Product Vigilance Specialist (f/m) - 27706BR - EN in Selzach at Stryker Corporation

Date Posted: 6/1/2018

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Selzach
  • Job Type:
    Regulatory Affairs
  • Experience:
    Not Specified
  • Date Posted:
    6/1/2018
  • Job ID:
    27706BR

Job Description

  • 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.

Job Requirements

  • 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.

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