Quality Endodontic Distributors Ltd

About the Company

Quality Endodontic Distributors Limited was founded in 1989 as a wholesaler selling Maillefer products from Switzerland. The range consisted of endodontic instruments, post systems and burs. Our company was the first specialist wholesaler majoring in endodontic products. After eight years of continued sales growth within the UK, the Maillefer company was sold to Dentsply, their largest customer. Dentsply, the new owners, wanted to distribute this fantastic product range themselves. QED, as we had become known, had to change quickly. We decided to become a retailer. As well as selecting a range of products from the Maillefer catalogue, we researched other endodontic suppliers and began to build what is now the widest and best selection of products available from any company in this field. At the same time, we began to build our first sales team. From the start, we worked to ensure that they had a sound knowledge of endodontics, and continued on-the-job training enhanced their expertise. Our sales team today provides valuable information and advice to our customer base. This is backed up by our in house team of dedicated personnel who in each department make sure that the whole process of customer care works as one machine

Listed Jobs

Company Name

Quality Endodontic Distributors Ltd

Job Title

Quality Consultant

Job Description

Job Title: Quality Consultant Role Summary: Provide independent quality management consulting for a small‑to‑medium medical device distributor. Drive ISO 13485:2016 implementation, compliance with UK Medical Device Regulations and EU MDR, and continuous quality improvement. Expectations: - Contract role beginning January 2026. - Approximately 2 on‑site days per month plus remote support. - Availability to attend annual SGS audits. Key Responsibilities: - Conduct Internal Audits and verify compliance with ISO 13485:2016. - Manage Document Control, CAPA, and Non‑Conformance processes. - Set, monitor, and report on Quality Objectives. - Prepare and chair Management Review meetings. - Provide general quality advice and support to business operations. - Facilitate annual SGS audit preparedness and follow‑up. Required Skills: - In‑depth knowledge of ISO 13485:2016, UK Medical Device Regulations, and EU MDR. - Proven consulting experience with small‑to‑medium size medical device businesses. - Strong audit, CAPA, document management, and quality improvement skills. - Ability to deliver practical, scalable quality solutions. - Excellent communication, facilitation, and stakeholder‑management skills. Required Education & Certifications: - Minimum qualification in Engineering, Life Sciences, or related field (Bachelor’s degree). - ISO 13485:2016 Lead Auditor and/or Quality Management System Consultant certification. - Additional certification in Medical Device Quality Management (e.g., CQM) preferred.

Peterborough, United kingdom

On site

02-12-2025