Supplier Quality Engineer - (M/F)
Fast Track Diagnostics Luxembourg S.à r. l.
Esch-sur-Alzette, LU
il y a 1j
source : Monster

Do you want to help create the future of healthcare? Our name, Siemens Healthineers, was selected to honor our people who dedicate their energy and passion to this cause.

It reflects their pioneering spirit combined with our long history of engineering in the ever-evolving healthcare industry.

We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally.

Sound interesting? Then come and join our global team as Supplier Quality Engineer - (M / F) to be responsible for representing supplier quality in product development projects and supplier management.

Your main tasks and responsibilities : You will responsible for providing supplier quality expertise as well as creating, reviewing, and approving supplier quality documentation to ensure compliance with internal procedures and regulatory requirements for in-vitro diagnostics and medical devices.

You will manage quality and supplier quality engineering process and will utilize his / her prior experience in both supplier management and quality engineering in the IVD industry to develop and maintain key processes, while adhering to regulatory requirements You will be responsible for providing adequate level of oversight with suppliers and OEMs, as well as ensuring that procurement, product development, and manufacturing processes are meeting business goals and quality standards.

  • You will develop relationships and interfaces with suppliers to maintain positive performance and hold suppliers accountable when business or quality needs are not met You will ensure supplier audit and Supplier Corrective Action Request (SCAR) processes are implemented effectively To find out more about the specific business, have a look at Your qualifications and experience : Minimum BA / BS in scientific discipline (Engineering, Molecular Biology or Biochemistry preferred) 4+ years’ experience in a supplier quality engineering AND / OR design / manufacturing quality engineering role at a IVD or MD Manufacturer Knowledge of applicable US (21 CFR 820) and EU (ISO 13485) quality system requirements Lead Auditor experience per ISO 13485 and / or FDA QSIT audits is consider as an asset Your attributes and skills : You are a driven individual with a history of developing collaborative, cross-functional solutions You have highly developed writing and interpersonal skills with the ability to work with international teams You have working knowledge of common computer software applications (SharePoint, SAP, WORD, EXCEL, Adobe Acrobat, etc) You have excellent written and spoken English language skills You have capacity for working independently and excellent interpersonal and organizational skills You are willing to travel + / - 30% Our global team : Siemens Healthineers is a leading global medical technology ;
  • 50,000 dedicated colleagues in over 70 countries are driven to shape the future of healthcare. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services.

    Our culture : Our culture embraces different perspectives, open debate, and the will to challenge convention. Change is a constant aspect of our work.

    We aspire to lead the change in our industry rather than just react to it. That’s why we invite you to take on new challenges, test your ideas, and celebrate success. Check our Careers Site at

    Mon email
    En cliquant sur « Continuer », je consens au traitement de mes données et à recevoir des alertes email, tel que détaillé dans la Politique de confidentialité de neuvoo. Je peux retirer mon consentement ou me désinscrire à tout moment.
    Formulaire de candidature