with managing the Quality Management System
• Draft SOPs to ensure continuous compliance
• Ensure that cannabis, raw materials, and packaging materials are received and tested in accordance with established procedures
• Investigate and complete deviation reports, complaints, and CAPAs
• Review batch records and Certificates of Analysis, ensuring that product meets quality and regulatory requirements
• Ensure that all staff are adhering to facility SOPs and GPP at all times
• Work with QA Supervisor to develop, implement and conduct internal facility audits as scheduled
• Other job duties as assigned

Qualifications:

• Bachelor’s Degree or College Diploma in science or a related discipline
• Minimum 1 year of experience working in Quality Assurance in a GMP/GPP environment, pharmaceutical and/or food and beverage industry
• Knowledge of the Cannabis Act, GPP, and GMP
• Experience working in a HACCP environment
• Experience with Quality Systems: Change Control, Deviation, CAPA, Document Control
• Ability to work in a dynamic environment and collaborate with a cross-functional project team
• Highly organized with attention to detail for successfully satisfying diverse responsibilities
• Ability to read and correctly interpret documents such as safety rules, regulations, and specifications
• Strong attention to detail, ensuring documentation is complete and accurate
• Strong written and verbal communication skills
• Flexibility to work varying shift schedules

Nice to Have's:

• Previous work experience with a Canadian Licensed Producer (LP)
• Experience working in a high growth environment

The selected candidate for this role will be required to work onsite in Aylmer. Applicants must be legally entitled to work in Canada and currently reside in the country, as we do not offer sponsorship.

Motif Labs welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.