19/04/2024 | 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 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 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 CV17/04/2024 | Fulltime | Cambridge | CV-Library | £40,000 - £50,000 / Year 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. Ideally this will be from a mechanical engineering background and any experience with CAD would be highly beneficial. For this role, we are ideally
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
Save for laterRegister your CV27/03/2024 | Fulltime | Cambridge | CV-Library | £75,000 - £85,000 / Year We are supporting a leading international manufacturer in their search for a Global QMS Manager. This role will support all sites within the group and be responsible for maintaining robust QMS within a highly regulated sector. As Global QMS Manager, you will take the lead on global initiatives
Save for laterRegister your CV08/04/2024 | Fulltime | Cambridge | CV-Library | £28,000 - £31,000 / Year In? On offer is the opportunity to join a company which is renowned for the development of specialist polymers and a major provider of biocompatible materials for medical applications to the ophthalmic industry. You will be responsible for supporting administration of the QMS, and assisting
Save for laterRegister your CV02/04/2024 | Fulltime | Cambridge | CV-LibraryWill include - Verification and validation tests - Updating QMS system as required - Helping develop SOPs - Working alongside other departments as required. An ideal candidate for the Validation Engineer role will have - Previous experience verifying medical devices within a regulated environment
Save for laterRegister your CV05/04/2024 | Fulltime | Cambridge | CV-Library | £517 - £690 Will help shape their SAP landscape, providing expert guidance on solution design, business process optimization, and ensuring alignment with industry best practices. You will require a deep understanding of SAP S4HANA modules SD, MM, PP, QM, a track record of successful implementations, and the ability
Save for laterRegister your CV25/03/2024 | Fulltime | Cambridge | CV-LibraryAligning test protocols with product requirements; ensuring that ISO 13485 standards are adhered to; implementing test plans and documenting via a QMS; design review procedures based on data analyses. Requirements - Background in engineering (ideally a degree in mechanical or electronics engineering
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