Quality Control Analyst

Job summary

The QC Analyst is responsible for verifying raw cannabis weights, conducting material inspections, and performing equipment calibrations. They also manage data entry in the ERP system and ensure compliance with Health Canada regulations.

Job details

Quality Control Analyst Charlottetown, PEI About Auxly Cannabis Group Inc. Auxly is a leading Canadian cannabis company dedicated to bringing innovative, effective, and high-quality cannabis products to the wellness and adult-use markets. Auxly's experienced team of industry first-movers and enterprising visionaries have secured a diversified supply of raw cannabis, strong clinical, scientific and operating capabilities and leading research and development infrastructure in order to create trusted products and brands in an expanding global market. Learn more at www.auxly.com and stay up to date at Twitter: @AuxlyGroup; Instagram: @auxlygroup; Facebook: @auxlygroup; LinkedIn: company/auxlygroup/. About the role The Quality Control department is seeking to fill a full time Quality Control (QC) Analyst role. Reporting to the Lead Quality Control Chemist, the QC Analyst will be responsible for a variety of QC tasks including but not limited to: verification of incoming raw cannabis weights, receiving samples into the ERP system (Sage), equipment calibrations, and generating monthly Health Canada Inventory reports. What can you expect to do: Review, edit, format documents from all departments and conduct incoming material inspections. Collaborate with Quality Assurance and conduct quality checks as directed by senior technicians, supervisors. Conduct audits, quality inspections, document verification and testing of raw materials. Use the internal ERP system to update receipt of materials, testing progress, and ordering of materials Review production and packaging logbooks for completion and provide feedback, where applicable. Assist with recurring calibrations on laboratory equipment. Ensure the proper selection, care and use of tools, parts and equipment required for specific tasks. Ensure all working areas including laboratories and counters are adhering to all Health Canada and legislative regulations. Perform all tasks in accordance with all established regulatory and compliance and safety requirements. Other related tasks as required. What we’re looking for: University degree or college diploma 1-3 years of experience in Quality Control in a GMP/GPP environment. Previously demonstrated attention to detail and ability to follow Standard Operating Procedures (SOP's). Previous working experience in receipt of materials (warehousing/shipping) in a controlled environment. Bachelor of Science degree (preferably with a focus in Chemistry) or Bio-Technology diploma Excellent interpersonal and active communication skills. Must demonstrate a positive, “can-do” attitude and a willingness to learn new skills on the job. What will set you apart Previous experience using an ERP or QMS system (Sage) How we hire Auxly Cannabis Group Inc. is an equal opportunity employer and encourages applications from all qualified individuals. We thank all applicants for their interest, however, only those selected for an interview will be contacted. We provide accommodation for job applicants with disabilities during the recruitment process in accordance with applicable laws. Please contact us to request accommodation.

What you’ll do

The QC Analyst is responsible for verifying raw cannabis weights, conducting material inspections, and performing equipment calibrations. They also manage data entry in the ERP system and ensure compliance with Health Canada regulations.

Requirements

Candidates need a university degree or college diploma, preferably a Bachelor of Science in Chemistry or a Bio-Technology diploma. 1-3 years of experience in a GMP/GPP quality control environment is required.

Listed skills

• ERP systems · Preferred
• Quality Control · Preferred
• interpersonal communication · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Quality Control
• GMP/GPP Compliance
• Equipment Calibration
• ERP Systems
• Document Verification
• Material Inspection
• SOP Adherence
• Inventory Reporting
• Laboratory Safety
• Interpersonal Communication

Job areas

• Science & Research
• Manufacturing
• Healthcare
• Logistics