Jobs in Vaughan, ON and nearby

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

47,970 listings · 6,802 employers Counted Sep 23, 2026. How we count

About these jobs

Employers hiring include Loblaw Companies Limited (749 listings), Scotiabank (669 listings), RBC (551 listings).

Common roles: Software engineer, Retail sales associate, Project manager.

6,715 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	85,000.00	4,048
CAD / hour	23.50	1,927
USD / year	120,000.00	351
USD / hour	25.00	117
CAD / week	1,250.00	15
GBP / hour	35.00	14

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, 29% hybrid, 70% 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 Vaughan, ON and nearby

Within 25 km

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Rang Technologies Inc

Cleaning Validation Coordinator

Whitchurch-Stouffville, ON, Canada

Pay: $30 to $40 CAD / hour
Job type: Contract
Apply by: Oct 23, 2026
Posting language: English
Posted: Sep 23, 2026

Apply About employer

Applications open in a new tab.

Original job description

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 Teva site is required.

“We are an equal opportunity employer. It is our policy to provide employment, compensation, and other benefits related to employment without regard to race, color, religion, sex, gender, national or ethnic origin, disability, veteran status, age, genetic information, citizenship, or any other basis prohibited by applicable federal, state, or local law.”

Apply About employer

More about this job

Responsibilities

Assist with cleaning validation studies, including sampling, data review, results evaluation, periodic reviews, and preparation of protocols and reports. Maintain inspection-ready documentation, coordinate work across departments, support investigations and risk assessments, and help improve cleaning procedures and validation practices.

Requirements

A bachelor’s degree in science, engineering, pharmacy, or a related discipline is required, along with one to two or more years of relevant experience, preferably in pharmaceuticals. Candidates should have working knowledge of GMP/GLP and regulatory requirements, pharmaceutical manufacturing and packaging, relevant software and systems, and strong organizational and prioritization skills; some travel to other Teva sites is required.

Skills

Cleaning Validation
Equipment Swabbing
Rinse Sampling
Validation Documentation
GMP Compliance
Data Review
Risk Assessment
FMEA
Deviation Investigation
CAPA
Change Control
Data Trending
Cross-Functional Coordination
Time Management
Microsoft Office
LIMS

Visa sponsorship

Not detected in the job text

Keywords

Cleaning Validation
GMP
GLP
cGMP
Health Canada
FDA
EMA
WHMIS
Equipment Swabbing
Rinse Sampling
FMEA
Risk Assessment
Gap Assessment
Deviation Investigation
CAPA
Change Control
LIMS
Knowledge Tree
TrackWise
Veeva
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Adobe Reader
Outlook
Pharmaceutical Manufacturing
Packaging Processes
Worst-Case Products
Validation Protocols
Validation Reports

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