About Us
FKG Dentaire Sàrl – a Henry Schein company - is a leader in the development, manufacturing, and distribution of high-precision dental products tailored for dentists, endodontists, and laboratories. Our mission is to continuously innovate our approaches to work: creating solutions that are more respectful, efficient, agile, ergonomic, and safer for new generations, promoting fresh visions for us, for you, and for your patients. For nearly a century, we have consistently redefined what is possible. We are dedicated to fostering a culture of performance built on equity, loyalty, and respect.
Embracing change is at the heart of our philosophy, empowering us to revolutionize the field of endodontics with safe and easy solutions through innovative, high-quality, and minimally invasive products.
Position: Quality Engineer
Role Mission:
Participate in the development and deployment of our quality management system, evaluating its effectiveness and identifying areas for improvement within both manufacturing and supplier environments.
Your Responsibilities:
- Support the quality department's operations and maintain certifications for the company and its products.
- Actively contribute to the continuous enhancement of our quality management system and overall organization.
- Facilitate effective communication with external contacts, customers, suppliers, and other departments related to quality assurance.
- Raise awareness of applicable regulatory requirements and quality management system necessities, and contribute to training programs for company employees.
- Lead quality initiatives, including the integration of new requirements into our Quality Management System (QMS) and validation processes.
- Engage in departmental activities such as conducting audits, addressing customer complaints, managing document revisions, and analyzing quality data.
- Coordinate the handling of internal and supplier non-conformities.
- Collaborate with technical and production teams on quality-related challenges such as problem-solving, process improvements, and the development of new production equipment.
Your Profile:
- Advanced degree in science or engineering.
- At least 3 years of professional experience in quality management within the medical device sector.
- Familiarity with primary standards and regulations, including ISO 13485:2016, Regulation (EU) 2017/745, and 21 CFR Part 820.
- Understanding of statistical techniques related to process control, inspections, and sampling plans.
- Experience with electronic Quality Management Systems (eQMS) is a plus.
- Proficient in MS Office tools (Word, Excel, PowerPoint).
- Strong command of spoken and written English (B2 level).
- Team-oriented mindset complemented by excellent analytical skills.
- Exhibits pragmatism, proactivity, and rigor in work.
- Outstanding communication and interpersonal abilities.
We Offer:
- A stimulating and dynamic work environment at the forefront of industrial automation.
- Professional development and career advancement opportunities.
- A collaborative and inclusive corporate culture that values innovation and teamwork.
- Attractive benefits including free parking, remote work options, flexible hours, a minimum of 5 weeks’ vacation, and health insurance participation.
Entry into Function:
Immediate start or to be agreed upon.
Apply online using the form below. Only applications matching the job profile will be considered.