This role involves leading the regulatory strategy for a cardiology medical device company, focusing on FDA, CE, and UKCA submissions, and ensuring compliance with international regulations. You will work closely with the senior team and regulatory bodies, driving the company's expansion into new markets.
The Quality Manager will lead quality operations, drive standards, and ensure compliance in a precision manufacturing environment. Responsibilities include managing quality activities, maintaining systems, and collaborating with production teams to improve efficiency and safety.
The Quality Manager will establish and own the ISO 13485 Quality Management System (QMS) for Carbometrics, a chemistry company developing cutting-edge sensors. Responsibilities include document control, process improvement, internal and external audits, and building a strong quality culture in a growing team.
The Operational Quality 1 role involves providing front-line quality support in a manufacturing environment, ensuring high standards of quality and compliance. Responsibilities include reviewing and releasing product documentation, managing non-conforming materials, and supporting quality audits and investigations.
This role involves ensuring the quality and regulatory compliance of cloud and embedded software for medical devices, particularly in the context of organ perfusion technology. Responsibilities include developing and maintaining software documentation, risk management, and collaborating with cross-functional teams to meet stringent medical device standards.
This role involves assessing and improving Quality Management Systems for software-based medical devices, leveraging 4+ years of medical device industry experience and ISO 13485 auditing expertise. The position offers remote flexibility and the opportunity to impact high-quality standards.
This role involves performing biochemical analyses on patient samples, maintaining and monitoring equipment, and providing technical advice. The position offers flexible working options and professional development opportunities within a dedicated laboratory team.
This role involves leading monthly product quality monitoring, developing and maintaining Power BI dashboards, conducting complaint investigations, and supporting post-market surveillance activities. You will work closely with cross-functional teams to ensure regulatory compliance and drive continuous improvement in a global medical device company.
The Calibration Engineer will calibrate and verify the performance of ProSim medical simulators at a client’s facility, ensuring accuracy, reliability, and compliance with ISO standards. They will work closely with the client’s laboratory, engineering, and quality teams, maintaining detailed records and addressing non-conformances.
The Calibration Engineer will be based at a key customer site, responsible for calibrating and verifying medical simulators. They will work closely with the customer's engineering and quality teams to ensure equipment accuracy, reliability, and compliance with ISO standards.
The Senior Training & Education Specialist designs, develops, and implements learning solutions to support operational processes, workforce capability, and business performance. The role involves conducting needs analyses, developing curricula, managing projects, and facilitating training sessions across diverse customer and business environments.
The Senior Training and Education Specialist designs, develops, and implements learning solutions to support operational processes, workforce capability, and business performance. The role involves conducting needs analyses, developing curricula, managing learning projects, and facilitating workshops, while ensuring alignment with quality standards and stakeholder expectations.
This role involves providing hands-on regulatory support for a diverse portfolio of complex engineering projects, working closely with design engineers and project teams to ensure compliance with international standards. You will contribute to the quality management system, interpret regulatory requirements, and help navigate compliance considerations while supporting innovation.
Perform physical and analytical stability testing on medical devices and skincare products in a GMP/GLP-compliant laboratory environment. Generate, analyse, and report stability data, support shelf-life claims, and contribute to regulatory compliance and continuous improvement initiatives. Operate and maintain analytical instrumentation while ensuring adherence to quality standards and safety procedures.
This role involves supporting market access, quality systems, and governance in a healthcare and technology environment. Responsibilities include managing regulatory and technical documentation, ensuring CQC compliance, and coordinating evidence for audits and inspections.
The Product Compliance Officer will manage and advance product regulatory compliance for a healthcare technology company, focusing on infection prevention and control solutions. Key responsibilities include monitoring regulations, creating safety data sheets, and advising on product-related activities.
