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Danaher Corporation Senior QA Engineer in Umea, Sweden

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 role as Senior QA Eng ASME (American Society of Mechanical Engineer) gives a unique opportunity to work with the entire product production lifecycle. The work will be focused on Cytiva Umeå production and will be an on-site role. The main responsibility of the role is linked to the ASME projects but as a team member in the Quality department you will also be working in other quality related areas together with colleagues.

In this role, you will have the opportunity to:

  • Act as support for the factory around the ASME standard and be responsible for the contact with external inspector.

  • Plan and lead audits related to the ASME manual.

  • Act on findings from audits, conduct investigations and improvement work.

  • Lead and coach others in their work. Coordinate site activities related to manufacturing according to the pressure vessel standard ASME.

  • Monitor ASME standard and implement changes into local procedures.

  • Support local business functions to secure quality and regulatory compliance in accordance with documented procedures.

  • Learn, grow and work in multiple other QA related processes.

The essential requirements of the job include:

  • Bachelor’s degree (or working experience in Quality Assurance or 4 years working experience in hardware/pharmaceutical industry.)

  • Demonstrated understanding of manufacturing processes, product development lifecycles, design change and document change control.

  • Ability to coordinate, handle & prioritize tasks effectively.

  • Excellent oral communication and reporting skills in Swedish and English.

  • Excellent business correspondence and procedure-writing skills in Swedish and English.

  • Turn plan into actions with clear steps of assigned responsibilities and make accurate decisions using the best information available.

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

  • Project management

  • Knowledge of the ASME standard

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.

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.

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