021 310 07 07 rh@crit.ch

Hardware Engineering Manager (H/F) 100%

In the frame of an «Exclusive Mandate», we would like to present you a new challenge.

Our client, an Innovative Tech company, is currently looking for one Hardware Engineering Manager (Lausanne Area / Fixed position).

In this new challenge, you will be responsible for bringing alignment, ownership, and focus to the hardware engineering team. You lead hardware design of the next-generation robotic surgical solution, fulfilling product and regulatory requirements of a medical device. As part of this scope, you will plan, conduct, and supervise engineering research, design and development.

Responsabilities :

  • Lead, develop, and manage hardware engineering team, provide technical guidance, evaluation, and facilitate career growth
  • Responsible for planning, design, development, prototyping, and testing of complex mechanical or electro-mechanical system
  • Responsible for managing New Product Introduction activities, drive engineering changes, design transfer, and implementation and tracking of changes through change control
  • Project management responsibilities, developing and maintaining project schedules and budget
  • Be accountable for product verification and validation activities in close partnership with contractors and testing laboratories across Europe including electromagnetic compatibility and electrical safety,
  • Manage projects, design, prototype and implement mixed-signal and power electronics, verification & validation,


Profile :

  • Bachelor’s or master’s degree in electrical / electronic engineering, or equivalent
  • 10+ years of experience in the product development role, with at least 3 years in medical device development, or other regulated industries
  • 5+ years of direct people management experience in product development
  • Experience in project, program, and portfolio management in a complex new product development environment
  • Wide-ranging know-how of electronics: mixed signal, power electronics printed circuit boards, cabling, and system level architecture/integration (HW/ME/SW).
  • At ease organizing and executing requirements-driven development and verification activities.
  • Capable of scoping and executing risk management activities with the team (e.g. FMEAs, or similar)
  • Experience working within a quality management system (e.g. ISO 9001, ISO 13485 or similar)
  • At ease working with engineering disciplines such as: mechanics and software, and other company functions including QA, Regulatory Affairs, Operations and Supply Chain
  • Professional oral and written French and English and able to travel (10%) within Europe.
  • Bonus Points
  • Experience with medical industry regulations such as IEC60601
  • Experience in the Life Sciences or a related industry

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

TYPE DE TRAVAIL: Engineering Medical Device
TYPE DE POSTE: Plein temps Poste fixe

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