Validation Engineer

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.

Responsibilities:

• 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.