Design Assurance Specialist - Magog, Canada
Arjo
Date: 1 hour 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 Design Assurance Specialist, you will be responsible for:
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 Design Assurance Specialist, you will be responsible for:
- Supporting the Product Development and Engineering (PD&E) team to ensure that design requirements (design inputs and user needs) comply with internal product development guidelines as well as applicable regulatory standards and requirements.
- Ensuring the rigorous application of risk management principles across all projects, including the analysis of historical data related to similar products (complaints, CAPAs, service parts, etc.).
- Reviewing and approving product-related documentation to ensure that design dossiers comply with current regulatory requirements.
- Coordinating engineering actions arising from the quality system (nonconformities, audit observations, etc.) and ensuring proper follow-up.
- Ensuring the validation of software tools used by the department (Excel spreadsheets, test benches, etc.).
- Maintaining close collaboration with other departments to support the efficient execution of projects and activities.
- Bachelor’s degree in engineering or science, combined with at least three (3) years of relevant experience in a regulated environment, or any equivalent combination of education and experience.
- Proficiency in English at an intermediate to advanced level (4/5).
- Full professional proficiency in French (5/5).
- Knowledge of quality systems.
- 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.
- Knowledge of regulations related to medical product development (an asset).
- Experience in the medical field or in a highly regulated industry (an asset).
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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