23/04/2024 | Fulltime | Birmingham | CV-Library | £36,000 - £38,000 / Year Of the QMS and any needs or opportunities for improvements Reporting and investigating any instances of non-conformance Integrating customer standards into the QMS as required Development, issue and maintenance of inspection standards Extensive liaison with customers on quality issues Liaison with other
Save for laterRegister your CV23/04/2024 | Fulltime | Havant | CV-Library | £53,000 - £55,000 / Year Internal - external auditing skills (qualified - certified in audit management). Strong technical skills with a background in manufacturing (electronic & I or mechanical engineering). Must be familiar with and have a working knowledge of the following standards ISO 9001 (QMS), ISO 14001 (Environmental
Save for laterRegister your CV19/04/2024 | Fulltime | Cambridge | CV-Library | £45,000 - £50,000 / Year To own the QMS for the company standards to ISO 9001 and deliver quality products to the highest standards across all company functions. Main responsibilities for this Quality Engineer - Electronics are - Responsibility for the maintenance of QMS. Keeping up to date with all regulatory requirements
Save for laterRegister your CV19/04/2024 | Fulltime | | Ireland | CV-Library | £80,000 - £110,000 / Year Looking for a QARA manager and RP for a global life science manufacturer. Role will be remote with occasional travel to Dublin area, must be able to work without sponsorship. - Must have experience setting up ISO 13485 QMS. - Must be elligible to act as Responsible Person. - Solid understanding
Save for laterRegister your CV23/04/2024 | Fulltime | Newtown | CV-Library | £50,000 - £55,000 / Year To-day of the role Manage and develop direct reports within the Quality, Regulatory, and Health & Safety teams. Ensure the UK QMS meets all requirements of the business scope, as well as alignment with the corporate QMS. Monitor and interpret regulatory changes to assess their impact on the business
Save for laterRegister your CV18/04/2024 | Fulltime | Cambridge | CV-Library | £40,000 - £60,000 / Year Provides exciting possibilities for ensuring cheaper, faster and more accurate DNA - gene constructs than traditional plasmid-based methods. In a key phase of their growth, our client is looking to hire a QA Manager to oversee a small team to achieve cGMP compliance and develop - maintain their QMS
Save for laterRegister your CV22/04/2024 | Fulltime | Sunderland, Washington (Tyne a | CV-Library | £45,000 - £50,000 / Year An established company on a permanent basis. The job will include - Leading continuous improvement activities. - Leading analysis and problem-solving activities (8D, 6-Sigma, etc.) - Supporting site development and sustainment of QMS - Establish and maintain customer and internal quality standards. - Support
Save for laterRegister your CV23/04/2024 | Fulltime | Huddersfield | CV-Library | £40,000 - £50,000 / Year Key responsibilities - Measure performance and recommend improvements continually. - Implementation and management of an effective QMS System across the business. - Responsible for developing/implementing procedures for inspecting, testing and evaluating the quality of the business products
Save for laterRegister your CV22/04/2024 | Fulltime | Greater Manchester | CV-Library | £30,000 / Year Phone number removed). Key responsibilities for the Regulatory Affairs Officer (Hybrid working) Ensure Regulatory compliance with drugs imported overseas. Lead any changes within the regulations and ensure the QMS is complaint with these. Review and monitor licence applications to the MHRA. Manage
Save for laterRegister your CV22/04/2024 | Fulltime | Cambridge | CV-Library | £35,000 - £40,000 / Year For a change in their career. The Role • Adherence to the QMS including root cause analysis and communicating with clients on technical matters. • Assistance in maintenance programs for the Departments specific analytical instrumentation and any other analytical equipment used by the Department. Maintenance
Save for laterRegister your CV