Be part of something altogether life-changing
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
Be part of R&D Applications team and support developers with activities linked to V&V in context of new products development and change controls
Design verification plan and test cases based on sub-system functional requirements and user stories acceptance criteria
Execute application workflow tests and functional performance tests with focus on quality, compliance and execution rigor
Be responsible for the testing documentation and methodology
Perform defect investigation studies and test case execution progress with respect to plan
Contribute to the Applications development team by maintaining and enhancing testing tools and framework
Actively participate in the Applications development team group life, i.e. attending to meetings and workshops, proposing improvements, etc.
Ensure compliance with ISO13485 or ISO9001 standards and other QMS requirements.
Who you are
University degree (Master) in Computer Sciences, Computer Engineering, Biomedical Engineering or equivalent
1-3 years’ work experience in R&D department related to above fields
Knowledge and previous experience in developing in any programming language is a must
Prior experience in participating in software development by using development methodologies and source code management (e.g. Agile, Waterfall, GitHub)
Knowledge and previous experience in any markup language (e.g. XML, TeX, HTML) is preferrable
Knowledge of statistical software analysis (e.g. MATLAB, Minitab) is preferrable
You have some experience with software requirements and integration testing, debugging, machine log analysis, data analysis with scripts and tools
You are interested in contributing in development lifecycle of Applications 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.
You have strong analytical thinking, you pay attention to details and you have a structured approach in your daily work
You have a strong documentation bias and good oral and written communication skills
Interested in gaining knowledge and practical experience of relevant regulations (ISO 9001, ISO 13485, cGMP), 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.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
If you’ve ever wondered what’s within you, there’s no better time to find out.