About The Position

This position offers an opportunity to begin a challenging and rewarding career at Arjo, a healthcare company dedicated to empowering movement for people with mobility challenges. As a Technical Documentation Specialist, you will play a crucial role in ensuring product documentation complies with regulatory requirements and actively participate in various engineering and quality improvement initiatives.

Requirements

  • Bachelor’s degree in Engineering or Science, combined with relevant experience in a regulated environment, or any equivalent combination of education and experience.
  • Proficiency in English, intermediate to advanced level (4/5).
  • Full proficiency in French (5/5).
  • Strong attention to detail, autonomy, and a keen interest in the technical aspects of products.
  • Excellent analytical skills, critical thinking, and the ability to work effectively as part of a team.

Nice To Haves

  • Experience in the medical field or in a highly regulated industry

Responsibilities

  • Act as the delegate of the Product Development and Engineering Department for the review and approval of product documentation, ensuring that technical files comply with applicable regulatory requirements.
  • Ensure the validation of software under the department’s responsibility (Excel spreadsheets, test benches, internal tools, etc.).
  • Actively participate in engineering projects, product maintenance initiatives, continuous quality improvement activities, cost-reduction efforts, and regulatory compliance projects.
  • Coordinate engineering actions arising from the Quality Management System (non-conformities, audit observations, corrective and preventive actions, etc.).
  • Ensure thorough, accurate, and complete documentation of all tasks within the scope of responsibilities.
  • Maintain close collaboration with other departments to support the effective execution of projects and activities.
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