Medical laboratory quality expertise meets regulatory compliance in this in-person Technical and Regulatory Quality Specialist contract. Support operations through technical troubleshooting and quality systems leadership.

This 18-month contract runs approximately through February 2028, with possible extension subject to business needs. You will advise Operations and Patient Services while supporting accreditation readiness, inspections, audits, and continuous quality improvement. The work connects laboratory methods, equipment, supplies, documentation, and regulatory requirements.

Key Responsibilities:

- Troubleshoot methodologies, equipment, supplies, and quality systems
- Maintain policies, procedures, processes, and forms
- Prepare regulatory inspections, assessments, and internal audits




- Implement validation protocols for technologies and procedures
- Monitor nonconformances and corrective action plans

Requirements:

- Medical Laboratory Technology diploma or equivalent education and experience
- Current CMLTO or CSMLS registration, according to province
- Minimum three years of previous laboratory experience
- Solid regulatory compliance and quality systems knowledge
- Excellent technical writing and communication skills

Apply medical laboratory expertise, audit readiness, validation, and quality systems knowledge to strengthen regulatory compliance and operations.

📌 Medical Laboratory Quality Specialist (Toronto)
🏢 Lifelabs
📍 Toronto