13/11/2023 | 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 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
Save for later