- Play a key role in ensuring top‑tier product quality and safety.
- Evolving in a in a fast‑growing med‑tech environment.

**About Our Client**
Our client develops technologies designed to improve the quality of life for individuals with injuries. The company operates in a mission‑driven, collaborative environment focused on innovation, patient impact, and continuous improvement.


**Job Description**

- Manage product reception and perform incoming inspection activities.
- Identify and report non‑conformities using the appropriate documentation and channels.
- Handle product returns to suppliers, both digitally and physically.
- Oversee the Quality storage area, including quarantine and release zones.
- Prepare work orders and associated documentation such as travelers and traceability records.
- Ensure operators are trained on Quality and Manufacturing procedures.
- Perform Device History Record (DHR) reviews, including GDP compliance and traceability.
- Support final product release alongside the Quality representative.
- Contribute to continuous improvement for components, sub‑assemblies, finished products, and related processes.
- Participate in supplier quality management activities in collaboration with the Supplier Quality Engineer.

**The Successful Applicant**

- Bachelor's degree or equivalent in a scientific or engineering discipline.
- 5-10 years of experience in Quality Control within the medical device industry.
- Skilled in inspection, testing and analysis using quality control tools and techniques.
- Strong knowledge of ISO 13485, FDA QSR and regulatory requirements.
- Ability to read and understand technical drawings.
- Solid manufacturing technical background.
- Proficient in IT tools such as Microsoft Office, ERP or SAP.
- Excellent communication and interpersonal skills; able to work autonomously with rigor and flexibility.
- Strong team orientation, analytical mindset and problem‑solving abilities.
- Fluent in English; French is an advantage

**What's On Offer**

- A key individual contributor role with high impact on product quality and compliance.
- The opportunity to work in a mission‑driven organisation at the forefront of medical innovation.
- A 6-month mission in a dynamic, collaborative environment supporting continuous improvement and professional development.

**Contact: Marion Buttay**
**Quote job ref: JN-032026-6971490**