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QA - Documentation Specialist in Zürichhorn, Zurigo, Switzerland

Zürichhorn, Zurigo, Switzerland
Job type
Job Id
Posted on
13 Apr 2017
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About the Role:

For my client, an innovative Medical Device Company, based in the Zürich Area, i am looking for a Medical Device- QA Documentation Specialist for the following responsibilities:

Document review

  • Review of Test Protocols, Test Reports, TMT documents, Design documents, Master Validation Protocols, V&V Reports
  • content review, making sure that the documents are in good standardised quality


  • Data Record analysis (NC, complaints, supplier corrective actions, etc.)
  • Creation of Templates
  • Implement new reports, writing SOPs

Your qualifications:

  • 2-5 years working experience in Medical Devices (ISO 13485, FDA & MDD)
  • Documentation Experience
  • Experience in reviewing of technical document's in the Medical Device industry
  • Experience with reporting and creation of different reports
  • English must, German is nice to have
  • Very good excel knowledge
  • European passport

The project start is end of April beginning of May, with a project duration of 2-3 months, with potential extension.

If you are interested in working in an innovative environment based in Zürich, being able to take your own responsibility's, then this might be the perfect short assignment for you.

I am looking forward hearing from you until Tuesday 18/03 and if possible, please update your CV according to the job requirements in order to increase your chance for a an interview.

Best Regards

Sabina Keel

Senior Candidate Relationship Manager

Medical Devices Pharma & Biotech

Real Ein Geschäftszweig der SThree GmbH Talstrasse 65


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