Ingénieur.e systèmes / Systems Engineer

Demant

  • Nice, Alpes-Maritimes
  • CDI
  • Temps-plein
  • Il y a 1 mois
-ITSA Medical is a MedTech company located in Sophia Antipolis (Vallauris, France), in the South of France.Do you want to contribute to improving the quality of life of people with hearing loss?If so, we could offer you an exciting career at ITSA Medical in Sophia Antipolis (CDI/ Permanent contract). The bone anchored solutions developed and produced by ITSA Medical are marketed by our sister company Oticon Medical AB.We develop implantable medical devices as well as surgical techniques. The Sophia Antipolis site specializes in the production of transcutaneous implants, product development and sales activities for France.You will be part of the Research & Development team spread over 3 sites, Sophia Antipolis (Vallauris, France), Gothenburg (Sweden) and Copenhagen (Denmark). The R&D team works on the development of future percutaneous and transcutaneous solutions. The position is based in our R&D center located in Sophia Antipolis.Reporting to the Director of Systems Engineering, located at the Danish site, your main responsibility is to identify, in collaboration with project teams, the key aspects of the system architecture of the solutions to be developed. You will play both advisory and execution roles, creating our verification strategy across projects and activities as well as implementing it in key projects.Your Main Tasks
  • Provide input to R&D verification strategy
  • Be responsible for design coordination in development projects
  • Assist in the analysis of requirements and specifications from a verification perspective
  • Participate in product design reviews and team meetings as responsible for project verification
  • Interface with all departments to provide guidance on the use of methodologies, tools, and compliance requirements ensuring consistency with applicable safety and security standards of the product
  • Ensure technical and methodological approach is accurate, adequate, and compliant with quality and regulatory requirements
  • Coordinate, on a need basis, external or internal test warehouses for test executions (example : transport resistance test, labeling compliancy test, aging test, etc.)
Your profile
  • Master's degree in engineering in the field of electronics, software, or other relevant engineering disciplines
  • Minimum of 5 years of verification experience in the medical device industry, or similar experience in another regulated industry with adequate systems engineering practices
  • An inclusive and team-oriented mindset that thrives in a collaborative environment with focus on achieving results in a pragmatic way
  • Energetic, motivated, and proactive person, capable of working in a diverse team in a developing organization
  • Strong interpersonal skills and a supportive attitude to help build a positive team dynamic
  • Excellent communication and influence skills - written and verbal - suitable for a wide range of stakeholders both in projects and management
  • Proficiency in English (reading, writing, speaking)
Working Time and Duration :
  • 39 hours per week
  • Flexible start and departure hours
  • Limited remote work (10 days per month with 40% on site presence per week)

Demant