Continuous Improvement Lead (DBS Lead) Quality & Regulatory (m/f/d)

Wondering what’s within Beckman Coulter Diagnostics? Take a closer look.

At first glance, you’ll see that for more than 80 years we’ve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We’re building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you’ll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful.

Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges.

The QRA DBS (Danaher Business System) Lead (m/f/d) will be Working within the WITS (Workflow and IT Solutions) Q&RA (Quality and Regulatory Affairs) organization to drive improvement within QRA processes for the two business units: Automation (AUT) and Clinical Informatics (CIT). This position is part of the Quality Team located in Munich and will be on-site and will support sites in EU and India. The QRA DBS Lead reports to VP Quality and Regulatory Affairs.

At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time.

Do you want to thrive in a multifunctional, fast paced and central role and work in close collaboration with the different DBS representatives for QRC (Quality, Regulatory and Clinical Affairs) and the relevant BUs?

In this role, you will have the opportunity to:

Establish and maintain DBS funnel for WITS QRA.

Support and help develop DBS capabilities of the WITS QRA organization.

Facilitate DBS events for WITS QRA.

Interact and collaborate with BEC global counterparts.

In addition to the responsibilities above the WITS QRA DBS lead will drive specific process improvement projects.

The essential requirements of the job include:

Master's degree in a scientific field with years of proven experience required.

Experience in quality and/or regulatory affairs in a medical device environment.

Excellent knowledge of medical device quality system regulations and standards.

DBS, Lean or continuous improvement experience.

Fluent in English, German a plus

It would be an advantage if you also have previous experience in the following areas:

Excellent organisational and cross-functional leadership skills.

Ability to quickly establish credibility and trustworthiness with key partners, ability to build followership.

Ability to communicate difficult concepts and negotiate with others.

Ability to lead others to solve complex problems.

Ability to identify innovative solutions.

• Position based in Munich, travel needs up to 10%.

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 .

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.