QC Analyst - GC Europe - Louvain

GC Europe

Région

Louvain

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: You mainly perform 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 analyses official complaint. After investigating a complaint you are able to write a brief report of your findings and conclusions.
  • Non conformity: 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 analyse data via excel, make trends/graphs and detect anomalies.
  • Continuous improvement: You participate 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 analyses/Validation: You participate in preparing, performing and documenting FMEA analyses and validation of new/changed equipment/processes.

Who are you?

Hard skills

  • 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
  • Overall, you are a customer- and quality-orientated person.
  • You are areal team player who easily communicates with all stakeholders
  • You are able to manage independently your daily tasks/goals.
  • Sap knowledge (QM module) is a plus

What do we offer you?

  • A challenging job with potential for growth in an international and diverse company.
  • A permanent contract with full time employment.
  • Flexible hours.
  • Competitive salary package.
  • Stunning offices and a great company culture, based on respect and comradeship.
  • An opportunity to contribute to a better, healthier world in collaboration with colleagues who are passionate about what they do.

Who are we?

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 is located at the Researchpark Haasrode in Leuven. GC Europe NV supports and leads our different sales offices and dealers. Our warehouse spreads our products to Europe and the Middle East. Next to this we produce some leading products for dental technicians.


Interested?

When applying, be sure to upload your CV and motivational letter to your profile!

Contact person:

Ansje Vanbeselaere
Recruiter
+32 472 18 42 49
GC Europe

Société

GC Europe