We are looking for a Quality Engineer - Investigations (NCMR) for our client specializing in medical devices in the canton of Vaud.
Temporary 6-month (possibility to extend).
Starting date : ASAP !
( Mandatory experience in investigation in production site)
Your Tasks:
Manage and coordinate activities related to Corrective and Preventive Actions (CAPA) and Non-Conformances (NCMR).
Conduct root cause analysis, risk assessment, and ensure the implementation and effectiveness of corrective actions.
Monitor quality metrics to identify systemic issues and improve processes.
Support supplier investigations and internal/external audit activities.
Ensure compliance with applicable regulations (ISO 13485, FDA, MDR, etc.).
Your Profile:
Bachelor's degree in Engineering or Physical Sciences (or equivalent experience).
Mandatory experience in investigation in production site
Minimum 5 years of experience in the life science industry.
Strong knowledge of quality tools (CAPA, Six Sigma, non-conformance management).
Familiarity with ISO 13485, FDA, and MDR regulations.
English and French
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