CAREERS

Your responsibilities

• Providing software system life cycle expertise within broader cross‐functional medical device development teams

• Supporting the standardization of the entire medical device software lifecycle management process to comply with IEC 62304 and other relevant standards and regulations

• Leading customer projects and supporting project teams with writing, reviewing and submitting technical documentation for medical device software

• Providing technical expertise on cybersecurity, data protection and AI/ML related topics in the healthcare sector

Your profile

• Strong background in computer science, agile software development, CI/CD, DevOps

• Excellent understanding of software lifecycle management, software risk management, verification and validation strategies

• 3+ years of experience with the development of safety critical software, ideally in the medical device or pharmaceutical industry

• Excellent technical writing skills

• Autonomous and independent working style

• Ability to quickly understand our customer’s needs and provide specific solutions to their problems

• Fluent in English, German and/or French would be an asset

Who we are

QUAREGIA supports small to global healthcare companies in bringing their products to market. We focus on medical device software and health apps and provide customer specific solutions to fulfill regulatory requirements. If you are fascinated by pragmatic solutions bridging agile software development and regulations, this might be your next career step.

What we offer

• An innovative work environment and challenging projects in a growing field

• A flexible working model (home office, flexible working hours)

• Attractive compensation model

Please send your application with a letter of application by email to sabine.nieba@quaregia.com