Be part of something altogether life-changingWorking 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.

We're looking for our next Validation and Verification Engineer t o join our Verification and Streaming team within the Customized Bioprocess Solutions (CBS) organization at Cytiva's site in Uppsala. As Validation and Verification Engineer at Cytiva, you will be responsible for planning and execution of functional test of our custom hardware products. This position is located in Uppsala, Sweden and will be a hybrid role.

What you'll do:

• Plan and execute functional test of custom hardware products.

• Review and reject/approve test results and to check and approve/reject other test engineers test protocols and documentation.

• Develop and write procedures for functional testing, perform troubleshooting and suggest corrective actions.

• Educate suppliers, customers and service engineers as well as participate in technical discussions and customers FAT.

The essential requirements of the job include:

• BSc degree or equivalent, preferably within electrical engineering. Alternatively, you have a comparable level of work life experience.

• High technical competence and deep understanding of control software.

• Fluency in English, both written and spoken.

It would be a plus if you also possess previous experience in:

• Knowledge of Cytiva Bioprocess products.

• Experience from testing/verification of operating systems.

• Experience from GMP and/or other regulated business areas.

• Fluency in Swedish, both written and spoken.

  To be successful in this role, we believe that you are a structured, analytical person with a excellent team-working skills. We believe that you are an energized and results-oriented self-starter.

Interview and selection will happen continuously and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Robert Gardelius, robert.gardelius @cytiva.com.

At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.

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