29/04/2024 | Fulltime | Cambridge | CV-LibrarySystem. Job Summary Providing support with administration of the QMS, including non-conformance, root cause analysis and CAPAs. Control of documentation; maintenance of records and use of QMS for document control. Support with internal and external audits. Trending for CAPAs and preparation of quarterly
Save for laterRegister your CV01/05/2024 | Fulltime | Cambridge | CV-Library | £20,000 - £26,000 / Year Policies - Supporting with QMS activities including issuing validation plans and performing risk assessments - Support all departments with writing and assessing change controls, non-conformances, root-cause analysis, risk assessments and CAPAs - Support with internal and external audits and other
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 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 CV30/04/2024 | Fulltime | Cambridge | CV-Library | £50,000 - £60,000 / Year To expand and strengthen their skills, learning from expert colleagues from a variety of technical backgrounds. An excellent salary is on offer. Keywords Quality, QMS, ISO, ISO9001, 8D, PDCA, Continuous Improvement, Lead Auditor Another top job from ECM, the high-tech recruitment experts. Even
Save for laterRegister your CV30/04/2024 | Fulltime | Cambridge | CV-Library | £40,000 - £50,000 / Year Responsibilities - Develop and implement robust Quality Management Systems (QMS) to maintain compliance with ISO standards. - Conduct regular audits and inspections to assess adherence to quality processes and identify areas for improvement. - Collaborate with cross-functional teams to resolve quality issues
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 CV29/04/2024 | Fulltime | Cambridge | CV-LibraryOf their SHE roles and responsibilities in line with National Grids/Cadent/SGN QMS. Undertake reviews of Fastflow/contractor documentation, participate in site safety meetings, H&S Audits & Sensible Monitoring Inspections on gas projects. Provide independent H&S audit capability to the delivery teams
Save for laterRegister your CV17/04/2024 | Fulltime | Cambridge | CV-LibraryAnother key part of the role is the contribution to the Standard Operating Procedures. To be considered for the Validation Engineer you will need to have prior experience with medical devices and an ISO 13485 environment, coupled with expertise in writing test protocols and familiarity with QMS
Save for laterRegister your CV16/04/2024 | Fulltime | Cambridge | CV-LibraryTo the QMS. Ensure the reagents used undergo a robust QC test before being release to development scientists. Track and record QC pass and fail data. Working with stringent SOPs to ensure the wider ream is able to perform environmental monitoring. Work with respect to the ISO 13485 and FDA regulations
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