28/05/2024 | Fulltime | Limerick | CV-Library | €43,162 - €51,794 / Year Agreements and respond to emergency breakdowns promptly Specify and order necessary materials, maintaining stock levels of critical spares Provide technical support to the on-site team and client, ensuring compliance with ISO 17025 Lab Accreditation Ensure all maintenance paperwork and procedures
Save for later09/05/2024 | Fulltime | Limerick | CV-LibraryAnd materials management. - Maintains regulatory compliance in accordance with current Good Manufacturing Practices (cGMP). - Collaborates with Cross functional teams to resolve issues, complete investigations and maintain compliance. - Responsible for review and approval of the following types of documents
Save for later07/05/2024 | Fulltime | Limerick | CV-Library | €35 - €60 / Hour Of designs Risk analysis & management Process development engineering Introduce new equipment, materials & technologiesRequirements Mechanical engineering, Material Science, Biomedical Engineering or equivalent degree Experience working as an R&D Engineer on medical device products Understanding regulatory
Save for later27/02/2024 | Fulltime | Limerick | CV-LibraryRequirements · Bachelor's, Master's, or Ph.D. in Biomedical Engineering, Materials Science, Chemistry, or a related field. · Min 2-3 years’ experience in the design & development of Class III medical devices, including familiarity with medical device regulations, and relevant standards (e.g., ISO 13485
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