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Computer Validation Jobs in Ontario (NOW HIRING)

Scotiabank

Manager, Model Validation & Approval

Toronto, ON · Hybrid

  • Medical

  • Retirement

The Manager in the Model Validation & Approval valuation team provides independent and consistent ... Advanced degree in a quantitative field such as Mathematics, Physics, Computer Science, Financial ...

Amd

Post Silicon Validation Manager

Thornhill, ON · Hybrid

Knowledge of computer hardware architecture (CPU/APU, x86, PCIe, memory, bus logic) and software ... Experience developing validation methodologies and infrastructure. * Test plan and test development ...

Alstom

SCC Verification & Validation Designer

Toronto, ON · On-site

CA$80K - CA$105K/yr

  • Medical

  • Life

  • Retirement

Could you be the full-time Integrated Control Center (ICC) Verification & Validation (V&V) Designer ... 105,000 CAD per year, plus benefits and eligibility for an annual performance bonus. Final ...

VitalBio

Verification and Validation Engineer

Oakville, ON · On-site

CA$60K - CA$75K/yr

Participate in design reviews to assess design verification and validation impact; * Accurately ... Familiarity with CAD software (SolidWorks), prototyping equipment (CNC, 3D printing, laser cutter ...

Parsons

CAD Manager & CDE Admin

Markham, ON

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The CAD manager /CDE administrator is required to possess strong computer CAD/BIM and technical ... Quality assurance compliance and validation * Collaboration, coordination and clash/clearance ...

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All JobsComputer Validation JobsComputer Validation Jobs in Ontario

Computer Validation information

What is the difference between Computer Validation vs Quality Assurance Specialist?

AspectComputer ValidationQuality Assurance Specialist
Required CredentialsGxP, 21 CFR Part 11, validation certificationsISO standards, QA certifications, GxP knowledge
Work EnvironmentPharmaceutical, biotech, regulated industriesManufacturing, healthcare, regulated industries
Employer & Industry UsageRegulated industries requiring validated systemsEnsuring quality compliance across processes

Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.

Is computer validation a good field?

Computer validation is a specialized field within quality assurance and regulatory compliance, focusing on ensuring that computerized systems meet industry standards such as 21 CFR Part 11. It often requires knowledge of validation protocols, testing, and documentation, and can offer stable employment opportunities in regulated industries like pharmaceuticals and biotech. The field values certifications and technical skills, making it suitable for professionals interested in compliance, quality systems, and technology validation.

What are popular job titles related to Computer Validation jobs in Ontario?

For Computer Validation jobs in Ontario, the most frequently searched job titles are:

What job categories do people searching Computer Validation jobs in Ontario look for?

The top searched job categories for Computer Validation jobs in Ontario are:

What cities in Ontario are hiring for Computer Validation jobs?

Cities in Ontario with the most Computer Validation job openings:

Computer Validation jobs near you
Infographic showing various Computer Validation job openings in Ontario as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, 2% Contract, and 1% Nights. Highlights an 76% Physical, 2% Hybrid, and 22% Remote job distribution.

Quality Assurance Associate Consultant - Pharmaceutical

Q&C

Mississauga, ON • On-site

Full-time

Re-posted 6 days ago

Job description

This Pharmaceutical Consulting role focuses on applying your GMP knowledge and experience to various projects, such that the client is confident in the approach and timing of execution of the project. Our consultants work independently within a team environment to ensure activities are undertaken in a timely manner.

We are looking for consultants who want to apply their in-depth quality and compliance knowledge and out-of-the-box thinking to challenging projects with our clients. Our projects cover, but are not limited to: deviation investigations, auditing, management of quality systems, delivering of training, batch document review, product releases, equipment validation, computer validation (including data integrity): related to the fabricating, packaging and testing of pharmaceuticals, biologics, NHPs and Medical Devices. Depending on your experience and career goals, the successful candidate would be placed in one of the two operational companies : Q&C Services - focuses on supporting importing projects where importing experience is an asset OR QCR - supports various quality consulting roles.

In this broad-based role, you will support the projects assigned to you, meeting the client's needs. The role specifically prioritizes, plans, organizes and executes projects related to quality and compliance of health products to ensure smooth implementations. The role may involve coordinating/working with client personnel to meet project goals.

Reporting to the Manager, Quality Services or Compliance Services the Associate Consultant is responsible for:

  • Prioritizing and managing compliance projects
  • Completing critical assessments of data and documents to identify gaps compared to regulatory requirements
  • Communicating project milestones on a monthly basis
  • Completing client assigned tasks: deviation investigations, review of importer documentation
  • Developing documentation as required by the project: SOPs, protocols, reports, APQRs etc.
  • Releasing product to market
  • Assisting with hosting Health Canada audits, corporate audits, and self inspections

If you are a Quality Assurance professional in the Pharmaceutical industry, we have the environment and exposure to the type of work you want to do.

Requirements

Education - Bachelors' degree in Science required

1 - 3 years industry experience in the following is an asset:

  • Change/CAPA management
  • Deviation investigations
  • Master manufacturing/batch record review and lot release
  • Annual Product Quality Reviews
  • Stability review and assessment
  • APQR review and assessment
  • Exposure to Health Canada audits, corporate audits and self inspections

Salary range: CAD 60,000 - 70,000 annually

Annual salary will be based on candidate's experience, skill, knowledge, and qualifications relevant to the role.

This posting is for an existing vacancy.

Benefits

Learn about what makes our company unique at www.qualityandcompliance.com

Q&C welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selections process.

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