About Us
FKG Dentaire Sàrl – a Henry Schein company – is at the forefront of developing, manufacturing, and distributing high-precision dental products for dentists, endodontists, and laboratories. Our mission is to innovate new ways of working that are more respectful, efficient, agile, ergonomic, and safe—serving new generations and promoting new visions of life for us, for you, and for your patients. For nearly a century, we have been constantly reinventing what we thought we knew. We are committed to fostering a culture of performance through equity, loyalty, and respect.
We embrace change that empowers endodontics to truly change the game. Our goal is to make endodontics safe and easy through innovative, high-quality, and less invasive solutions.
Position: Quality Engineer
Role Mission
Participate in the development and deployment of our quality management system, reporting on its effectiveness and identifying areas for improvement for both manufacturing and suppliers.
Your Responsibilities
- Contribute to the smooth operation of the quality department and the maintenance of certifications for the company and its products.
- Actively engage in the continuous improvement of our quality management system and overall organization.
- Ensure effective communication with external contacts—customers, suppliers—and other departments within the company, supporting all matters related to quality assurance.
- Raise awareness about applicable regulatory and quality management system requirements and contribute to training company employees on these aspects.
- Lead quality projects, including the integration of new requirements into our QMS, process validation, and CAPA processing.
- Participate in various quality department activities: conduct internal and supplier audits, manage customer complaints, oversee document modifications, define and monitor performance indicators, and analyze data.
- Coordinate the processing of internal and supplier non-conformities.
- Collaborate with technical and production departments on quality-related issues, such as problem-solving, process improvement, and development of new production equipment.
Your Profile
- Higher education in science or engineering.
- Minimum of 3 years of professional experience in the field of quality applied to medical devices.
- Familiarity with key standards and regulations applicable to our field (ISO 13485:2016, Regulation (EU) 2017/745, 21 CFR Part 820, and other regulations applicable in MDSAP jurisdictions).
- Knowledge of statistical techniques related to process control, inspections, and sampling plans.
- Experience with an electronic quality management system (eQMS) is a plus.
- Good command of MS Office tools (Word, Excel, PowerPoint).
- Proficient in spoken and written English (B2 level).
- Strong team spirit with excellent analytical skills.
- Pragmatic, proactive, and rigorous approach to tasks.
- Outstanding communication and interpersonal skills.
We Offer
- A stimulating and dynamic work environment at the cutting edge of industrial automation.
- Opportunities for professional development and career advancement.
- A collaborative and inclusive corporate culture that values innovation and teamwork.
- Attractive benefits including free parking, home office options, flexible working hours, a minimum of 5 weeks’ vacation, and participation in health insurance.
Entry into Function
Immediately or to be agreed.
Apply Online
If you recognize yourself in this job description, are dynamic, and are interested in taking on challenges in a growing company, we look forward to receiving your application online using the form below. Please note that only applications matching the job profile will be considered.