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.
TheQRA DBS (Danaher Business System) Lead (mfd) 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:
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Establish and maintain DBS funnel for WITS QRA.
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Support and help develop DBS capabilities of the WITS QRA organization.
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Facilitate DBS events for WITS QRA.
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Interact and collaborate with BEC global counterparts.
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In addition to the responsibilities above the WITS QRA DBS lead will drive specific process improvement projects.
The essential requirements of the job include:
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Masters degree in a scientific field with years of proven experience required.
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Experience in quality andor regulatory affairs in a medical device environment.
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Excellent knowledge of medical device quality system regulations and standards.
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DBS, Lean or continuous improvement experience.
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Fluent in English, German a plus
**It would be an advantage if you also have previous experience in the
following areas:**
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Excellent organisational and cross-functional leadership skills.
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Ability to quickly establish credibility and trustworthiness with key partners, ability to build followership.
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Ability to communicate difficult concepts and negotiate with others.
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Ability to lead others to solve complex problems.
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Ability to identify innovative solutions.
Travel requirements:
- 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.
