Staff Supplier Quality Engineer (f/d/m)

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2 Locations
In-Office
Biotech
The Role

Bring more to life.

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

At Beckman Coulter Diagnostics, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

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.

As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory’s role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence.

Learn about the Danaher Business System which makes everything possible.

The Manufacturing Quality Team is seeking a Staff Supplier Quality Engineer to support our Manufacturing Automation Organization in Munich. In this role you will report into the Manager Supplier Quality . In this role, you will manage the quality assurance activities for the manufacturing of our automate instruments at our Munich Location.

Responsibilities:

  • Driving supplier performance improvement through root cause analysis, corrective action and supplier performance reviews;

  • Ensure compliance with the European Medical Device Directive and associated regulations;

  • Liaise with the regional and global Quality & Regulatory Affair organization to support the development of and ensure alignment with BEC global policies and procedures.

  • Establishing and developing commodity requirements.

  • Leads key supplier sourcing and qualifications processes.

Job Requirements:

  • Minimum of 5 years experience in supplier quality area in either medical devices, automotive, aerospace industry or with background in electro-mechanical equipment production

  • Experienced with electronic and mechanical components validation and release.

  • Experienced with quality management methods (i.e. Six Sigma, Problem Solving, Statistical Tools)

  • Knowledge of EU, FDA and related regulations including QSR’s, (FDA 21 CFR 820), ISO 13485, ISO 9001 and the EU IVDD

  • Certified internal auditor ISO 9001or ISO 13485..

  • Experienced in working within multi-functional, multi-regional teams

  • Fluent in German and English languages.

  • Good computer skills which includes Microsoft Applications, Databases and Web-based Tools.

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.

Cepheid Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Cepheid and has not been reviewed or approved by Cepheid.

  • Leave & Time Off Breadth PTO and paid holidays are portrayed as robust, with formal programs and mentions of generous time off and rollover in some cases. This breadth supports a positive view of time-off availability.
  • Healthcare Strength Core medical, dental, and vision coverage is highlighted repeatedly and is viewed as comprehensive for regular full‑time employees. Descriptions such as “good” or “great” benefits reinforce the strength of the health coverage.
  • Retirement Support A 401(k) plan with company matching is consistently included as part of the package. The presence of matching contributions strengthens perceived retirement readiness.

Cepheid Insights

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The Company
HQ: Sunnyvale, CA
4,883 Employees
Year Founded: 1996

What We Do

Cepheid is dedicated to improving healthcare by pioneering molecular diagnostics that combine speed, accuracy, and flexibility. The company's GeneXpert® systems and Xpert® tests automate highly complex and time-consuming manual procedures, providing A Better Way for institutions of any size to perform world-class PCR testing. Cepheid’s broad test portfolio spans respiratory infections, blood virology, women’s and sexual health, TB and emerging infectious diseases, healthcare-associated infectious diseases, oncology and human genetics. The company’s solutions deliver actionable results where they are needed most – from central laboratories and hospitals to near-patient settings. For more information, visit http://www.cepheid.com.

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