QC Analyst

As QC analyst you are responsible for controlling all quality aspects for the production of dental materials. 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.

Interested in this challenging job?

Make your appointment online at www.konvert.be send your CV to leuven.interim@konvert.be 

• 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

• A challenging job with potential for growth in an international and diverse company.
• 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.