Our client, a leading regulated manufacturing company are looking for a Quality Manager to join their team. This is an opportunity to join an established company in a challenging and rewarding role with excellent opportunities for personal development. The Role: To manage the compliance within the dept. and ensure that the area is operating in accordance to GLP. To provide support on any external investigations. To lead continuous improvement activities and support projects. Assist in any validation activities that may as the Quality representative within the project. To oversee the product and process performance using appropriate metrics Quality representative on the sign off of change controls, documentation and validation activities. Lead projects for the introduction of new equipment within the site, ensuring that the correct level of validation is completed, that the relevant procedures are updated, and that there is a training plan in place. To approve all reports generated due to any investigational work that is requested due to a complaint or a potential issue within the manufacturing site. To ensure that the data generated is accurate and generated in a timely manner to help close out issues and potentially release product. To ensure that the procedures are up to date and in compliance to the global systems. To ensure that the records generated are accurate and completed in real time. To review method validation protocols and reports on new/ existing test methods, as required. To approve all reports generated due to any investigational work that is requested due to a complaint or a potential issue within the manufacturing site. To ensure that the data generated is accurate and generated in a timely manner to help close out issues and potentially release product. The Person: Experience of scientific report writing including such documents, protocols, deviations, reports etc. Have managed a QA department for 5 years in Pharmaceuticals. Ability to evaluate and assess information to determine appropriate and required actions is critical. Good knowledge of Tablet manufacturing desirable. Knowledge of purified water and Environmental Monitoring systems. Full understanding of the requirements of the Regulatory Standards. Degree in chemistry, science or related technical discipline. Hartley People Recruitment work to the highest ethical standards within our industry and we value the trust that you place in us when you send your CV. We can provide a full consultation in confidence and we guarantee that your CV will not be sent to any of our clients without your prior consent. For immediate consideration please call Pairic on 051-878813 or email your CV in response to this job posting. Hartley People also recruit for similar roles such as Analytical Chemist, Quality Control Manager, Quality Control Technician, Quality Assurance Technician, New Product Development Manger, Quality Systems Manager, Formulation Scientist, Development Technologist.
Waterford, Tipperary, Wexford
101 days ago