01/05/2024 | Fulltime | Ballina (Connacht) | TipTopJob Ireland | People leader, with the desire to play a key role in career development? The Role We have an exciting opportunity within our Biologics Division located in Ballina, Co. Mayo, Ireland for a Quality/Regulatory Compliance Manager to join the team on a permanent, fulltime rting to the Senior
Save for later10/05/2024 | Fulltime | Ballina (Connacht) | TipTopJob Ireland | Production Scheduler (12 Month Contract) Department Supply Chain Reporting Relationship Supply Chain Manager SUMMARY The role of the Production Scheduler is critical to the successful development and delivery of the production plan, and therefore to achieving our business goals. They act
Save for later08/05/2024 | Fulltime | Ballina (Connacht) | TipTopJob Ireland | Manufacturing Operations as primary customer. The position will liaise with Global Engineering (GE), New Product Development (NPD), Research and Development (R and D), Quality Assurance(QA) and Supply Chain(SCM) in order to effectively carry out its responsibilities. RESPONSIBILTIES Key responsibilities
Save for later01/05/2024 | Fulltime | Ballina (Connacht) | TipTopJob Ireland | Ireland. This role shall report to the Cell Based Assay Development Manager and the main duties and responsibilities shall be Research and develop new InVitro cellbased methodologies to meet client requirements and/or company strategic objectives. Ensure all new methods are validated in accordance
Save for later01/05/2024 | Fulltime | Ballina (Connacht) | TipTopJob Ireland | And responsibilities shall be to assist the Department Manager and/or the Scientist in the following Leading the execution of routine cellbased potency assays Support technical transfer, qualification and validation of new cellbased assays Maintenance and propagation of antibiotic free cell cultures. Evaluation
Save for later01/05/2024 | Fulltime | Ballina (Connacht) | TipTopJob Ireland | Regulatory compliance, where appropriate. Execution of study plans and - or complex methods in the laboratory for transfer - validation - method development and leading troubleshooting efforts as required. Report - SOP writing and performing necessary updates. Liaise with the Quality Department
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