Job Expired
This posting has expired and applications are no longer being received and this job does not show up on the main job list.
This posting has expired and applications are no longer being received and this job does not show up on the main job list.
Job Description
QC Packaging Coordinator
Description
IntroductionThe QA Packaging Coordinator is responsible for ensuring that all Quality standards are being met in the Packaging department. This role ensures the required training and SOP updates are completed for both existing and new products skus to ensure consistent product quality to specification. The scope includes preforming product quality audits on the production lines, performing reviews of production practices to identify continuous improvement opportunities, ensuring production paperwork is complete and accurate, etc. This role also leads timely investigations for any quality deviations; completing a root cause analysis and determining the actions required for long term mitigation. The QA Packaging Coordinator will be responsible for ensuring Good Production Practices (GPP) and all applicable regulations laid out by the Cannabis Act are adhered to at all times. They will be reporting directly to the Quality Assurance Department. The extraction facility is located in Aylmer, Ontario.
?
Company
Motif Labs is a licensed cannabis extraction facility located in SW Ontario. Motif has 3 top-selling internal brands BoxHot, Floresense and Debunk. As well as operating a business-to-business enterprise, offering toll processing and contract manufacturing serviced to Licensed Producers (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, these core values are at the center of everything we do.
?
Position Overview
- Develop and steward thorough training plans for Supervisors, Leads and Production Associates on SOPs for both new and existing products
- Perform regular production audits to confirm adherence to SOPs and GPP
- Review and contribute to Packaging department SOPs to ensure continuous compliance with GPP and adequate consideration for QA, especially for new products and changes to existing products
- Review Packaging Work Orders to ensure accuracy and completeness; provide feedback and training to Leads as required when gaps are identified
- Conduct investigations for quality deviations and CAPAs; complete root cause analysis, determine required mitigations, and hold responsible parties accountable for completing mitigations by an acceptable deadline
- Identify continuous improvement opportunities for quality assurance
- 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
- 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
- Ability to read and correctly interpret documents such as safety rules, regulations, and specifications
- Strong written and verbal communication skills
- Flexibility to work varying shift schedules including weekends. Schedule outlined below.
- Previous work experience with a Canadian Licensed Producer (LP)
- Knowledge of the Cannabis Act, GPP, and GMP
- Experience working in a HACCP environment
- Experience working in a high growth environment