Quality Control Analyst
- Baie-D'Urfé, QC
- On-site
- Posted Sep 26, 2026
- 1 position
$30–$33 / hour
Opens an external site
- Employment type
- Contract
- Experience level
- Senior · 5+ years
- Apply by
- Oct 24, 2026
- Posting language
- English
- Working hours
- 40 hours per week
- Seniority
- Mid-Senior level
- Application method
- Direct apply is available
Job summary
Prepare samples and perform laboratory analyses using approved methods, then enter, interpret, verify, and document results accurately. Report and assess non-conformances and deviations, propose corrective and preventive actions, conduct peer reviews, support method optimization and validation, train employees, and assist with investigations.
Job details
Contract Duration: 1 year The Quality Control Analyst position is divided into three distinct areas of responsibility: Chemistry Microbiology Sample Processing Center (CTE) The employee is responsible for carrying out sampling and analytical activities while respecting established priorities and deadlines. These activities include: Preparing samples for analysis and performing analytical techniques using laboratory equipment in accordance with approved methods and specifications. Performing analyses within their area of expertise while ensuring a high first-pass success rate and maintaining accurate, thorough documentation. Interpreting analytical results by: Entering analytical data; Applying calculation methods described in procedures; Interpreting results; Verifying the consistency and accuracy of results. Reporting non-conformances and deviations, evaluating them, and proposing corrective and preventive actions (CAPAs). Independently performing peer review and verification of all activities within their area. Participating in working groups and projects aimed at optimizing analytical methods. Carrying out method transfer or method validation assignments with minimal supervision. Training new employees on activities within their area of responsibility. Providing support to the Quality Control Specialist and the QC Manager during investigations and deviation management. Performing any other duties as required
What you’ll do
Prepare samples and perform laboratory analyses using approved methods, then enter, interpret, verify, and document results accurately. Report and assess non-conformances and deviations, propose corrective and preventive actions, conduct peer reviews, support method optimization and validation, train employees, and assist with investigations.
Requirements
The posting does not specify formal education, years of experience, or other minimum qualifications. It indicates that the analyst should be able to perform work independently within their area of expertise, carry out method transfers or validations with minimal supervision, and maintain accurate documentation and a high first-pass success rate.
Listed skills
- Documentation · Preferred
- Data entry · Preferred
Other relevant skills
Identified from the job description. Confirm important requirements above.
- Sample Preparation
- Laboratory Analysis
- Analytical Techniques
- Laboratory Equipment
- Approved Methods
- Data Entry
- Result Interpretation
- Quality Verification
- Documentation
- Non-Conformance Reporting
- Deviation Management
- Corrective And Preventive Actions
- Peer Review
- Method Optimization
- Method Transfer
- Method Validation
Job areas
- Science & Research
- Manufacturing
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