EMS is a global leader in the design, manufacturing, and distribution of precision medical devices used in dental prevention, pain therapy, and urology. With over 40 years of expertise, EMS delivers innovative solutions across three key medical fields:
* Dental Prevention – Inventors of Guided Biofilm Therapy (GBT), an evidence‑based protocol for biofilm management
* Pain Therapy – Leaders in shock wave technologies for musculoskeletal treatments
* Urology – Market leaders in endoscopic lithotripsy
Driven by our core values—Respect, Excellence, and Client Orientation—we are committed to delivering clinically proven, minimally invasive treatments that improve patient outcomes worldwide.
MISSION
As a Quality Engineer, you will report to the Quality Assurance Group Leader and play a key role in supporting and improving EMS’s Quality Management System.
You will contribute to both R&D and production quality activities, ensuring compliance with applicable regulatory requirements, including ISO 13485, while supporting continuous
improvement across the organization.
In addition, you will contribute to Environment, Health & Safety (EHS) topics in coordination with internal stakeholders, as part of a shared responsibility model within the organization.
TASKS & RESPONSIBILITIES
Quality Management & Compliance
* Support and improve the Quality Management System, ensuring compliance with applicable standards (including ISO 13485 and MDR) and audit readiness
* Contribute to internal and external audits and support follow‑up actions
* Maintain and improve quality documentation, processes, and procedures
R&D & Product Quality
* Support R&D projects by ensuring quality and regulatory requirements are integrated throughout the development lifecycle
* Contribute to risk management and design control activities
* Provide quality guidance during design, verification, and validation phases
Production & Operational Quality
* Manage non‑conformities and support root cause analysis and CAPA processes
* Contribute to change management activities impacting products and processes
* Collaborate closely with Production, Supply Chain, and other departments to ensure product quality and process robustness
* Drive continuous improvement initiatives across operations
EHS Contribution
* Contribute to EHS‑related topics in collaboration with internal stakeholders
* Support the implementation and follow‑up of EHS practices and procedures
* Participate in risk awareness and continuous improvement initiatives related to workplace safety and environment
* Act as a point of coordination for EHS topics within the scope of your activities
EDUCATION & PERSONAL SKILLS
* Degree in Engineering, Quality, or a related field
* Minimum 3 years of experience in a Quality role within a regulated or industrial environment
* Experience in medical devices is a strong advantage
* Good understanding of quality standards and regulatory environments (including ISO 13485 and MDR)
* Familiarity with quality tools such as CAPA, risk management, and change control
* Strong analytical and problem‑solving skills
* Ability to work cross‑functionally and communicate effectively
* Structured, rigorous, and detail‑oriented mindset
WHY JOIN EMS?
At EMS, you will join a dynamic and international environment where quality and innovation are at the core of everything we do. You will have the opportunity to work on impactful products, collaborate with multidisciplinary teams, and contribute to continuous improvement in a regulated and fast‑evolving industry.
#J-18808-Ljbffr