1 to 8 of 8 Permanent Internal Audit Jobs in Oxfordshire

the future of fusion energy. As the Group Auditor , you will play a pivotal role in supporting in the management and implementation of the audit programme including the delivery of audit assignments, validation of audit actions, and preparing reports for presentation at various governance boards. You will … be collaborating with the Group Head of Internal Audit and the Group Systems Audit Manager to drive the business in the development and promotion of a proactive culture for assurance. This role will see you working on a broad array of Auditing functions, providing opportunities for … growth in your professional career. Additional Responsibilities: - Plan, conduct and deliver audit assignments as required. - Proactively engage with stakeholders and supervise the timely close-out of audit actions. - Administer the quality of audit information added to QPulse including the validation of data and submissions to close-out more »

upholding the highest quality standards for products and processes. Key responsibilities include: - Developing and implementing quality system strategies aligned with business goals. - Conducting internal audits and supporting external audits to ensure compliance with ISO 9001 and other relevant standards. - Collaborating with cross-functional teams to resolve quality issues more »

oversight of training on the processes. Review existing company procedures to ensure they meet current regulatory guidelines and make adaptations as necessary. Lead internal audits to ensure consistent compliance. Line management of one Quality Associate. What you'll need to succeed To be considered for the role of more »

and providing timely feedback to Equipment Engineering when necessary. Participate in ensuring all In-process Quality Standards are maintained, helping in Internal Audit Plans and data records [ Batch Route Cards] compliant to existing ISO 9001: 2015 accreditation. Process Control Monitoring using: Microscopy, Electrical Testing, full IPQC and more »

and providing timely feedback to Equipment Engineering when necessary. Participate in ensuring all In-process Quality Standards are maintained, helping in Internal Audit Plans and data records [ Batch Route Cards] compliant to existing ISO 9001: 2015 accreditation. Process Control Monitoring using: Microscopy, Electrical Testing, full IPQC and more »

industries are endless! As a quality engineer, you will be tasked with carrying out customer and supplier facing activities, as well as conducting internal audits and creating documentation to adhere to company procedures and accreditation's. You would be dealing with non-conformities, customer concerns and overseeing quality more »

supply and nomination through occasional site assessments and audits. PPAP approve supplied parts for series production and lead concern resolution with suppliers. Conduct internal audits to ISO 9001:2015 and ISO 14001:2015 standards and support the on-going maintenance of our management system. Create and maintain procedures … and documents as required. Who are we looking for? Recognised technical engineering qualification. Trained internal auditor to ISO 9001:2015. Demonstratable experience of PPAP processes. Strong root cause analysis skills. Working knowledge of metrology techniques. Understanding of engineering drawings and geometric tolerancing. Comfortable viewing CAD/STEP files. more »

senior leadership team To represent Quality on the clinical projects undertaken and be the main QA contact for CROs and GCP Laboratories Perform internal audits. These to include document audits such as Protocols, Investigator Brochure, Clinical Study Reports and regular audits on Trial Master File and Sponsor Oversight … a GCP Quality professional in a management/leadership role within a Pharmaceutical/Biotechnology industry Experience at conducting service provider, site and internal audits highly desirable Experience of building and maintenance of Sponsor Oversight File (SOF) Experience in hosting GCP Inspections Experience in IT Systems validation desirable more »