improvement, contributing to continuous improvement initiatives. Qualifications, Skills and Abilities Essential: HND/Graduate level or previous experience in Quality Assurance role Understanding of ISO13485, ISO15189 or ISO9001 requirements Previous experience working with In Vitro Devices (IVD/IVDR) or Medical Devices (MDD/MDR) Attention to detail/concern more »
Qualifications: Demonstrated experience in the design and development of products - Medical industry advantageous Design or Engineering Degree preferred Familiarity with regulatory standards and QMS - ISO13485 advantageous CAD proficient, preferably Solidworks Plastic manufacturing process knowledge If you want to be part of a team dedicated to making a meaningful impact in more »
managing or supporting the management of scientific or engineering projects. Ability to work to the Company’s Quality Systems and Policies in line with ISO13485 standards. Advanced experience with Microsoft Word and Excel. Great communication skills. Be eligible to work full time in the UK without restriction. Excellent work ethic more »
At least relevant technical experience Experience in nucleic acid assay development Commercial in vitro diagnostic product development experience Knowledge of Quality Management & Regulatory frameworks (ISO13485, FDA 21 CFR 820, cGMP) Previous line management experience If you're ready to make a substantial impact in the realm of more »
