Auf einen Blick
- Aufgaben: Lead quality and regulatory improvements in a fast-paced environment.
- Arbeitgeber: Beckman Coulter Diagnostics is dedicated to advancing healthcare through innovative diagnostic tools.
- Mitarbeitervorteile: Enjoy a supportive culture, career growth opportunities, and collaboration with global teams.
- Warum dieser Job: Make a real impact on patient lives while working in a diverse and inclusive team.
- Gewünschte Qualifikationen: Master's degree in a scientific field and experience in medical device quality or regulatory affairs required.
- Andere Informationen: Position based in Munich with minimal travel; join us to shape the future of healthcare.
Das voraussichtliche Gehalt liegt zwischen 54000 - 84000 € pro Jahr.
**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 (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: * 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: * Masters degree in a scientific field with years of proven experience required. * Experience in quality andor 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. **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](http: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.
Beckman Coulter Diagnostics | Quality & Regulatory Change Manager (m/f/d) (Apply in minutes) Arbeitgeber: Beckman Coulter Diagnostics

Kontaktperson:
Beckman Coulter Diagnostics HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Beckman Coulter Diagnostics | Quality & Regulatory Change Manager (m/f/d) (Apply in minutes)
✨Tip Number 1
Familiarize yourself with the Danaher Business System (DBS) and its principles. Understanding how DBS drives quality and regulatory processes will help you demonstrate your alignment with Beckman Coulter's goals during the interview.
✨Tip Number 2
Highlight your experience in quality and regulatory affairs within the medical device sector. Be prepared to discuss specific projects where you implemented process improvements or navigated complex regulatory challenges.
✨Tip Number 3
Showcase your leadership skills by providing examples of how you've successfully led cross-functional teams. Emphasize your ability to build trust and credibility with stakeholders, as this is crucial for the role.
✨Tip Number 4
Prepare to discuss your problem-solving abilities and innovative solutions you've developed in past roles. This will demonstrate your capability to drive improvement projects effectively within the WITS QRA organization.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Beckman Coulter Diagnostics | Quality & Regulatory Change Manager (m/f/d) (Apply in minutes)
Tipps für deine Bewerbung 🫡
Understand the Role: Take the time to thoroughly read the job description for the Quality & Regulatory Change Manager position. Understand the key responsibilities and requirements, especially the emphasis on quality and regulatory affairs in a medical device environment.
Highlight Relevant Experience: In your application, make sure to highlight your experience in quality and regulatory affairs, particularly in the medical device sector. Use specific examples that demonstrate your expertise and how it aligns with the role's requirements.
Showcase Your Skills: Emphasize your skills in continuous improvement, Lean methodologies, and your ability to lead cross-functional teams. Provide concrete examples of how you've successfully implemented process improvements in previous roles.
Tailor Your Application: Customize your CV and cover letter to reflect the language and values mentioned in the job description. Show your enthusiasm for working at Beckman Coulter Diagnostics and how you can contribute to their mission of advancing healthcare.
Wie du dich auf ein Vorstellungsgespräch bei Beckman Coulter Diagnostics vorbereitest
✨Understand the Company Culture
Beckman Coulter Diagnostics values diversity and collaboration. Make sure to express how your background and experiences align with their commitment to a supportive and inclusive workplace.
✨Highlight Relevant Experience
Prepare to discuss your experience in quality and regulatory affairs, especially in the medical device sector. Be ready to provide specific examples of how you've successfully navigated complex regulatory environments.
✨Demonstrate Problem-Solving Skills
Since the role involves driving process improvement projects, be prepared to share instances where you've identified innovative solutions or led teams to solve complex problems.
✨Showcase Communication Abilities
Effective communication is key in this role. Practice articulating difficult concepts clearly and concisely, and think of examples where you've successfully negotiated or collaborated with cross-functional teams.