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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