1 to 5 of 5 Temporary QMS Jobs

production of bespoke military vehicles. Day-to-day, you'll be responsible for providing assurance at all levels of the business that the quality management system and associated policies and processes have been effectively implemented. Responsible for maintaining the audit programme including all internal, external and joint audits Produce quality more »

verify if product meets the requirements of Company specifications in line with existing quality system 2. To carry out meat intake inspection, following the QMS procedures. To ensure that all deliveries are to specification and to communicate non-conformances to the QA Team Leader 3. To respond to the needs more »

experience of line managing staff Experience of training and supervising Experience of working in a licensed facility holding an MIA(IMP) Proven experience of QMS management Proven experience of risk management Proven experience of leading investigation and root cause analysis Proven experience of leading internal and/or external audits more »

ina clinical pathology laboratory as a Biomedical Scientist Understanding of health and safety legislation pertaining to clinical laboratories Understand the components of a quality management system Desirable Problem solving ability Understanding of laboratory quality issues Familiar with pathology LIMS Good knowledge of immunological processes in health and disease Qualifications Essential more »

coordinating IMP supply and eventual closure and archiving of the trial To be responsible for ensuring the requirements of the production area's quality management system are maintained and developed as required by the MS(specials), MIA(IMP) licenses and NHS guidance. To deputise for the Senior Production Pharmacist - Clinical … in accordance with data integrity principles to be audit ready at all times. Governance and Quality To ensure that the Clinical Trial Pharmaceutical Quality Management system is maintained and developed in accordance with the MS(Specials) and MIA(IMP) license requirements and in response to changes in regulations and legislation. … quality and final product disposition from a production perspective in liaison with QA and the QP. To support and document change through the Quality Management System to both reduce risk and drive innovation in clinical trial activities and the overall clinical trials service. To ensure all changes to the Quality more »