6-month Temporary role Cheshire based Full time working Monday to Friday Main Purpose: To implement and maintain the Quality Management Systems for MDI Pharmaceutical operations at the site to meet the requirements of cGMP and customer and regulatory audits requirements. To prepare batch and support services documentation files for QP review and verify for the release of medical products prior to shipment. Roles and Responsibilities: Support and administer the Quality Management System to ensure compliance with appropriate QA standards are maintained. Manage appropriate documentation management systems for the MDI business to ensure compliance with the required standards. Identify improvements to Quality Management System and ensure that improvements targets are met, that system changes are implemented, and that such modifications are completed in full compliance with appropriate standards. Compile, review, and prepare batch and support services documentation for QP to release. Support customer/regulatory audits as required and provide QA representation or advice as and when required. Devise, deliver and (where necessary) validate appropriate training packages. Develop an understanding of all appropriate business QA standards and requirements, so that Business'' competency as a quality supplier is maintained and improved. Qualification and Experience: Minimum: HNC in science related subject. Working with and developing Pharmaceutical GMP and quality management ..... full job details .....