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Project Engineer R&D – EU MDR Compliance (f/m) - temporary 12.2019 in Selzach at Stryker Corporation

Date Posted: 1/23/2019

Job Snapshot

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Job Description

Your key responsibilities

  • You are supporting us to make our high-end products compliant to the new Medical Device Regulation (MDR) while creating, updating and remediating the Technical Documents with quality and clinical content regarding Hazardous Substances and similar EU MDR requirements.
  • You review, assess and update the PLM system and Databases.
  • You will closely collaborate with the Material Science department, the Quality department as well as the PLM / Data management team to support new registrations.
  • Within the scope of the R&D EU MDR project you will be part of the project team and work closely with related departments working on the same project.

What we are looking for?

  • You hold a degree (higher education or Bachelor Degree) in engineering, Computer Science or equivalent and you have preferably gained 2 years or more of professional experience working in a highly regulated industry (e.g. medical, pharmaceutical, automotive).
  • Ideally you have working experience with Databases (e.g. Excel and Access) and Product Lifecycle Management systems (e.g. Windchill).
  • Apart from your familiarity with PLM systems within a regulated industry you have a basic knowledge of material and chemistry science.
  • You are characterized by analytical reasoning, a focused, pro-active and solution-oriented work style along with a high sense of process thinking and team driving skills.
  • You value an international working environment where you can use your excellent skills of both English and German. Good knowledge of French is an advantage.

We are looking forward to your online application via our career page, reference number R406702.

Please notice that the title of this advertisement can differ from the position title.

Work From Home: Yes

Travel Percentage: None


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