Jobs in Richmond Hill, ON and nearby

Jobs within 25 km of Richmond Hill, ON, Canada. Nearby towns and cities are included. Distances are straight-line, not driving distances.

25,109 listings · 4,707 employers Counted Oct 25, 2026. How we count

About these jobs

Employers hiring include Husky Technologies (1,169 listings), Loblaw Companies Limited (510 listings), Shoppers Drug Mart (425 listings).

Common roles: Retail sales associate, Project manager, Sales representative.

4,409 of these listings include employer-provided pay. Open a job to see its currency and pay period.

Advertised starting pay
Pay period	Median starting pay	Listings
CAD / hour	23.00	2,158
CAD / year	75,000.00	1,826
USD / year	109,000.00	190
USD / hour	18.95	72
CAD / month	4,000.00	10

Employer-listed minimums from at least 10 listings per currency and pay period. These are advertised starting amounts, not employee salaries. Jobs without a minimum and unusual amounts are excluded.

Workplace classifications: 0% remote, 17% hybrid, 83% on-site, 0% not specified. Hybrid and on-site classifications may be inferred from descriptions. Check the original ad.

Based on the dated count above. Listings can change. How we count

Jobs in Richmond Hill, ON and nearby

Within 25 km

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Added 2 days ago
Logistics Supervisor
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CH
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UH
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- Full-time
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UI
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Richmond Hill, ON
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UI
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Markham, ON
- $120,000 to $150,000 CAD / year
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Richmond Hill, ON
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Markham, ON
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Added 2 days ago
LC
Grocery Clerk Part Time Night Greenlight Requisition
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Vaughan, ON
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Added 2 days ago
LC
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Vaughan, ON
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Added 2 days ago
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Added 2 days ago
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Prollenium Medical Technologies Inc.

Quality Control Analyst

Aurora, ON, Canada

$48,000 to $52,000 CAD / year · Full-time

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Job details

Pay: $48,000 to $52,000 CAD / year
Job type: Full-time
Experience: 1-3 years of work experience in a Quality Control Laboratory within a regulated environment (Medical Devices, Pharmaceutical, Cosmetics, etc.)
Posting language: English
Posted: Sep 23, 2026

Original job description

JOB SUMMARY:

The Quality Control Analyst performs routine and non-routine quality control testing of raw materials, in process materials, and finished medical device products. The role supports stability programs, process and method validation, method transfer, and development activities within a regulated Quality Management System (QMS). The Quality Control Analyst contributes directly to product safety, quality, and regulatory compliance throughout the product lifecycle. This role reports to the QC Supervisor.

MAJOR RESPONSIBILITIES:

QC Testing and Documentation

Execute Quality Control activities in compliance with ISO 13485, GMP, GLP, and internal quality system requirements.
Perform routine and non-routine testing of raw materials, in process materials, and finished products in accordance with approved specifications, test methods, and production schedules.
Review, verify, and approve laboratory data, test results, and supporting documentation as per Good Documentation Practices (GDP) and Good Laboratory Practices (GLP)
Support product disposition activities by reviewing test results against acceptance criteria and assisting with batch and material release documentation as per QMS requirements.

Stability, Validations and Investigations

Conduct routine and non-routine tests for stability studies using approved procedures/protocols.
Conduct non-routine testing to support process/equipment validation, investigations, change controls, and other quality related activities as assigned.
Escalate atypical results, conditions and deviations to Supervisor or Sr. QC Analyst
Participate and support investigations such as OOS, Deviations, etc. by performing additional testing, review and root cause problem solving.

QC Support Tasks

Manage QC inventory, including release and status control of materials, reagents, and test articles; ensure traceability of consumables and retention samples.
Ensure laboratory records are prepared, reviewed, and maintained in compliance with document control and record retention requirements.
Assist in drafting, reviewing, and revising SOPs, forms, validation protocols, and reports in accordance with quality system procedures.
Order laboratory supplies and ensure proper receipt, inspection, identification, and labeling of materials.
Perform and document routine laboratory equipment checks and maintenance; report equipment issues per deviation and nonconformance procedures.
Support maintenance, calibration and troubleshooting of laboratory equipment.
Participate in departmental, quality, and cross functional meetings as required.
Perform other duties as assigned to support operations.

MINIMUM QUALIFICATIONS:

Technical Knowledge/Experience

1-3 years of work experience in a Quality Control Laboratory within a regulated environment (Medical Devices, Pharmaceutical, Cosmetics, etc.)
Microbiology experience preferred.
University Degree or greater in a Scientific discipline (Chemistry, Microbiology, Biotechnology or related field)
Good understanding of Good Laboratory Practices (GLP) and Good Documentation Practices.
Working knowledge of analytical techniques (e.g., wet chemistry, HPLC, spectroscopy, chromatography, Endotoxin Testing, PCR, Aseptic Technique).
Strong written and oral communication skills.

Behavioral

Demonstrated ability to apply the following behavioral competencies on the job:

Teamwork: Works effectively within cross functional teams.
Written Communication: Produces clear, accurate, and compliant documentation.
Problem Solving: Identifies, analyzes, and resolves quality related issues under appropriate supervision.
Organization & Planning: Manages tasks methodically to meet timelines and compliance requirements.
Flexibility: Adapts to changing priorities, regulatory expectations, and operational needs.

PREFERRED QUALIFICATIONS:

Experience in a regulated laboratory environment (medical device, pharmaceutical, or Cosmetics).
Exposure to wet chemistry or advanced analytical testing techniques.
Experience with inventory control and material status systems.
Experience preparing or supporting controlled technical documentation (SOPs, protocols, reports)

WORKING CONDITIONS:

Required to work about 50% in a laboratory environment with computer work required to support QMS activities.

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More about this job

Responsibilities

Perform routine and non-routine quality control testing of raw materials, in-process materials, and finished medical device products, and review laboratory data and documentation to support product disposition. Support stability studies, validations, investigations, equipment and inventory control, and the preparation and maintenance of controlled quality records.

Requirements

Requires 1–3 years of quality control laboratory experience in a regulated environment and a university degree or higher in a scientific discipline. Candidates should understand GLP and GDP, have working knowledge of analytical techniques, and demonstrate strong communication, problem-solving, organization, teamwork, and adaptability.

Skills

Quality Control Testing
Good Laboratory Practices
Good Documentation Practices
ISO 13485
Good Manufacturing Practices
Analytical Testing
Wet Chemistry
HPLC
Spectroscopy
Chromatography
Endotoxin Testing
PCR
Aseptic Technique
Root Cause Analysis
Stability Testing
Validation

Visa sponsorship

Not detected in the job text

Keywords

Quality Control
Medical Devices
Quality Management System
ISO 13485
Good Manufacturing Practices
Good Laboratory Practices
Good Documentation Practices
Raw Materials
In-Process Materials
Finished Products
Stability Studies
Process Validation
Equipment Validation
Method Validation
Method Transfer
Wet Chemistry
HPLC
Spectroscopy
Chromatography
Endotoxin Testing
PCR
Aseptic Technique
Out-of-Specification Investigations
Deviation Investigations
Root Cause Analysis
Change Control
Batch Release
Document Control
Equipment Calibration
Inventory Control

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