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Product Vigilance Specialist (f/m) in Selzach at Stryker Corporation

Date Posted: 11/25/2018

Job Snapshot

Job Description

Your key responsibilities

  • As complaint handling specialist for medical devices you are responsible for  the structured investigation of claimed products.
  • You will do device inspection and root cause analyses on these claimed products and based on your findings initiate corrective actions if necessary.
  • Moreover you analyze engineering data, test certificates, risk evaluations, etc. and compile trendings. Your results are then documented in English in the international Stryker database.
  • Regular reporting as well as accurate data analysis is also part of your field of action.

What are we looking for?

  • You successfully completed your studies in a technical field (ideally mechanical engineering, quality management or medical technology) or alternatively you have completed your technical apprenticeship above-average and have already gained some work experience in a regulated environment.
  • Ideally, you already have first experiences in complaint handling of medical devices (post market vigilance) and have had experience with the implementation of corrective actions (CAPA).
  • You have a distinctive passion for technical matters, are an analytical thinker and like to work independently but also in interdisciplinary teams.
  • Very good written and spoken English complete your profile. German and/or French is a plus.


If you have questions regarding the advertised position, please do not hesitate to contact Mrs. Nicole Röll by phone on +49 (0) 4348 702 685. Please notice that the title of this advertisement can differ from the position title.

Work From Home: No

Travel Percentage: None

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