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Quality Control Technician (Contract)
Charlottetown, Prince Edward Island, Canada
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About the Opportunity


Our client is a growing manufacturing organization specializing in contract manufacturing, bottling, and packaging solutions within a regulated production environment. They support customers in bringing natural health and consumer products from development through commercial production while maintaining a strong focus on quality, compliance, and continuous improvement.

We are currently seeking a Quality Control Technician for a contract assignment in Charlottetown, PEI. This role is responsible for supporting quality operations by performing inspections, testing, documentation, and ensuring products are manufactured in accordance with GMP, food safety, and quality standards.


What Success Looks Like

  • Accurate and timely completion of raw material, in-process, and finished product testing
  • Effective identification and control of non-conforming products
  • Consistent compliance with GMP and quality standards throughout production areas
  • Complete and accurate quality documentation and records
  • Strong collaboration with production teams to maintain product quality and safety


Key Responsibilities


Product & Raw Material Testing

  • Perform quality testing on raw materials, packaging materials, in-process products, and finished goods, including:
  • pH testing
  • Brix testing
  • Product weight verification
  • Label verification
  • Moisture and water activity testing
  • Other quality-related assessments as required
  • Complete quality checks and approvals for incoming ingredients and packaging materials prior to production use
  • Assist with sampling of raw materials and finished products according to established procedures
  • Support product release activities through quality management systems
  • Conduct final quality checks on finished products prior to shipment
  • Maintain retain samples for raw materials, packaging components, and finished products
  • Compile, review, and interpret quality testing results and documentation


Quality Documentation & Corrective Actions

  • Identify, document, and control out-of-specification (OOS) or non-conforming products
  • Work closely with Production Supervisors to investigate quality issues and implement corrective actions
  • Escalate quality concerns appropriately to ensure risks are effectively managed
  • Complete inspection reports, quality records, and documentation accurately and in accordance with Good Documentation Practices (GDP)


GMP Compliance & Facility Quality Monitoring

  • Monitor production, packaging, and warehouse areas to ensure compliance with GMP standards
  • Verify production documentation and product requirements prior to manufacturing activities
  • Support facility quality programs including:
  • Housekeeping standards
  • Cleaning and sanitation verification
  • Personal hygiene compliance
  • Pest control monitoring


Environmental Monitoring & Equipment Verification

  • Perform routine verification and documentation of quality equipment, including:
  • Scales
  • Thermometers
  • pH meters
  • Refractometers
  • Metal detectors
  • Laboratory equipment
  • Support sanitation verification activities, including ATP swabbing and rinse water sampling
  • Maintain environmental monitoring records and quality documentation
  • Assist with air and water quality testing programs to ensure compliance with GMP and regulatory requirements


Qualifications


Education & Experience

  • Diploma or degree in Food Science, Biology, Chemistry, Life Sciences, or a related discipline
  • Knowledge of HACCP principles and food safety practices
  • Experience with Quality Control or Quality Assurance processes within a GMP manufacturing environment
  • Previous experience in food, pharmaceutical, natural health product, or regulated manufacturing environments considered an asset


Technical Skills

  • Strong computer skills with proficiency in Microsoft Office applications
  • Experience with quality documentation systems or manufacturing software considered an asset


Core Competencies

  • Strong attention to detail and accuracy
  • Excellent written and verbal communication skills
  • Ability to prioritize tasks and manage time effectively
  • Strong organizational skills and ability to work independently
  • Ability to collaborate effectively with production and quality teams


Working Conditions

  • 12-hour shifts, including days and nights
  • Standing and walking for extended periods on hard surfaces
  • Ability to lift up to 30 lbs.
  • Work performed in a manufacturing environment that may include:
  • Noise
  • Temperature variations
  • Production equipment
  • Required PPE


Contract Opportunity


This is a contract position offering the opportunity to gain experience within a regulated manufacturing environment while supporting a growing organization focused on quality and operational excellence.

Our Commitment to Inclusive Hiring


We are committed to providing an inclusive and accessible recruitment process. We welcome applications from candidates of all backgrounds and experiences. Accommodations are available throughout the recruitment process upon request.

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