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Sterility Assurance Specialist, Medical Device, Validation

Eingestellt von Sentinel IT LLP

Gesuchte Skills: Consultant, Client

Projektbeschreibung

My client are a Global Medical Device company based in Switzerland and are looking for a Sterility Assurance Specialist to join their team for an initial 18 month consultant basis. You will be responsible for European Sterility Assurance, ensuring compliance to the Medical Device Directive, ISO 13485, ISO 14971, ISO9001 and FDA regulations. You will create, review and release documents as well as ensuring sterility validations. To be considered for this you should have extensive experience in the Medical Device industry well as being familiar with government regulations including ISO 15883, ISO 17665, ISO 17664. There is an immediate start date available for the right candidate, if you are an experienced Sterility Assurance Specialist looking to work with a global leader on a lucrative 18 month project apply for the advert for consideration, alternatively to discuss in more detail call me.

Projektdetails

  • Einsatzort:

    Solothurn, Schweiz

  • Projektbeginn:

    asap

  • Projektdauer:

    18 months

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

Sentinel IT LLP