Quality & Regulatory Manager-Medical Devices

Zürich  ‐ Vor Ort
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Schlagworte

Beschreibung

My client has an urgent requirement for Quality & Regulatory Manager-Medical Devices for a contract role in Zurich

  • Looking for a Mechanical Engineer (or any suitable engineer) who has experience in Complaint investigation as against Quality & Regulatory Manager who might have some technical knowledge.

  • Nature of work would include - Understanding the complaint, going through previous audit reports, investigate the device for any issue, try to visualize the kind of issue that might have occurred in an operation theatre, work with the teams to resolve, finish all associated paper work for quality & regulatory purposes

Requirements:

  • Complaint handling specialist for medical devices

  • Structured investigation to find the cause for a complaint

  • Analyzing risk management documents, test certificates, etc.

  • Regular reportings, trendings, accurate data analysis

  • Experienced in working with Trackwise

  • Documentation of results

  • CAPA knowledge/experience

  • Very good English

  • Good German preferred

  • Experience in complaint handling of complaint investigation/(post market surveillance)

  • Experience in quality management, technical/mechanical background

  • Team spirit, open-minded, problem-solver

Contract Duration: 6 months

Project location: Zurich

Contract rates: Market Standard

If interested, please share your updated CV and contact number or call Pooja Rajpal

Start
ab sofort
Dauer
6 months
Von
GIOS Technology Limited
Eingestellt
12.04.2014
Projekt-ID:
694754
Vertragsart
Freiberuflich
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