Validation Engineer Medical Devices (PACA France)
We are currently recruiting a Validation Engineer to join a fast-growing Medical Device company based in the PACA region.
This role sits at the core of industrialization and compliance activities with a key responsibility in process and system validation.
You will be involved in:
defining and driving validation strategies (process & software)
executing validation activities (IQ/OQ/PQ FAT/SAT)
preparing validation protocols and reports
managing Change Control and CAPA
supporting industrialization and continuous improvement projects
Working closely with R&D QA/RA and Production teams you will play a critical role in ensuring process robustness and regulatory compliance (MDR ISO 13485 FDA).
Profile:
experience in validation within a regulated environment
strong knowledge of MDR / ISO 13485
hands-on structured and project-oriented mindset
Ideal role for a candidate looking to work in a technical cross-functional and high-impact MedTech environment.
Validation Engineer Medical Devices (PACA France) We are currently recruiting a Validation Engineer to join a fast-growing Medical Device company based in the PACA region. This role sits at the core of industrialization and compliance activities with a key responsibility in process and system valid...
Validation Engineer Medical Devices (PACA France)
We are currently recruiting a Validation Engineer to join a fast-growing Medical Device company based in the PACA region.
This role sits at the core of industrialization and compliance activities with a key responsibility in process and system validation.
You will be involved in:
defining and driving validation strategies (process & software)
executing validation activities (IQ/OQ/PQ FAT/SAT)
preparing validation protocols and reports
managing Change Control and CAPA
supporting industrialization and continuous improvement projects
Working closely with R&D QA/RA and Production teams you will play a critical role in ensuring process robustness and regulatory compliance (MDR ISO 13485 FDA).
Profile:
experience in validation within a regulated environment
strong knowledge of MDR / ISO 13485
hands-on structured and project-oriented mindset
Ideal role for a candidate looking to work in a technical cross-functional and high-impact MedTech environment.
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