Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

Together with Danaher’s 15+ other operating companies, we unlock the transformative potential of cutting-edge science and technology to improve billions of lives every day.

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

HemoCue is a leading provider of point-of-care diagnostic solutions, enabling healthcare practitioners across clinical settings and geographies to improve patient outcomes and clinical workflows. For more than four decades we’ve been advancing what’s possible at the point of care. HemoCue offers point-of-care testing for hemoglobin, glucose and HbA1c as well as total and differential white blood cell count.

The Validation engineer for HemoCue is responsible for process validation and calibration in our production.

This position is part of the Integrated Engineering within operations located in Ängelholm and will be on-site. At HemoCue, our purpose is clear: advancing care, test by test, everywhere. Care is the bedrock upon which we stand. It’s manifested in our devices, our people and how we interact with the world.

You will be a part of the Integrated Engineering Operations and report to the Director Integrated Engineering responsible for maintaining production capacity. If you thrive in a senior validation role and want to work to build a world-class organization supporting medtech production, read on.

In this role, you will have the opportunity to:

• Lead and ensure process validations, including validation of methods (instrumentation) and software systems (both instrument and production environments).
• Plan and perform measurement system analyses
• Guide colleagues on validation matters
• Take the lead in executing and documenting validation activities
• Assist during audits regarding process validation-related questions
• Design and conduct experiments to improve manufacturing processes
• Use statistical methods as a basis for decision-making

The essential requirements of the job include:

• University degree in engineering or equivalent, with experience in similar positions
• Knowledge of FDA, CFR Part 820, and ISO 13485
• Broad validation experience, minimum 3 years
• Ability to apply statistical methods to practical problems

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

• Measurement technology
• Vision system

Union contacts: Henrik Pommer, Unionen, +46 431 481 244 or Katarina Cooper, Akademikerföreningen, +46 431 481 302

Join a winning team today. Together, we’ll 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.

For more information, visit www.danaher.com.

Join our winning team today. Together, we’ll 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.

For more information, visit www.danaher.com.