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Senior Auditor [ISO 13485 & 21 CFR 820]

Eingestellt von Randstad (Schweiz) AG

Gesuchte Skills: Client

Projektbeschreibung

Dear Auditor,

I'm supporting my medical device client to find an experienced English speaking Auditor to join them in the Quality and Compliance Department starting ASAP until the end of this year. An extension is possible depending on the candidate's suitability to the company and the role itself.

Project Description

As an Auditor in this project you will audit production and technical areas according to the ISO 13485 and 21 CFR 820 regulations. You will write the result reports and review corrective action plans.

I'm looking for an auditor who's able to independently plan and conduct reviews/audits of documentation, as well as collecting and analysing data. Any of your inspection and audit findings you will communicate with professional staff and leadership departments.

For this project it is imperative that you are the owner of a Lead Auditor qualification.

Are you also able to plan ahead and work on multiple tasks with limited supervision?

Do you have strong analytical and problem-solving skills?

Do you work well in a high-paced environment?

Within this role you will be able to connect with other experts in their field, as well as sharing but also gaining knowledge.

If you're looking for a short-term contract with a possibility for extension, please click on the apply button.

I look forward to receiving your application!

Charlotte

Projektdetails

  • Einsatzort:

    Zuchwil, Schweiz

  • Projektbeginn:

    asap

  • Projektdauer:

    End of 2016

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

  • Kategorie:

    IT Entwicklung

  • Skills:

    client

Randstad (Schweiz) AG