Technical Documentation Specialist - Magog, Canada - #224934
Arjo
Date: 2 weeks ago
City: Magog, QC
Contract type: Full time
Empowering careers at ARJO
At Arjo, we know what moves us. We go above and beyond for people facing mobility challenges. We take every opportunity to work and grow as one team and take pride in sharing our knowledge and experience. Does that sound like something that moves you too?
This could be your opportunity to begin a challenging and rewarding career in a healthcare company that empowers movement for people with mobility challenges.
As a Technical Documentation Specialist, you will be responsible for the following:
At Arjo, we believe that empowering movement within healthcare environments is essential to quality care. Our products and solutions are designed to promote a safe and dignified experience through patient handling, medical beds, personal hygiene, disinfection, diagnostics, and the prevention of pressure injuries and venous thromboembolism. With over 6500 people worldwide and 65 years caring for patients and healthcare professionals, we are committed to driving healthier outcomes for people facing mobility challenges.
For more information about Arjo visit www.arjo.com
At Arjo, we know what moves us. We go above and beyond for people facing mobility challenges. We take every opportunity to work and grow as one team and take pride in sharing our knowledge and experience. Does that sound like something that moves you too?
This could be your opportunity to begin a challenging and rewarding career in a healthcare company that empowers movement for people with mobility challenges.
As a Technical Documentation Specialist, you will be responsible for the following:
- 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.
- 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).
- Experience in the medical field or in a highly regulated industry (an asset).
- 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.
At Arjo, we believe that empowering movement within healthcare environments is essential to quality care. Our products and solutions are designed to promote a safe and dignified experience through patient handling, medical beds, personal hygiene, disinfection, diagnostics, and the prevention of pressure injuries and venous thromboembolism. With over 6500 people worldwide and 65 years caring for patients and healthcare professionals, we are committed to driving healthier outcomes for people facing mobility challenges.
For more information about Arjo visit www.arjo.com
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