Beckman Coulter Diagnostics

Manufacturing Quality Engineer (f/m/d)

Stellenbeschreibung:

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. By harnessing Danaher’s system of continuous improvement, you help turn ideas into impact—innovating at the speed of life.

Manufacturing Quality Engineer (f/m/d)

In This Role, You Will Have The Opportunity To

  • Lead non‑conformance investigation for internal and customer claims in the scope of manufacturing.
  • Define programs for manufacturing quality improvement.
  • Monitor and improve quality manufacturing KPI’s.
  • Liaise with supplier quality team on quality topics, containment activities, corrective actions at supplier.
  • Execute and participate in internal audits.
  • Lead Material Review Board meetings.
  • Create and update manufacturing‑related quality system documents.
  • Liaise with Engineering teams on validation requirements for new and current products and processes as well as with the regional and global Q&RA organization to support the development of and ensure alignment with BEC global policies and procedures.

The Essential Requirements Of The Job

  • Minimum of 3 years’ experience in quality manufacturing in either medical devices, automotive, aerospace industry or with background in electro‑mechanical equipment production.
  • Working knowledge with electronic / mechanical components controls and process release and validation elements.
  • Working knowledge in quality management methods (8D, Six Sigma, Statistical Tools, FMEA).
  • Experienced in working within multi‑functional, multi‑regional teams.
  • Fluent in German (B2 or higher) and English.

Preferred Qualifications

  • Solid working knowledge of EU, FDA and related regulations including QSR’s, (FDA 21 CFR 820), ISO 13485 or ISO 9001.

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.

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Stelleninformationen

  • Veröffentlichungsdatum:

    24 Apr 2026
  • Standort:

    München
  • Typ:

    Vollzeit
  • Arbeitsmodell:

    Vor Ort
  • Kategorie:

  • Erfahrung:

    2+ years
  • Arbeitsverhältnis:

    Angestellt

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