Start your application for this job today
Apply NowStart your application for this job today
Apply NowTEC Partners is pleased to have partnered with a pioneering medical device company dedicated to improving the quality of life for patients through next-generation orthopedic implant devices.
Through events, resources, and patient information, my client aims to empower both medical professionals and patients on their journey to improved orthopedic health.
Quality SpecialistAs the Quality Specialist, you will play a pivotal part in upholding the company's commitment to quality and compliance with ISO 13485 standards.
As a key member of the quality assurance team, you will be responsible for conducting internal audits, leading lean manufacturing initiatives, driving supply chain improvements, and conducting supplier audits to ensure the highest standards of product excellence.
Quality Specialist Responsibilities: Conduct internal audits to ensure adherence to quality management systems and regulatory requirementsLead lean manufacturing initiatives to optimise processes and drive operational efficiencyCollaborate with cross-functional teams to identify areas for improvement and implement corrective actionsDrive continuous improvement initiatives throughout the supply chain to enhance product quality and reliabilityConduct supplier audits to evaluate performance and ensure compliance with quality standards and regulatory requirementsDevelop and maintain documentation related to quality management systems and regulatory complianceProvide guidance and support to team members on quality assurance processes and best practices Quality Specialist Requirements: Bachelor's degree in a Scientific related field or equivalent experience in a commercial manufacturing organisationMinimum of 3 years of experience in quality assurance within the medical device industryStrong knowledge of ISO 13485 standards and regulatory requirementsExperience conducting internal audits and supplier auditsProficiency in lean manufacturing principles and process improvement methodologiesExcellent communication and interpersonal skillsAbility to work effectively in a fast-paced, dynamic environment and collaborate with cross-functional team If you are passionate about quality assurance and committed to driving excellence in orthopedic implant devices, please apply with an up to date CV