22/03/2024 | Fulltime | Dublin | CV-LibraryAsset structure/ hierarchy reflects drawings and in field conditions. · Data Mapping of current Maximo system to new version. · Development of training plan and delivery of training for end users. · Update and creation of SOP’s, training materials and other quality documentation. · Ensure compliance
Save for later21/03/2024 | Fulltime | Dublin | CV-LibraryEngineers. · Writing reports, documentation, and work instructions. · Training maintenance and operative staff where appropriate. · Attend Software Factory Acceptance and Site Acceptance Testing. · Maintaining and developing change control systems. Qualifications & Experience · Bachelors Degree
Save for later05/03/2024 | Fulltime | Dublin | CV-LibraryContractor documentation, • Lead review of Annual Product Quality Review reports, as necessary. Edit, and negotiate improvements to contractor supplied Annual Product Quality Review reports. • Draft or review, negotiate with contractors, and recommend approval for Quality Agreements Required Qualification(s
Save for later01/03/2024 | Fulltime | Dublin | CV-Library· Prepare contract documentation, specifications, and drawings. · Ensure alignment with project requirements and industry standards. Requirements · Bachelor's Degree in Engineering or Relevant Experience · Typically, 3+ years engineering experience, preferably within a GMP manufacturing environment
Save for later18/03/2024 | Fulltime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGMaterials, finished products and supporting documentation in line with documentation procedures. Requirements - Must have excellent Housekeeping and EHS (Environmental, Health & Safety) standards and a high attention to detail. - Must have a minimum of 1-2 year’s previous experience of working
Save for later16/02/2024 | Fulltime | Dublin | CV-LibraryAnd project processes and procedures and prepare Monthly Environment Reports and KPI’s. - Review environmental management documentation (Construction Environment Management Plans (CEMP), Waste Management Plans, Environmental Work Method Statements (EWMS), consistency assessments etc.) to ensure compliance
Save for later16/02/2024 | Fulltime | Dublin | CV-LibraryAnd internal policies. - Perform risk assessments and impact analyses to identify critical system functionalities and potential vulnerabilities. - Create and maintain validation documentation, such as validation plans, test scripts, traceability matrices, and validation summary reports. - Conduct periodic
Save for later17/01/2024 | Fulltime | Dublin | CV-LibraryThe laboratory. - Performing microbial identifications using MALDI-TOF and MicroSEQ. - Completing all laboratory documentation in a timely and accurate manner. - Compliance with Standard Operating Procedures and Registered Specifications. - Assisting in authoring and reviewing documentation, including SOPs
Save for later20/10/2022 | Parttime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGTo the Product Group Leader this role is responsible for the production of components that meet or exceed pre-determined specifications. Responsible for inspection, packaging, labelling and completion of documentation necessary to provide quality, production and traceability records in accordance with Quality
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