03/06/2024 | Fulltime | Waterford | West Pharmaceutical Services Deutschland GmbH & Co. KGBut not limited to product release, raw material analysis, compendia testing. - Prepare and update Control forms, SOIs, and general lab documentation - Prepare trends and technical reports based on data with guidance from lab management - Maintain cGMP and ISO compliance - Support audit preparations and maintain
Save for later03/06/2024 | Fulltime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGTo receive an alert - Please wait. Title Technical Writer - FTC Requisition ID 65847 Date May 31, 2024 Location Dublin, Leinster, IE Department Operations 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 later29/04/2024 | Parttime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGIn improving the manufacturing of product and develop the most optimum molding process and tooling and automation solutions which meet or exceed customer requirements. This person will provide the company with the technical resources to ensure that current and future projects are run in accordance
Save for later22/04/2024 | Fulltime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGWith the technical and quality resources to manage the quality deliverables on selected NPI projects and day to day validation activities and will coordinate the necessary
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 later12/06/2023 | Fulltime | Dublin | West Pharmaceutical Services Deutschland GmbH & Co. KGLed giving program. Job Summary Responsibility for compliance with the Quality and Regulatory requirements for combination medicinal and device products assembled and packed by West CM (Dublin). This role is also responsible for overseeing the compiling of technical and quality documents in support
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