Qc Analyst

**GC Corporation** was founded in 1921 in Japan and has developed itself into one of the most prominent companies in the development, production, and distribution of a very wide range of dental products. Since 1972 **GC Europe NV,** our European Headquarter is located at the Researchpark Haasrode in Leuven. GC Europe NV supports and leads our different sales offices and supports authorized dental dealers. Our warehouse distributes our products throughout Europe, Middle East, and Africa. Additionally, we offer state of the art products and systems for dental technicians.

We are currently looking for a:
**QC Analyst**

**Purpose of the job?**

As

**QC Analyst**

you are responsible for controlling all quality aspects in our production of dental materials, located in Leuven. The production exists out of following sections: investments, stones, Glass Ionomer, composite, Assembly and scanner department. Besides quality control and release, QC is also responsible for calibration and validation of equipment and processes.

**What is your mission?**
- Quality inspection: physical/chemical and mechanical tests (incoming; intermediate and finale release) in the lab on dental products manufactured on site according ISO standards and internal procedures
- Document control: you are responsible for monitoring and archiving of quality records
- Calibration: monitoring of external and performance of internal calibration of all production/QC related measuring devices
- Complaint handling: in close collaboration with the supervisor QC, production and complaint officer you analyze official complaint. After investigating a complaint you are able to write a brief report of your findings and conclusions
- Non conformity: you are responsible to document and investigate deviations of the standard operating procedures. You report non conformities and follow up actions
- Trouble shooting: you participate in the monitoring and daily troubleshooting of the QC-lab

You are responsible for keeping careful note of the raw data: you are able to analyze data in Excel, make trends/graphs and detect anomalies.
- Continuous improvement: participation in implementing and improving the QC control systems and/or other processes. For this you will work in close contact with associates of other departments
- Risk analysis/Validation: participation in preparing, performing and documenting FMEA analysis and validation of new/changed equipment/processes

**Who are you?**
- You are a Bachelor in chemistry with interests in the dental field (or equivalent)
- Knowledge of GMP / medical devices ISO13485/ MDR / Quality Systems
- 5S/ Kaizen methodology
- Able to write reports in English : this can be project-, test
- and/or validation reports
- Good computer skills: Word, Excel, Power Point
- Knowledge of Dutch and English is a must
- Customer
- and quality-oriented personality
- Team player who easily communicates with all stakeholders
- Able to manage independently your daily tasks/goals
- SAP knowledge (QM module) is a plus

**We offer you**
- Competitive salary package including meal vouchers
- Hospitalization and group insurance
- An opportunity to contribute to a better, healthier world in collaboration with colleagues who are passionate about what they do
- Great company culture, based on respect and comradeship

**Interested?**

When applying, be sure to upload your CV and motivational letter to your profile
- GC is an equal opportunity employer that evaluates applicants regardless of their race, nationality, gender, age, or disability._