Job Opportunity: Quality & Production Associate at Carbon Extracts
Position Overview
Carbon Extracts is seeking a
Quality & Production Associate
to join our team and assist in the manufacturing and quality assurance of premium cannabis products. This role requires a strong understanding of
Good Production Practices (GPP), Good Manufacturing Practices (GMP), and Good Documentation Practices (GDocP)
to ensure compliance with
Health Canada regulations
. The selected candidate will play a vital role in production, quality control, and regulatory compliance, ensuring our products meet the highest industry standards.
Key Responsibilities
The
Quality & Production Associate
will work cross-functionally with
Production, Quality Assurance (QA), and Regulatory Affairs (RA)
teams to uphold compliance with
the Cannabis Act, the Cannabis Regulations, and internal quality standards
. The role will focus on:
Production & Manufacturing:
Assist in the preparation and processing of cannabis materials according to established
Standard Operating Procedures (SOPs)
.
Assist in the shipping and receiving of cannabis and production materials.
Monitor production parameters (temperature, humidity, pressure) to ensure product consistency and quality.
Ensure proper handling, storage, and documentation of cannabis products to maintain compliance with
Health Canada
regulations.
Maintain cleanliness and sanitation of the production area in accordance with
GPP, GMP, and quality standards
.
Participate in team meetings and contribute to continuous improvement initiatives.
Quality Assurance & Regulatory Compliance:
Ensure compliance with regulatory frameworks.
Review and approve
batch records, specifications, quality events, deviations, and change management records
in the corporate
Quality Management System (QMS)
.
Conduct quality release activities, ensuring
Certificates of Analysis (CoA)
are within specifications and batch documentation complies with regulatory requirements.
Manage incoming quality control of materials, bulk, packaging, and labeling components.
Identify and investigate
non-conformities, deviations, and adverse events
, performing root cause analysis and implementing
Corrective and Preventive Actions (CAPA)
.
Work closely with
third-party partners, approved labs, suppliers, and Health Canada
during audits and inspections.
Oversee the implementation and operational effectiveness of the
sanitation program
and participate in change management initiatives affecting production quality.
Monitor key quality metrics and contribute to the development of quality improvement strategies.
inventory management, documentation practices, and regulatory frameworks
.
Ability to lift and move materials up to
50 lbs
.
Must be comfortable working in a
fast-paced, highly regulated environment
.
It is preferred if the selected candidate is a QAP (Quality Assurance Person) approved by Health Canada.
Skills & Competencies:
Strong attention to detail and ability to perform repetitive tasks with precision.
Excellent organizational and documentation skills.
Ability to work independently and as part of a
cross-functional team
.
Experience operating and troubleshooting production equipment.
Strong communication skills and ability to train and mentor team members in
GPP/GDocP best practices
.
Demonstrated integrity, discretion, and good judgment in a compliance-driven environment.
Work Schedule
Shift:
Days (8:00 AM to 4:00 PM). Monday-Friday.
Job Type:
Full-time, in-person. No employee benefits currently.
How to Apply
Applications must be submitted through
Indeed
. Only candidates selected for an interview will be contacted.
Job Type: Full-time
Pay: $55,000.00-$75,000.00 per year
Schedule:
Monday to Friday
Weekends as needed
Work Location: In person
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