About The Position

We're hiring a Quality Assurance Co-op to join our QA team and support the day-to-day operation of our ISO 13485-compliant quality management system. This is a generalist role designed to give you broad exposure to MedTech quality — investigations, audits, document control, training, design and change control, and data analysis — inside a real, regulated environment. You'll work alongside our QA team and partner closely with manufacturing, R&D, and regulatory affairs. By the end of the work term, you'll have a strong foundation across the QA discipline and a clearer sense of which corner of it you want to grow into.

Requirements

  • Working towards a technical degree (engineering, sciences, etc.)
  • Strong attention to detail.
  • Clear, professional written communication.
  • Comfortable with AI tools to support day-to-day work and quick to pick up new tools.
  • Solid grounding in foundational stats and experimental design.
  • Curiosity about regulator environments and a willingness to ask “why” before jumping to “how”.
  • Python for data analysis.

Nice To Haves

  • Prior experience in medical devices, pharma, or other regulated industries.
  • Exposure to ISO 13485, 9001.
  • Familiarity with Atlassian tools.
  • Familiarity with root cause analysis methods.

Responsibilities

  • Support non-conformance (NCR) and CAPA investigations, including root cause analysis and effectiveness checks.
  • Assist with internal audits and external audit preparation (MDSAP, ISO 13485, Health Canada CMDR, FDA 21 CFR Part 820/QMSR).
  • Administer the eQMS day-to-day: assign and track training, manage records, follow up on overdue items.
  • Support change control and design control activities (ECOs, design history file maintenance, traceability).
  • Pull, clean, and analyze quality data to surface trends across NCRs, complaints, and audits.
  • Help develop and improve SOPs and work instructions.
  • Document everything in accordance with ISO 13485:2016 and applicable regulatory requirements.
  • Contribute to process improvement projects across QA, manufacturing, and R&D.

Benefits

  • Compensation: The pay for this position will be based on average co-op wages as outlined by your academic institution’s co-op program or similar institutions if specific data is unavailable, ensuring fair and competitive compensation aligned with industry and academic standards. The typical range for this role is $22 - $25 per hour for work terms 2-4.
  • Grant Eligibility: This position is made possible through wage subsidy grants such as BioTalent SWPP. As such, participants must be a current full-time student registered in a Canadian Post-secondary program. International students are not eligible. Eligible participants must be a Canadian citizen, permanent resident or person who has been granted refugee status in Canada and be legally entitled to work.
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