Software Engineer for Medical Device Development

vor 4 Stunden

Zürich, Zürich, Schweiz Abbott Vollzeit

Software Engineer for Medical Device Development

We are seeking a skilled Software Engineer to join our R&D team in Zurich. As part of our Software Team, you will be responsible for the design and implementation of software for life-sustaining medical devices. Your tasks will include developing embedded software and desktop applications that are part of our product development. In this highly regulated environment, you will be exposed to all aspects of the software life cycle.

Main Responsibilities

  • Design, development, testing, documentation, release, and maintenance of software for medical devices
  • Organize work according to project priorities, deadlines, and deliverables
  • Collaborate on interdisciplinary product development activities during the full life-cycle of class 2 and class 3 medical devices
  • Lead new product development activities, including verification and validation, e.g., test method development
  • Support production activities for the introduction of new products
  • Support regulatory submissions through required documentation
  • (Sub-) Project Management on new product development and sustaining projects

Required Qualifications

  • Master's Degree in Computer Science, Software Engineering, or equivalent (ETH/FH or comparable education)
  • 10+ years of experience in a similar position in the MedTech industry or in another industry that requires functional safety certifications
  • Experience in C/C++ and C#
  • Experience in the complete software life cycle
  • Good understanding of the principles of software architecture and usual design patterns
  • Good collaboration and team playing skills
  • Excellent analytical and creative problem-solving skills
  • Excellent learning skills
  • Flexible developer with accurate working and documentation style
  • Capable of producing quality documentation in English, fulfilling the requirements of the MedTech industry
  • Fluent in German and English

Preferred Qualifications

  • Experience in Requirements Engineering, including product architecture and design transfer of requirements
  • Experience in Design Verification & Validation planning and execution
  • Experience in the development of MedTech software according to IEC 62304
  • Experience in Risk Management and Cybersecurity

We are looking for a passionate individual who masters cross-functional and international collaboration. If you have the skills and experience required for this role, we encourage you to apply. Please submit your application, including a motivation letter, curriculum vitae, letter of recommendation, and diplomas. We look forward to reviewing your application.

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