Bruker Corporation

Quality Assurance Operator (Devices) (m/f/n)

Arbeitsort DE-BW-Nehren
Datum der Veröffentlichung 1 month ago(10/29/2020 6:55 AM)
Anzahl offener Funktionen
Regular Full-Time


The Quality Assurance Operator (Devices) will work within a busy Quality Assurance department to test and maintain the quality of various medical device grade scientific instruments, including DNA extraction machines, PCR instrumentations and associated devices and accessories, allc arried out under ISO13485:2016 quality standard. They will be directly involved in incoming and outgoing control of instrumentation, accessories and PCs, as well as labelling and shipping processes. They will serve as a direct contact for suppliers into the company, create and montior quality documentation and take responsbility for change requests, SCARs, CAPAs and related opimisation processes.



Job duties will include the following tasks:

  • Incoming/Outcoming control of Instruments, Accessories, including functional testing
  • Configuration of Instruments & Computers
  • Control of the relevant change control and improvemtn procedures: SCARs, CAPAs, Change controls, Change requests
  • Product and component labelling
  • Act as main contact person for various suppliers, especially for production and quality aspects
  • Creation and monitoring of quality documentation under ISO13485:2016 QMS
  • Process optimization
  • Allocation of Instruments


  • Personal:
  • Communication skills and precise diction
  • Strong Germand and English langauge skills
  • Ability to work independently
  • Ability to prioritize and monitor tasks
  • Accurate and precisely work
  • Qualification:
  • Degree in Medical technology, biotechnology or a comparable degree; B.Sc., B.Eng., M. Sc., M.Eng. or equivalent industrial experience in this area
  • Good technical/electronic understanding
  • Good PC skills
  • Good knowledge of Windows 10 & Office
  • Other:
  • Knowledge and experience SAP would be extremely beneficial
  • Knowledge and experience of PCR instrumenation would be a distinct advantage
  • Experieince of under an ISO13485:2016 Quality Management System is desirable


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