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Intellectt Inc

Validation Engineer - CQV

Toronto, ON, Canada

$50 to $55 CAD / hour · Contract

Within 25 km of Vaughan · About 10.6 km from the city centre

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Job details

Pay: $50 to $55 CAD / hour
Job type: Contract
Apply by: Nov 19, 2026
Posted: Oct 20, 2026

Original job description

Job Title: Validation Engineer (CQV)

Company: Intellectt Inc.

Location: North York, Ontario, Canada

Employment Type: Contract - 12+ Months

Job Responsibilities

Execute commissioning, qualification, and validation (CQV) activities for pharmaceutical, biotechnology, and other regulated manufacturing facilities.
Develop, review, and execute validation documentation, including User Requirements Specifications (URS), Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.
Support equipment qualification, process validation, utility qualification, and facility commissioning activities in accordance with project requirements.
Prepare and review validation protocols, test scripts, summary reports, deviations, and other quality documentation.
Collaborate with engineering, quality assurance, manufacturing, and project teams to ensure equipment and systems meet design specifications and regulatory requirements.
Support FAT/SAT, commissioning tests, protocol execution, discrepancy resolution, and corrective actions as required.

Required Qualifications

Bachelor's degree in Engineering, Life Sciences, Biotechnology, Chemistry, or a related technical discipline.
Experience in Commissioning, Qualification, and Validation (CQV) within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
Knowledge of equipment qualification, utility systems, process validation, and commissioning methodologies.
Experience developing and executing IQ/OQ/PQ protocols and preparing validation reports.
Familiarity with GMP requirements, quality systems, change control, deviation management, and risk-based validation approaches.

Pay Scale

Anticipated hourly pay range: To be determined based on experience, qualifications, and applicable Canadian employment requirements.

Benefits: Employees hired into this position are eligible for the following benefits, subject to the applicable plan terms and eligibility requirements.

Health Insurance: Medical, dental, and vision insurance options are available through a third-party provider. Employees are responsible for paying the full cost of their insurance premiums.

Retirement Benefits: Retirement savings plan is available. No employer matching or other employer contributions are provided.

Paid Time Off (PTO): No PTO other than that required by applicable provincial and local laws.

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More about this job

Responsibilities

Execute commissioning, qualification, and validation activities for regulated manufacturing facilities, including equipment, processes, utilities, and facilities. Develop and review protocols and quality documentation, support FAT/SAT and testing, resolve discrepancies, and collaborate with engineering, quality, manufacturing, and project teams.

Requirements

A bachelor's degree in engineering, life sciences, biotechnology, chemistry, or a related technical discipline is required. Candidates need CQV experience in a regulated manufacturing environment, knowledge of qualification and commissioning methods, experience with IQ/OQ/PQ protocols and reports, and familiarity with GMP, quality systems, change control, deviations, and risk-based validation.

Skills

Commissioning
Qualification
Validation
Equipment Qualification
Process Validation
Utility Qualification
Facility Commissioning
Validation Documentation
IQ/OQ/PQ Protocols
Design Qualification
FAT/SAT
GMP Requirements
Quality Systems
Change Control
Deviation Management

Benefits

Health Insurance
Retirement Savings Plan
Legally Required Paid Time Off

Visa sponsorship

Not detected in the job text

Keywords

Commissioning
Qualification
Validation
CQV
Pharmaceutical Manufacturing
Biotechnology
Regulated Manufacturing
Design Qualification
Installation Qualification
Operational Qualification
Performance Qualification
Equipment Qualification
Process Validation
Utility Qualification
Facility Commissioning
Validation Protocols
Test Scripts
Validation Reports
FAT/SAT
GMP
Quality Systems
Change Control
Deviation Management
Risk-Based Validation
Corrective Actions

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