Quality Assurance Officer

This is a great role for someone at the start of their career as part of a QMS team, with some experience of medical device development. As part of the Management System team you will support the company in compliance to CDP’s Quality and Information Security Management Systems (QMS and ISMS) by undertaking the following activities:

• Monitoring and maintenance of the:​
• Non-conformance system
• Corrective Action Preventive Action system
• Opportunities for Improvement system
• Change Control system
• Customer Complaints system
• Supplier Control system
• Document control for the management system and for Projects
• Authoring updates to management system documentation
• Administration of the Internal audit system, including scheduling, management of internal audit reports, and raising findings in the eQMS
• Perform Internal auditing team to ensure compliance with SOPs and quality standards
• Coordination of certification audits and client audits or evaluations of CDP as a supplier, including booking relevant calendars, organising rooms and people according to agendas, support during the audit and other activities as required
• Standards library maintenance, including checking and approving new requests, making purchases, and managing the renewal process
• Coordination and support for Management Review meetings, including booking relevant calendars, minute taking, tracking actio