Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
What you’ll do
Execute software verification activities and be responsible for the quality, test plans and testing methodology for the Software
Analyze design requirements to develop and contribute to the implementation of Test Automation Architecture and framework
Perform defect investigation studies and White, Grey, and Black Box testing
Provide consolidated status reports for defects and test case execution progress with respect to plan
Be an active contributor in software development team responsible for designing new features and supporting/improving legacy products
Support maintaining build server and implement continuous integration (automatic quality assurance processes)
Ensure compliance with ISO13485 or ISO9001 standards and other QMS requirements.
Who you are
University degree or equivalent experience in software compliance assurance engineering
Knowledge of C++\C# and scripting or other programming language
Some experience with software requirements, in analysis investigation and review of debugging and crash-log data, and with automated functional, stress, and performance testing scripts & tools
Interested in developing multi-layers software following Agile development best practices and development life cycle running on laboratory devices, or IVD, or medical devices or manufacturing equipment running in a GMP environment.
Interested in verification of complex, multi-threaded, and multi-component software and in gaining experience with Behavior-driven development and Test-driven development
Ability to navigate in ambiguous situation and resolve issues on-time
Ability to clearly communicate (oral, written) across global, cross-cultural, cross-functional teams and stakeholders
Interested in gaining knowledge and practical experience of relevant regulations (ISO 9001, ISO 13485, IEC 62304, cGMP, GAMP), specifically for the US and European market
Fluent in English, a second language is a plus
Customer-oriented mindset, autonomous at work, creative and initiatives welcomed
When you join us, you’ll also be joining Danaher’s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.
Danaher is committed to a diverse and inclusive culture where everyone feels they belong and all voices are heard. We believe in our associates and the unique perspectives they bring to every challenge, which is why we’ll empower you to push the boundaries of what’s possible.
If you’ve ever wondered what’s within you, there’s no better time to find out.