20/05/2024 | Fulltime | | Hays Specialist Recruitment LimitedHas several vacancies for BMS Services new roleAs a Service Engineer, you would be responsible for servicing and maintaining existing BMS systems and identify and correct any faults or irregularities. In addition, you would be expected to identify and action opportunities for upgrades
Save for later11/05/2024 | Fulltime | | Hays Specialist Recruitment Limited | €50,000 Bespoke engineering systems, and it is essential that you have a willingness to you'll get in returnIn return, the successful candidate will be rewarded with a competitive salary and great benefits package including a generous annual leave, pension, overtime and bonuses. What you need to do
Save for later29/04/2024 | Fulltime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGTo receive an alert - Please wait. Title Senior Quality Engineer Requisition ID 65410 Date May 16, 2024 Location Dublin, Leinster, IE Department Quality Description At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company
Save for later22/04/2024 | Fulltime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGQuality Engineer (NPI) Validation Requisition ID 64441 Date May 7, 2024 Location Dublin, Leinster, IE Department Quality Description At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our
Save for later15/04/2024 | Fulltime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGSupports the business in the management of the technical spare parts program ensuring a functioning spares management system capable of meeting the growing demands of the facility reporting to the Toolroom Supervisor. Essential Duties and Responsibilities - Work with Engineering to accurately produce
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
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