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Internship Computer System Validation Csv Jobs in Toronto, ON

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 ... generators, optical systems, computer vision, machine learning; * Advanced level analytical ...

1Valet

Junior QA Engineer

Toronto, ON · On-site

... on 1VALET Entry systems and related hardware. * Assist in validating hardware integrations ... internships, hands-on projects, or lab coursework). * Foundational understanding of hardware ...

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 ...

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 ...

Waabi

Research Internship/Co-op

Toronto, ON

CA$45 - CA$60/hr

... systems. - Be encouraged to submit and publish work externally at top machine learning, computer ... Application Instructions: - To be considered for an internship/co-op, please add your most up to ...

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All JobsComputer System Validation Csv JobsInternship Computer System Validation Csv JobsInternship Computer System Validation Csv Jobs in Toronto, ON

Internship Computer System Validation Csv information

What is an internship in computer system validation (CSV)?

An Internship in Computer System Validation (CSV) is a temporary position, typically for students or recent graduates, that provides hands-on experience in ensuring that computer systems used in regulated industries (like pharmaceuticals or healthcare) meet required standards and regulations. Interns assist with validating software and hardware, documenting processes, and ensuring compliance with industry guidelines such as FDA 21 CFR Part 11 or EU Annex 11. This role helps interns understand the lifecycle of computer systems in a regulated environment and prepares them for careers in quality assurance, compliance, or IT within highly regulated sectors.

What is the difference between Internship Computer System Validation Csv vs Computer System Validation Specialist?

AspectInternship Computer System Validation CsvComputer System Validation Specialist
CredentialsTypically pursuing or recent graduate, basic understanding of validationRelevant certifications (e.g., GAMP, ISPE), experience preferred
Work EnvironmentInternship setting, supervised, entry-level tasksFull-time role, independent responsibilities in regulated industries
Industry UsageUsed in pharmaceutical, biotech, and medical device companies for trainingUsed for maintaining compliance, validating systems in regulated environments

In summary, the Internship Computer System Validation Csv is an entry-level position focused on learning and supporting validation tasks, while the Computer System Validation Specialist is a more experienced role responsible for ensuring system compliance and validation in regulated industries.

What are the key skills and qualifications needed for an internship in computer system validation (CSV)?

To thrive as an Internship Computer System Validation CSV specialist, you need foundational knowledge in computer science, life sciences, or engineering, along with an understanding of regulatory standards like GxP or FDA 21 CFR Part 11. Familiarity with validation documentation, software testing tools, and quality management systems is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for interpreting requirements and collaborating with cross-functional teams. These skills ensure compliance, data integrity, and the successful validation of computerized systems in regulated environments.

What are the typical responsibilities of an intern in computer system validation (CSV)?

As a Computer System Validation (CSV) intern, you can expect to assist with tasks such as reviewing and drafting validation documentation, executing test scripts, and collecting evidence to ensure compliance with regulatory requirements. You may also support the maintenance of validation records and participate in team meetings to discuss project progress or findings. These responsibilities are crucial in ensuring that computer systems used in regulated industries, like pharmaceuticals or healthcare, function as intended and meet quality standards. Working closely with senior validation specialists, you'll gain hands-on experience with industry guidelines and learn how cross-functional teams collaborate to achieve compliance.
What are popular job titles related to Internship Computer System Validation Csv jobs in Toronto, ON? For Internship Computer System Validation Csv jobs in Toronto, ON, the most frequently searched job titles are:
What job categories do people searching Internship Computer System Validation Csv jobs in Toronto, ON look for? The top searched job categories for Internship Computer System Validation Csv jobs in Toronto, ON are:
Internship Computer System Validation Csv jobs near you
Infographic showing various Internship Computer System Validation Csv job openings in Toronto, ON as of August 2026, with employment types broken down into 78% Full Time, and 22% Contract. Highlights an 100% In-person job distribution.

Verification and Validation Engineer

VitalBio

Oakville, ON • On-site

CA$60K - CA$75K/yr

Full-time

Re-posted 28 days ago

Job description

About You:

You possess excellent problem-solving skills and approach every problem with a friendly and positive attitude. You are self-motivated, possess a high level of autonomy, and enjoy working in a highly technical, fast-paced, and multidisciplinary environment. You take ownership of a problem and seek additional information where sufficient input is lacking to proceed with testing and see the problem through to resolution. You take pride in making things work and seeing others effectively use what you worked on.

What You’ll Do:

  • Take ownership of various design verification activities;

  • Design, develop, and execute test plans and procedures;

  • Work closely with the R&D, Engineering, and Quality teams to create a robust test suite;

  • Complete documentation for results and reports;

  • Use exploratory test techniques to provide early testing feedback throughout the design and development process;

  • Design and develop methods and test tools, manual and automated, to aid in efficient and systematic testing;

  • Demonstrated use of reliability and quality engineering methods and tools – DFMEA, life data analysis, reliability testing, statistical analyses, etc;

  • Participate in design reviews to assess design verification and validation impact;

  • Accurately report and track product defects, verify hardware bug fixes, and perform regression testing;

  • Help generate manufacturing instructions and associated in-process test methods, where necessary;

  • Manage test equipment to comply with calibration requirements and perform inspection on equipment.

What You’ll Need:

  • Bachelor’s or Master's degree in Electrical Engineering, Mechatronics Engineering, Biomedical Engineering or equivalent;

  • 3+ years of related experience;

  • 2+ years of professional experience in a team working on new product development;

  • Experience in a regulated industry (specifically medical and aerospace);

  • Hands-on expertise with electrical test and measurement equipment: oscilloscopes (voltage/current/power), multimeters, signal generators, optical systems, computer vision, machine learning;

  • Advanced level analytical programming (Python, Matlab, etc.).

Bonus points for:

  • Experience developing/testing/production of IVD devices;

  • Experience designing specialized electro-mechanical and optomechanical test fixtures;

  • Scripted automated testing (e.g., using Python or JavaScript with Test and Measurement equipment);

  • Familiarity with CAD software (SolidWorks), prototyping equipment (CNC, 3D printing, laser cutter), and general machine shop experience;

  • Knowledge of the following standards: IEC 60601, ISO 13485, ISO 14971;

  • Experience with the medical device product development lifecycle;

  • Appreciation of puns!

The salary range for this position is $60,000-$75,000 annually. Compensation will be determined based on the individual’s demonstrated experience, education, training, relevant certifications or licensure, and other applicable business and organizational factors.

This role is a current, onsite vacancy.

About Vital Bio


Vital is revolutionizing point-of-care diagnostics with our VitalOne platform, delivering real-time care wherever patients are. Our mission is to democratize health technology, making healthcare more accessible and proactive.

Our global team of experts spans chemistry, software, engineering, and microfluidics. We thrive on change, operate on trust, and value diverse perspectives. Our growth-minded culture empowers front-line decision-making and fosters impactful work.

We seek tenacious, bold individuals ready to transform healthcare. At Vital, your talent will make a difference as we work to ensure everyone has access to care when and where they need it.


Vital Biosciences Inc. is an equal opportunity employer and values diversity in the workplace. We are therefore happy to accommodate any individual needs in keeping with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act. If you require accommodation in order to participate in our hiring process, please contact us to make your needs known in advance

As part of our recruitment process, we may use automated or AI-supported tools to assist with application review and screening. These tools are used to support, not replace, human decision-making. Final hiring decisions are always made by our hiring team.