5 of 5 Contract Quality Management Jobs in the South East

client, a leading international organisation operating within the healthcare sector, is looking for a Quality Administrator to join their team on a four-month temporary contract to support the implementation of a new global Quality Management System. This is a fantastic opportunity to gain valuable experience working … major transformation project within a highly regulated business. You'll play a key role in ensuring quality documentation is accurately transferred into the new system, helping maintain compliance and supporting the successful delivery of the project. Responsibilities include: Supporting the implementation of a new Quality Management System ...

validation system lifecycles and strict medical device requirements. Protocol Development: Author, review, and execute robust validation protocols, reports, and technical documentation to meet rigorous quality standards. Change Control Management: Provide expert guidance on validation changes and lead change control activities in accordance with established quality management system (QMS) procedures. General QA Support: Collaborate closely with the wider Quality Assurance team to support audits, risk assessments, and continuous improvement initiatives. What We Are Looking For Regulated Industry Experience: Experience working within a strictly regulated environment (highly prefer medical devices under ISO 13485/ ...

Solution Architect delivering robust SAP enterprise solutions. Domain Knowledge: Strong experience across core enterprise process domains, ideally including supply chain, maintenance (EAM), and quality management. Manufacturing Fluency: Comfortable navigating and integrating multi-platform manufacturing environments (specifically linking ERP to MES/PLM). Intrigued? If you are an independent ...

troubleshoot analogue and digital electronic circuits, including Op-Amps and reference ICs. Accurately document test results and maintain traceability in accordance with ISO 9001 quality standards. Complete detailed testing procedures, with each unit taking approximately one hour to test. Ensure compliance with IPC standards and ESD procedures within … detail with accurate documentation and reporting skills. Desirable Skills Experience working within the medical device or healthcare electronics industry. Familiarity with ISO 9001 quality management systems and documentation requirements. Previous experience dismantling, repairing, or testing complex electronic assemblies. Experience working within regulated manufacturing or engineering environments. ...

activities at the medicinal product level with key stakeholders in clinical trial teams Utilise up-to-date data from multiple medicine sources to identify quality risks Guide medicine business partners in developing mitigation plans to address identified risks Responsible for reporting risk management information to key stakeholders throughout … degree in a scientific subject or have equivalent working experience. Working experience in GxP environment within the pharmaceutical industry. Proven knowledge in project management including experience in quality risk management. Proficient experience with clinical trials, clinical research associate, clinical trial management. Demonstrated experience in leadership and strategic problem ...