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CAPA Consultant - Quality Process in Pharmaceutical Industry

Eingestellt von Whitehall Resources Ltd

Gesuchte Skills: Engineering, Consultant

Projektbeschreibung

CAPA Consultant required to support the owners and the site CAPA Coordinator team for appropriate Investigation and Root Cause Analysis, definition of appropriate actions (corrections, corrective actions, preventive actions) with including the required documentation according to regulation 21 CFR 820.100.

The CAPAs deals with nonconformances regarding Quality systems, design and manufacturing.

What we require from the candidate:
- Industrial practice in CAPA process in medical device or pharmaceutical industry
- Knowledge of regulation and standards like ISO 13485, 21 CFR 820
- German speaking essential

Further the following would present a considerable advantage:
- Experience in Six Sigma (Black Belt/Green Belt)
- Technical education (engineering degree)

Projektdetails

  • Einsatzort:

    Zug, Schweiz

  • Projektbeginn:

    asap

  • Projektdauer:

    12 months

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

Whitehall Resources Ltd