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Validation Engineer at Cytiva in Uppsala

Cytiva Sweden AB

Uppsala län, Uppsala

Previous experience is desired

28 days left
to apply for the job

Be a part of something truly life-changing

Working at Cytiva within the Life Science industry means being at the forefront of developing new solutions to improve people's health. Our customers' operations are life-critical and include everything from fundamental biological research to the development of innovative vaccines, new drugs, and cell and gene therapies.

At Cytiva, you will constantly be able to develop yourself and us - by working on challenges that truly matter alongside people who care about each other, our customers, and their patients. With employees in 40 countries, Cytiva is a place where every day is an opportunity to learn so you can kickstart your career and enhance your skills in the long term.

We at Cytiva are proud to work together with a group of nine other Danaher Life Sciences companies. Together, we are pioneers in science and medicine, developing products that help researchers in the fight to save lives.

We are now looking for a Validation Engineer for the Manufacturing Engineering department, which is part of our large-scale chemical production operations in Uppsala. The validation group, which is a section within the Manufacturing Engineering department, currently consists of 16 validation engineers working towards our production during renovations, new installations, process and control system changes.

The production in Uppsala includes several different manufacturing departments, and as a validation engineer with us, you will have the opportunity for varied tasks and to grow in your professional role.

Your responsibilities:

  • Plan, design, and execute validations.
  • Work on development and improvements.
  • Review/assess specifications, risk assessments, and change requests.
  • Present validation documentation during audits.

The main requirements for the position are:

  • Technical/Natural Science university degree, preferably a master's degree or equivalent.
  • Experience from the biotechnology, pharmaceutical, or process industry.
  • Very good knowledge of Swedish and English, both spoken and written.
  • Experience in project management.

It is also advantageous if you have previous experience in:

  • Good knowledge of validation work.
  • Experience in validation within computerized/automation systems in production, water validation, cleaning validation, process validation, as well as installation and functional qualification.

For the role of validation engineer, we are looking for someone who is driven and responsible in their work. As a person, you have a good ability to analyze problems and quickly manage their solutions. You are flexible, easy to collaborate with, and coordinate projects. You have good planning skills, can work independently, and make decisions. You are service-oriented with great integrity. The work also requires that you are structured and skilled at expressing yourself briefly and concisely in writing to accurately, clearly, and comprehensively describe the purpose and results of validations.

Selection and interviews are ongoing, and the position may be filled before the application deadline. For questions regarding this position, please contact the recruiting manager Therese Håfström at [email protected]. We warmly welcome your application!

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