021 310 07 07 rh@crit.ch

Head of Software 100% (H/F)

We would like to present you a new challenge. Our client, an Innovative Med Tech company, is currently looking for Head of Software (Nyon Area / Fixed position).

Responsabilities :

You ‘ll be responsible for complete software development life cycle including maintenance activities related to class IIb surgical robots and accessories – ranging from low-level firmware and applicative software up to data analytics in the cloud

Profile :

  • Strategize and manage software development and verification teams and resources, covering people development and capacity management.
  • Drive risk management activities for all software development and participate to overall project risk management activities with team.
  • Drive process and tools improvements supporting complete software development life cycle.
  • Account for delivering software product releases in a timely manner according to the Company’s product roadmap.
  • Contribute to road-mapping activities and to project and product definitions.
  • Ensure compliance with relevant norms (e.g. ISO 13485, ISO 14971, IEC 62304, IEC 60601-1, IEC 80601-2-77) and regulations (e.g. MDD and MDR for Europe).
  • Establish and maintain appropriate documents and records in compliance with Company’s Quality Management System

 

Please send us your CV, copies of diplomas and a cover letter.

  • Master level with degree or similar in a relevant discipline, such as Computer Science, Electronics and Electrical Engineering, Mechatronics (or similar)
  • English Fluent. French &/or German a plus
  • Strong leadership & strategizing skills, successful experience with managing and growing medium-sized teams
  • At least 3+ years in a leadership role in software development & verification in the Medical Device sphere (class IIa / IIb / III) is mandatory.
  • Experience in the development and verification of embedded real-time software,
  • Deep knowledge of software engineering, both process and tools (incl. continuous integration)
  • Experience performing software risk management for Class IIa (or higher) medical devices and development under medical device regulations (IEC 62304) and working within an ISO 13485 certified QMS
  • Solid understanding of structured product development (requirements-driven engineering, architecture modeling, detailed design, SW FMEA, formal verification, release processes, etc.)
SECTEUR D'ACTIVITE: Industrie & Production
TYPE DE POSTE: Plein temps Poste fixe
LIEU DE TRAVAIL: Canton de Vaud
AGENCE: Crit Expert

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