FR - Nice

Verification and validation engineer F/H


FR - Nice
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Verification and validation engineer F/H

Verification and validation engineer F/H 
Do you want to contribute to the improvement of the life experience for people with a hearing disability?  
Then we might have an exciting career for you as Verification and validation engineer at Oticon Medical in Vallauris (France).

Oticon Medical is committed to improve the quality of life of profoundly deaf patients. For that, we develop implantable medical devices and surgical techniques to restore profound hearing loss. As a member of one of the world’s largest groups of hearing health care companies, we share a close link with Oticon and direct access to the latest advancements in hearing research and technologies. Our competencies span more than a century of innovations in sound processing and decades of pioneering experience in hearing implant technology. 
Key responsibilities  
In your job you will be part of Oticon Medical / Neurelec R&D in Vallauris France, situated on the French Rivera. You will be working in a multi-disciplinary and competent product development team together with electro-acoustic engineers, software designers, audiologists and embedded system designers.  The Verification and validation engineer is responsible for regulatory compliance testing of the medical device. Your main responsibilities are:  
- Define test plans to verify product compliance with applicable regulations and standards;
- Define test benches;
- Execute tests and analyze results;
- Elaborate test report;
- Ensure regulatory compliance.  

You will have as well the opportunity to involve yourself in product usability evaluation by: 
- Define test plan for formative evaluation;
- Contribute identifying usability specifications, user errors and usability risks;
- Elaborate summative evaluation, test protocol, perform the usability tests and write report; - Evaluate tests results and usability risks. 

Experience in validating medical devices 
You have a Bachelor and/or a master’s degree in engineering and you have least 3 years of experience in the validation of medical devices.  This would be a plus if you have experience in AIMD and/or in the usability process.  
As a person you have good communication skills and are a team player by heart. You are motivated by the quality of product, with a clear focus on customer needs, and by working in cross-professional development teams. You are dedicated about your work, are self-managed and constantly focused on your goals.  We expect you to be fluent in English. 
Our commitment to making a difference 
Together with skilled colleagues, you are part of a dynamic environment based on trust and openness, and you will experience a strong passion for our patients. We are a growing international company where everybody supports the business by making sure we successfully bring the best experience with our products to our users. You will be working in a bright and open workplace, where a flexible working environment, knowledge sharing and professional respect makes it meaningful to go to work. 
Want to join the team?  
Then send your application and CV no later than 31th March.  To learn more about the job, please contact Human Resources team,  
We look forward to hearing from you.  
About Oticon Medical 
Oticon Medical is part of the William Demant Holding Group, a Danish owned company with more than 12.000 employees worldwide and revenues totaling DKK 12 billion. The group's products are sold in more than 100 countries, and 98% of Group revenues are generated outside Denmark. Oticon, the largest company of the group, has more than 100 years of experience and today is one of the world's leaders in the industry. We have secured this position by being experimental, creative and effective in finding new solutions. And we work together towards a common goal: to provide people who wish to improve their hearing with the best solutions.