16/01/2024 | Fulltime | Dublin | CV-LibraryIn CSV and/or CQV for laboratory systems and instrumentation - Experience in regulatory audits. - Working knowledge of biologics analytical methods and specifications and Good Manufacturing Practice (GMP). - Strong CSV experience with analytical instrument maintenance - Excellent understanding of data
Save for later13/11/2023 | Fulltime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGRequirements - Must have a third level qualification in Engineering/Quality/Science. - Must have 2+ years work experience in a Medical Device manufacturing environment. - A working knowledge of quality systems such as ISO 13485 is essential. Experience and knowledge of 21 CFR Part 820 and EU GMP
Save for later30/10/2023 | Fulltime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGEuropean cost accounting team located with West’s Financial Services team in Dublin, Ireland. You will be responsible for the accounting across multiple manufacturing sites including the preparation of journal entries and account reconciliations. Essential Duties and Responsibilities - Prepare journal
Save for later12/06/2023 | Fulltime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGOf submissions to the relevant authorities, for obtaining and maintaining the required medicinal product manufacturing authorisations. Reports directly to the Snr. Quality Manager. Essential Duties and Responsibilities - Reporting to the Snr. Quality Manager of West CM (Dublin), this role will be responsible
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