QA Engineer - Investigations.

Job Details

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Job Details
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 ! 


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.
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 ! 


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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VD

Victoria Desvigne

Danke für die Anmeldung zu persönlichen Job-Benachrichtigungen.