Are you an experienced QC professional who has worked within a cGMP environment?SRG have a fantastic opportunity to join a successful and expanding organisation in the Central Belt of Scotland.The Role:Development of quality systems, in particular those relating to QC activities of the Quality DepartmentReview and approve data such as Environmental Monitoring and QC testingAssist with stability study management Approve and release incoming Raw MaterialsManagement of QMS for QC investigationsSupport analytical method technical transfer and validationCarry out a range of analysis such as Environmental Monitoring, endotoxin, bioburden, pH and analytical chemistry based methodsSupport the ongoing maintenance and management of subcontract facilitiesTrending QC dataEnsure all QC processes are compliant with cGMP guidanceSkills:Strong communication skillsAble to work well as part of a teamAttention to detailTime management and planningRequirements:Experience in QC release and/or stability testing would be beneficial or experience of similar techniques and lab workExperience of working in a GMP regulated environment would be beneficialExperience of helping manage a QMS and assist with investigationsPlease apply online or contact Emma for more information if you feel you have the relevant skill and experience to be considered for this role.