Quality Engineer

il y a 1 jour

Montpellier, France Kinvent Temps plein

Our playground? Rehabilitation, sports training and research Our mission is to create revolutionary measuring instruments to support health and sports professionals.

We are currently technological leaders on the world market, equipping teams from Ligue 1, TOP14 and American teams, but above all, we support physiotherapists in their mission to accompany, involve and help their patients progress.

If you share our passion for health, sport and rehabilitation, join our team and contribute to our expansion and success.

We are currently looking for a QA engineer to work cross-functionally with out French & Greek teams.

QA engineer

In this position, you will be at the heart of our quality management system. You will be in charge of keeping up with existing material while setting new process to support our growth. This role is transversal and will require frequent travels between our factory in Thessaloniki(Greece) and our headquarters in Montpellier (France) to ensure procedures are well implemented.

In close collaboration with the hardware and R&D teams, you will be in charge of:
**Quality system management**:

- Follow up, coordinate and update our quality management system (ISO)
- Ensure compliance with current labels and certifications
- Guarantee quality assessment and compliance with international standards
- Create files, documents and process to obtain new certifications to support our sales & industrial strategy
- Identify, analyze actions to define CAPA, especially on non-compliant matters
- Set up guides and quality check procedures to streamline process
- Keep our procedures up to FDA & EUMDR regulations
- Track performance of implemented process by checking or creating new KPIs
- Create reports, market surveillance items to manage risks

**Internal coordination**:

- Share and document process to train internal teams
- Sensibilize teams on procurement, quality and labels matters
- Follow up with complaints : assisting with customer success requests, clinical reports,trials and aftersales
- Act as the person of contact to answer to any quality matter with internal (sales, tech, factory teams) and external stakeholders (label institutions, customers )

Profile

**Mandatory**:

- Exp ISO following
- Customs certificate
- Technical writing & testing
- Background in engineering/electronics/ biomedical
- Problem-solving and analytical skills
- Min 3 years of professional experience in an industrial environment
- A first experience in a medical company would be a great plus

**Languages**:

- English : mandatory
- French/Greek would be a plus

**Job Type**: Full-time

**Status**: Cadre

**Work Location**: In person

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