Jobs in Markham, ON and nearby

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

11,834 listings · 2,250 employers Counted Sep 23, 2026. How we count

About these jobs

Employers hiring include Loblaw Companies Limited (177 listings), Walmart Canada (155 listings), WSP in Canada (149 listings).

Common roles: Retail sales associate, Project manager, Personal support worker.

1,589 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 / year	75,000.00	778
CAD / hour	21.58	601
USD / year	93,100.00	82
USD / hour	18.60	36

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, 19% hybrid, 81% 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 Markham, ON and nearby

Within 25 km

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Added 20 hours ago
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PayCruit

Cleaning Validation Coordinator

Whitchurch-Stouffville, ON, Canada

Pay: $34.5 to $43.13 CAD / hour
Job type: Full-time
Apply by: Oct 21, 2026
Posting language: English
Posted: Sep 21, 2026

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Applications open in a new tab.

Original job description

Job title: Cleaning Validation Coordinator

Contract:: 12 Months contract

Shift hours :: Shift Schedule: Fully Onsite - Monday – Friday 8:00 AM – 5:00 PM, 37.5 weekly hours.

Location: Whitchurch-Stouffville, ON L4A 0Y2

*Overtime is given after working beyond 38.75 ST hours.

Key Responsibilities and Primary Duties:

Assist in the preparation, execution, and reporting of cleaning validation studies.
Coordinate/perform equipment swabbing and rinse sampling activities.
Support the collection, review, and organization of cleaning validation data.
Assist in evaluating cleaning validation results against established acceptance criteria.
Support periodic review of cleaning validation programs.
Prepare and revise protocols, reports, risk assessments, and related validation documentation.
Ensure documentation complies with GMP, company procedures, and regulatory requirements.
Support investigation activities related to cleaning validation deviations and excursions.
Maintain validation files and ensure documentation is inspection ready.
Coordinate activities between QA, QC, Operations, Engineering, and MS&T.
Schedule cleaning validation studies around manufacturing activities.
Support risk assessments (FMEA, Risk Assessments, Gap Assessments) related to cleaning validation activities.
Assist in identifying worst-case products and equipment locations.
Support continuous improvement initiatives for cleaning procedures and validation practices.
Help trend cleaning validation results and identify recurring issues.
Maintain compliance with cGMP, Health Canada, FDA, EMA, and internal quality standards.
Participate in investigations, CAPAs, and change controls as required.
Other duties as required.

Position Requirements:

Bachelor’s degree in science, Engineering, Pharmacy or related discipline.
One (1) to Two (2) + years of relevant experience, preferably in the pharmaceutical industry.
Computer literate and proficient in: Microsoft Word, Excel, PowerPoint, Adobe Reader, Outlook Applications, LIMS, and Knowledge Tree, Track wise and Veeva.
Working knowledge of GMP/GLP regulations and other Regulatory requirements for Canadian, US and EU markets, WHMIS, and Safety Precautions.
Knowledge of Manufacturing and Packaging processes in a pharmaceutical environment is preferred.
Time management and organizational skills to multi-task and determine priorities.
Some travel to other Client site is required.

Apply About employer

More about this job

Responsibilities

The Cleaning Validation Coordinator will assist in the preparation, execution, and reporting of cleaning validation studies while ensuring compliance with GMP and regulatory standards. They will also coordinate sampling activities and support investigations, CAPAs, and risk assessments across various departments.

Requirements

Candidates must hold a bachelor's degree in science, engineering, pharmacy, or a related discipline. A minimum of one to two years of relevant experience in the pharmaceutical industry and proficiency in GMP regulations are required.

Skills

Cleaning Validation
GMP
Equipment Swabbing
Rinse Sampling
Risk Assessment
FMEA
Gap Assessment
Regulatory Compliance
Documentation
Data Analysis
Pharmaceutical Manufacturing
Quality Assurance
Quality Control
Time Management
Microsoft Office
LIMS

Visa sponsorship

Not detected in the job text

Keywords

Cleaning Validation
GMP
Pharmaceutical Industry
Equipment Swabbing
Rinse Sampling
Risk Assessment
FMEA
Gap Assessment
Regulatory Compliance
Health Canada
FDA
EMA
Quality Assurance
Quality Control
Manufacturing
Packaging
LIMS
Knowledge Tree
Trackwise
Veeva
WHMIS
CAPA
Change Control
Documentation
Validation Protocols
Data Analysis
Science
Engineering
Pharmacy
Microsoft Office

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