Ihre Aufgaben

• 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 non-conformances regarding Quality systems, design and manufacturing

Ihre Qualifikationen

• Industrial practice in CAPA process in medical device or pharmaceutical industry
• Knowledge of regulation and standards like ISO 13485, 21 CFR 820
• Fluent English and German

• Experience in Six Sigma (Black Belt/ Green Belt)
• Technical education (engineering degree)