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Computer System Validation Jobs in Ontario (NOW HIRING)

NXP Semiconductors

... system analysis; Work design and verification teams in root causing the issues. Gain deep ... The candidate must have a Bachelor's degree in Computer Science or Computer Engineering.

1Valet

Systems Analyst - Technical Support

Toronto, ON · Remote

Perform remote diagnostics, testing, and system validation for software and hardware installations ... Support and troubleshoot computer networks, including IP addressing, switches, PoE devices, and ...

Actalent

Software Test & Validation Engineer

Markham, ON · On-site

CA$40 - CA$50/hr

Anticipate potential test and system issues, proactively recommend solutions, and contribute to ... Solid computer skills and familiarity with engineering test methodologies and automation frameworks.

1Valet

Field Technician Support

Orleans, ON

Perform remote diagnostics, testing, and system validation for software and hardware installations ... Support and troubleshoot computer networks, including IP addressing, switches, PoE devices, and ...

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Computer System Validation information

See Ontario salary details

$25

$47

$78

How much do computer system validation jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for computer system validation in Ontario is $47.68, according to ZipRecruiter salary data. Most workers in this role earn between $35.58 and $57.21 per hour, depending on experience, location, and employer.

What are some typical challenges faced in Computer System Validation roles?

Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.

What is a Computer System Validation job?

A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.

What are the key skills and qualifications needed to thrive in the Computer System Validation position, and why are they important?

To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.

What are popular job titles related to Computer System Validation jobs in Ontario? For Computer System Validation jobs in Ontario, the most frequently searched job titles are:
What job categories do people searching Computer System Validation jobs in Ontario look for? The top searched job categories for Computer System Validation jobs in Ontario are:
Computer System Validation jobs near you

Validation Engineering Associate

Prollenium Medical Technologies Inc.

Richmond Hill, ON

Other

Posted 9 days ago

Job description

JOB SUMMARY:

The Validation Specialist supports the manufacturing team by performing process valuations on new and current manufacturing processes. This position reports to the Senior Director of Manufacturing.


MAJOR RESPONSIBILITIES:

  • Conduct validation, temperature mapping, and calibration activities
  • Measure instruments, software performance and machine performance to determine operating as defined and required
  • Establish and maintain methods to control the biomanufacturing processes and develop effective ways to monitor product performance, and analyze data
  • Generate, execute and review qualification and validation studies according to approved protocols and SOPs (Standard Operating Procedures)
  • Write protocol documents and reports to show how each biomanufacturing system, piece of equipment, method, software or process is validated
  • Analyze the results of testing and determine their acceptability against predetermined criteria
  • Adhere to strict documentation, reviews and approvals. Investigate and troubleshoot problems and determine solutions or recommendations for changes and improvements, including expanding facilities and upgrading equipment and software


ADDITIONAL RESPONSIBILITIES:

  • Provide validation related support to other departments and leaders
  • Other duties as assigned


MINIMUM QUALIFICATIONS:

Technical Knowledge/Experience

  • Bachelor's degree in science or engineering
  • Knowledge of and experience with GMPs (Good Manufacturing Process).
  • Knowledge of and experience with Validation programs, Installation qualification (IQ), Operational Qualification (OQ) Performance qualification (PQ)
  • Knowledge of and experience with DOE (Design of Experiment)
  • Knowledge of and experience with various statistical analysis and statistical tools
  • Documented experience with technical report preparations in English
  • Experience with problem solving skills, Gage R and R, cPK analysis, OEE, control charts. FMEA, Risk Analysis, CAPA
  • Working knowledge of ISO 13485-2016, 21 CFR and various regulating agencies: Health Canada, FDA and EU
  • Proficient command of the English language, both written and verbal


Behavioural

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

  • Teamwork: Ability to work independently and effectively and productively with others
  • Communication: Understand and follow verbal and written instructions
  • Problem Solving: Anticipating, analyzing, diagnosing and resolving problems
  • Organization and Planning: Utilizing logical, systemic and orderly procedures to meet objectives
  • Flexibility: Ability in adapting to change

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