Systems QA Specialist

Flosonics Medical; Toronto; On-site; CAD 70,000 - 90,000; Full time

Job summary

Flosonics Medical is seeking a skilled Systems QA Specialist to enhance safety in medical technology. This role involves working on a range of projects, developing and executing detailed testing strategies, and collaborating with cross-functional teams. Applicants should have a solid educational background in engineering or technology and 3-5 years of relevant QA experience in the medical devices sector.

Qualifications

• 3-5 years of experience in system-level QA roles required.
• Experience with manual and automated testing protocols is critical.
• Knowledge of medical device regulations is advantageous.

Responsibilities

• Generate and document verification plans for future releases.
• Execute detailed test protocols based on requirements.
• Produce formal reports for verification results.

Skills

Scripting skills

Automated testing

Verification documentation

Python

Quality Assurance

Education

Bachelor's degree in electrical engineering

Bachelor's degree in computer science

Bachelor's degree in human factors engineering

Bachelor's degree in medical technology

Tools

Robot Framework

Appium

Matlab

Octave

R

Job description

Join to apply for the Systems QA Specialist role at Flosonics Medical.

We are seeking an experienced Systems QA Specialist with a strong background in the medical technology industry to join our team. You will work closely with our development team to create and execute feature, integration, and end-to-end tests. You will use your QA expertise to help us make safe and effective medical devices.

In this role, you will have the opportunity to work on a variety of projects, including the development of new products and the improvement of existing systems. You will need to have a strong understanding of system, software, cloud, and hardware verification principles and techniques, as well as experience with building automated testing tools and frameworks.

Responsibilities:

• Generating and documenting high-level verification plans for future releases including regression, integration, and functional strategies.
• Generating and executing detailed comprehensive low-level manual and automated test protocols based on requirements.
• Performing and producing formal documented reports for the results of verification protocols for software, embedded systems, hardware, mechanical, production tools, and cloud components.
• Evaluating and modifying requirements to ensure testability and appropriate measurement tolerance.
• Identifying and documenting changes to specifications during planning by soliciting input from SMEs.
• Configuring and maintaining test hardware, jigs, and diagnostic equipment to support testing efforts.
• Working in a cross-functional team to improve the scope and efficiency of device-level testing in manufacturing.

Qualifications and Education Requirements:

• Bachelor’s degree or higher in electrical engineering, computer science, human factors engineering, medical technology, or similar.
• Minimum 3-5 years working experience in a system-level QA role.
• Deep understanding of building and executing both manual and automated test protocols covering all levels of systems including electrical, mechanical, embedded, cloud, and application software.
• Strong scripting/coding skills for developing test protocols and small utility functions.
• Experience working with numerical computation using Python, Matlab, Octave, or R is beneficial.
• Proficiency with developing formal verification documentation in a regulated industry to support clearance. Knowledge of medical device regulations is an advantage.
• Experience testing systems transmitting over wireless or unreliable communications channels.
• Experience using Robot Framework and Appium to create automated tests for iOS applications.
• Experience with testing application software, electrical, mechanical components, and embedded systems.

We thank all applicants; however, only those selected for an interview will be contacted. Accommodations are available upon request to meet accessibility needs.

Seniority level

• Associate

Employment type

• Full-time

Job function

• Quality Assurance

Industries

• Medical Equipment Manufacturing

This job posting is active and available.