Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Software Engineer to work with our expert R&D team of 22 associates across the world. Do you have a passion for R&D? Then we would love to hear from you.
What you’ll do
Be an active contributor in software development team responsible for designing new features and supporting / improving legacy products (product care)
Collaborate on the project with other team members in several locations, including third party companies.
Participate in writing SW project specifications, and possible help on verification and validation activities with focus on quality, compliance and execution rigor.
Participate in documenting the project file including user requirements, project planning, design input and output and set up and maintain the technical dossier for regulatory compliance.
Ensure compliance with ISO13485 or ISO9001 standards and other QMS requirements.
Who you are
Master’s degree or equivalent experience in software engineering
3 to 7 years of successful experience in R&D and project execution
Excellent knowledge in C#, good understanding of C/C++
Experiences in development under .NET framework is a must
Experiences with embedded systems (software & hardware) is desired, firmware development a plus
Experiences with software testing is desired (unit tests, integration test, BDD, TDD)
Experiences of work linked to cybersecurity and data privacy is a plus
Knowledge or experiences of agile development best practices is a must
At ease in analysis and review of debugging and crash-log data
At ease with requirements / features specification
Ability to navigate in ambiguous situation and resolve issues on-time
Demonstrated experience in launching SW products following a development life cycle under a quality management system
Experience in large multidisciplinary projects with multiple stakeholders involved is a plus
Experiences of working with laboratory / medical devices and/or relevant regulations (ISO 9001, ISO 13485, cGMP, ISO 62304) is a plus
Customer-oriented mindset, autonomous at work, creative and initiatives welcomed
Demonstrated ability to clearly communicate (oral, written) across global, cross-cultural, cross-functional teams and stakeholders
Fluent in English, a second language is a plus
Who we are Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.