Your contribution in the role as Senior QA Manager
You will perform process validation including creation and execution of protocols and reports on supplier side
You will control pFMEA for risks included in the process flow map and update them as required
Your responsibility is to update the reaction plan to prevent non-conforming products
You will perform Test Method Validation(TMV) / Measurement System Analysis (MSA)
Senior QA Manager (f/m)
Minimum a bachelor's engineering degree in life science, materials science or a related field
Minimum seven years' experience in Class II Medical Device manufacturing
Good understanding of the medical device market ( ISO 13485, ISO 14971, 21 CFR Part 820 Subpart G – Production and Process Controls)
Profound knowledge in GMP/GDP, compliance, and validation (CSV, process)
excellent German and English language skills
Further Details Location: Canton Winterthur Start date: 1st of November 2017 Type of contract: Temporary for 6 Month
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