Validation and verification engineer

Be part of something altogether life-changing!
Working at Cytiva 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.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Validation and Verification Engineer is responsible for performing verification on time with guidance from senior engineers, planners and project managers according to customer demand.
The Verification section is responsible for planning and execution of functional tests on Bioprocess equipment developed by Custom Engineering.
This position is part of the Verification section in Uppsala and will be an on-site role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Verification:
Functional testing of Custom engineering equipment.
Support projects to ensure quality and timely delivery of plans and results through daily management.
Support planning and development activities for coming projects.
Participate in customer FATs.
Participate in troubleshooting and suggestion of corrective actions for products, test methods, procedures etc.
Quality inspections of products at sub supplier or at Custom engineering.

Documentation:
Deliver verification documentation and test results.
Participate and or propose development of wow/procedures/methods.

Service/Expertise:
Support training of new resources, secure that GDP and other regulatory requirements are understood and fulfilled.
Support maintenance & development of test facility and test equipment.
Perform installations/troubleshooting at customer site.
Support service with maintenance and repair of customized equipment.
Participate in resolution of case management, CAPA, risk analysis.

The essential requirements of the job include:
Bsc. in mechanical or electrical engineering or similar knowledge from working experience.
GMP knowledge or experience from other regulated business areas.
Experience from testing/verification of operating systems.
Knowledge from Cytiva Bioprocess products.
Fluency in English, both written and spoken.

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