Responsibilities:
Support the development of medical devices and laboratory equipment and consumables by executing assigned tasks alongside engineers and scientists.
Perform hands on lab activities including device assembly, prototyping, component fabrication, rework, and test setup and execution.
Assist with the creation and maintenance of engineering documentation, such as drawings, DHF docs, bills of materials (BOMs), assembly instructions, and inspection forms.
Plan and execute builds and test builds in the lab, including coordinating activities with internal teams and external vendors when directed.
Develop test protocols and perform engineering experiments, verification & validation tests, accurately record data and observations, and write test reports.
Manage setup, operation, and maintenance of lab equipment and test fixtures, ensuring equipment readiness and proper documentation.
Support manufacturing and pilot build activities by executing handson assembly operations and developing procedures to support daily workflow.
Collect, organize, and summarize experimental and test data for reports and presentations.
Follow and help establish quality, safety, and documentation procedures, including design controls and good documentation practices.
Collaborate closely with crossfunctional teams, including engineering, manufacturing, quality, supply chain, and biology teams, to support daytoday lab and development activities.
Interact with suppliers and thirdparty vendors by preparing materials, parts, or documentation as needed.
Support continuous improvement by identifying opportunities to improve lab workflows, test methods, and equipment organization.
Perform lab support tasks such as inventory tracking, material preparation, labeling, and organizing workspaces.
Qualifications:
Bachelor’s degree and 4+ years of experience, preferably in a related field (electromechanical or medical devices) OR Associate's Degree or College Diploma and 6+ years of experience, or 8+ years of experience.
Able to utilize computer-based equipment control and data collection systems
Basic familiarity with medical device development or regulated environments is a plus.
Experience or coursework involving handson lab work, such as device assembly, prototyping, testing, or fabrication.
Ability to follow written procedures and protocols carefully and maintainaccurate records.
Strong attention to detail
Proficiency with CAD software (SolidWorks or similar)
Comfortable using common laboratory tools, fixtures, and measurement equipment.
Good organizational skills and ability to manage multiple assigned tasks independently.
Effective verbal and written communication skills for documenting work and collaborating with team members.
Demonstrated curiosity, reliability, and enthusiasm for learning new technical skills in an R&D setting.
Working knowledge of measurement equipment such as vision systems, manual height gages, general inspection tools.
Knowledge of design control systems such as ISO 13485 and FDA Quality System Regulation nice to have.
Technologist, Device Development • Toronto, Ontario
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