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. We aim to serve new generations and promote fresh perspectives on life for ourselves, for you, and for your patients. For nearly a century, we have continuously reinvented what we thought we knew. We are dedicated to fostering a culture of performance that promotes equity, loyalty, and respect.
We embrace change that empowers us to revolutionize endodontics. Our focus is to make endodontics safe and easy through innovative, high-quality, and less invasive solutions.
Join Our Quality Team as a Quality Engineer
Role Mission
Participate in the development and deployment of our quality management system while reporting on its effectiveness and identifying areas for improvement, both in manufacturing and with suppliers.
Your Responsibilities
- Contribute to the efficient operation of the quality department and maintain certifications for the company and its products.
- Actively engage in the continuous improvement of our quality management system and organizational processes.
- Ensure effective communication with external contacts, customers, suppliers, and other departments, providing support on all quality assurance matters.
- Raise awareness of applicable regulatory and quality management system requirements, contributing to training company employees on these aspects.
- Lead quality projects, including the integration of new requirements into our QMS, validation of manufacturing processes, and CAPA processing.
- Participate in all quality department activities such as conducting internal and supplier audits, handling customer complaints, and managing document modifications.
- Coordinate the processing of internal and supplier non-conformities.
- Collaborate with technical and production departments on quality-related challenges, including problem-solving, process improvement, and new production equipment development.
Your Profile
- Higher education in science or engineering.
- Minimum of 3 years of professional experience in quality management within medical devices.
- Familiarity with key standards and regulations in 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 eQMS (electronic quality management system) is a plus.
- Proficient in MS Office tools (Word, Excel, PowerPoint).
- Good command of spoken and written English (B2 level).
- Strong team spirit.
- Excellent analytical skills.
- Pragmatic, proactive, and rigorous approach.
- Outstanding communication and interpersonal skills.
We Offer
- A stimulating and dynamic work environment at the forefront 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 work hours, a minimum of 5 weeks’ vacation, and contribution towards health insurance.
Entry into Function
Immediate or to be agreed.
If you recognize yourself in this job description, are dynamic, and interested in tackling challenges within a growing company, we invite you to apply online using the form below.
Please note that only applications matching the job profile will be considered.