QA Associate

Description

Introduction
The QA Associate will be responsible for managing documentation, coordinating activities of staff,
and monitoring the production of regulatory compliant product. The QA 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 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 licensed cannabis extraction facility located in SW Ontario.
Motif operates as a business-to-business enterprise, offering toll processing and contract manufacturing services to LicensedProducers (LP's) and 3rd Party Brands.

Motif is experiencing significant growth and we are seeking dynamic and professional individuals to join our team.
Motif prides itself on Integrity, Collaboration and Quality, and these core values are at the center of everything we do.

Position Overview:

• Ensure completeness and accuracy ofQAdocumentation, ensuringGood 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 inaccordance with established procedures
• Investigate and complete deviation reports, complaints, and CAPAs
•Review batch records and Certificates of Analysis, ensuringthat product meets quality andregulatory 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 Diplomain science ora related discipline
• Minimum 1 year of experience working in Quality Assurance in a  GMP/GPP environment ,pharmaceutical and/or food and beverage industry
•  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