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

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

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

Beckman CoulterDiagnostics is proud to work alongside a community of six fellowDiagnostics Companies at Danaher. Together, we’re working at thepace of change to improve patient lives with diagnostic tools thataddress the world’s biggest healthchallenges.

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

At Beckman Coulter, ourvision is to relentlessly reimagine healthcare, one diagnosis at atime.

Do you want to thrive ina multifunctional, fast paced and central role and work in closecollaboration with the different DBS representatives for QRC(Quality, Regulatory and Clinical Affairs) and the relevantBUs?

In thisrole, you will have the opportunityto :

Establishand maintain DBS funnel for WITSQRA.

Support and helpdevelop DBS capabilities of the WITS QRAorganization.

Facilitate DBSevents for WITSQRA.

Interact andcollaborate with BEC globalcounterparts.

In addition tothe responsibilities above the WITS QRA DBS lead will drivespecific process improvementprojects.

Theessential requirements of the jobinclude :

Master'sdegree in a scientific field with years of proven experiencerequired.

Experience inquality and / or regulatory affairs in a medical deviceenvironment.

Excellentknowledge of medical device quality system regulations andstandards.

DBS, Lean orcontinuous improvementexperience.

Fluent inEnglish, German aplus

Itwould be an advantage if you also have previous experience in thefollowingareas :

Excellentorganisational and cross-functional leadershipskills.

Abilityto quickly establish credibility and trustworthiness with keypartners, ability to buildfollowership.

Abilityto communicate difficult concepts and negotiate withothers.

Abilityto lead others to solve complexproblems.

Abilityto identify innovativesolutions.

Travelrequirements :

Position based inMunich, travel needs up to10%.

Joinour winning team today. Together, we’ll accelerate the real-lifeimpact of tomorrow’s science and technology. We partner withcustomers across the globe to help them solve their most complexchallenges, architecting solutions that bring the power of scienceto life.

For moreinformation, visit www.danaher.com .

At Danaher, wevalue diversity and the existence of similarities and differences,both visible and not, found in our workforce, workplace andthroughout the markets we serve. Our associates, customers andshareholders contribute unique and different perspectives as aresult of these diverseattributes.