Design Validation Lead - Medical Devices - Magog, Canada

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.

At Arjo, we know what drives us! We go above and beyond to help people with limited mobility. We seize every opportunity to work and grow as a team and are proud to share our knowledge and experience. Does this resonate with you too? 

You could have the opportunity to start a challenging and rewarding career with a healthcare company that promotes mobility for people with reduced mobility. This is where the future of healthcare is being designed.

At Arjo, we develop medical products that improve patient mobility and optimize the work of healthcare professionals. Our Magog site plays a key role in the design and manufacture of standing and rail lifts for hospitals and long-term care facilities.

As a Validation engineer at Arjo, you will contribute to concrete, challenging, and meaningful projects in a collaborative environment where technical expertise is valued. Join a passionate team where innovation, quality, and human impact are at the heart of every decision.

Why choose Arjo :

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  Flexible working hours and the option to work remotely, supporting a healthy work–life balance;
  
  


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  A friendly and inclusive work environment, built on strong human values, collaboration and mutual respect;
  
  


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  Comprehensive group insurance (dental, vision and medical), with 75% of the premium covered by the employer;
  
  


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  A retirement savings plan (RRSP) with an employer contribution of up to 4.2%;
  
  


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  Three weeks of annual leave from day one, in addition to floating days off and paid leave during the Christmas holiday period;
  
  


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  Reimbursement of expenses related to physical activity;
  
  


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  Team-building activities that foster collaboration and enjoyment at work;
  
  


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  Opportunities to travel abroad depending on project requirements;
  
  


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  On-site electric vehicle charging station;
  
  


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  An exceptional natural setting, ideal for outdoor enthusiasts.
  
  

Responsibilities and duties :

• Participate in the development of new patient lifts and mobility aids according to the Product Development Process (PDP) and regulatory requirements;


• Collaborate with the product development team to understand product usage scenarios, usage environment and user profile;


• Ensure that the suitability and human factors aspects of risk management are carried out, and comply with product development guidelines and regulatory requirements (e.g. IEC 62366, IEC 60601-6, etc.) in each of the projects;


• Carry out, in collaboration with the project teams, the drafting of documentation related to usability;


• Work in collaboration with the Design Assurance Manager to determine evaluation and validation requirements;


• Carry out, in collaboration with the product development team, product evaluations and validation, which may include organizing activities with users, carrying out these activities, writing protocols and final reports;


• Analyze results, and apply basic statistics to make informed decisions on the suitability of products;

Requirements : 

• College or University degree in healthcare combined with 1 to 5 years of experience including use of Patient Handling Product, or


• University degree in mechanical engineering, Industrial Design or other relevant field, combined with 1 to 5 years of experience in medical product development; 


• Strong skills in work organization, planning, and priority management;


• Good analytical skills and ability to work well in a team;


• Knowledge of regulations governing medical product development;


• Rigorous and autonomous. 

Language Requirements : 
This position requires an excellent command of French (level 5/5) and a strong proficiency in English (level 4/5). These skills are critical for effective collaboration with development teams and partners across various Arjo sites worldwide. English communication is essential for project coordination, adherence to international standards, and consultation of technical documentation, which is often available exclusively in English. Meeting these requirements ensures successful task execution in a global environment.

About Arjo

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