Vacant job

Be a Part of Something Truly Life-Changing

Working at Cytiva in the Life Science industry means being at the forefront of developing new solutions to improve human health. Our customers' activities are life-critical and include everything from basic 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 together with 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 advance your career and improve 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 Senior QA Engineer - Projects for the QA Projects section at Cytiva's QA department in Uppsala. As a Senior QA Engineer, you will represent QA in R&D and site projects with a special focus on validation activities. In this role, you will work cross-functionally with colleagues from production, R&D, and PMO, among others. The position is an on-site role based in Uppsala.

In this role, you will have the opportunity to:

• Represent QA in cross-functional projects such as new product and equipment projects.
• Contribute to ensuring that validation activities are completed within set timelines, in close collaboration with other functions.
• Represent QA in cross-functional risk analyses.
• Review and approve risk analyses, validation documentation, and deviations.
• Actively participate in and drive change and continuous improvements within projects and processes.
• Ensure compliance with our quality management system (QMS) in close collaboration with the rest of the organization.

The basic requirements for the position are:

• University degree in chemistry, pharmacy, or equivalent.
• Several years of experience in similar QA roles within regulated Life Sciences operations (e.g., ISO 9001, ISO 13485, and/or GMP).
• Experience representing QA in projects.
• Good knowledge of validation and qualification activities in automation, process equipment, and CSV.
• Experience in driving and/or representing QA in risk analyses.
• Experience in driving and/or representing QA in deviation investigations.
• You communicate fluently in Swedish and English, both verbally and in writing.

It is also advantageous if you have:

• Good knowledge of risk analysis methodologies.
• Experience in complex QA projects and activities.

Selection and interviews are ongoing, and the position may be filled before the application deadline. For questions related to the position, please contact recruiting manager Erika Lodén, Section Manager QA - Projects, [email protected].