~Responsible for the handling and packaging of Class I and Class II Medical Devices~Operated in a GMP controlled environment, Operating to European regulations ISO 13485 and FDA requirements for 21 CFR part 820~Responsible for the Development and Training of operators to new procedures for the Repack area.~Responsible for fault finding and troubleshooting activities within the relevant area to maximise productivity in a compliant and controlled manner~Responsible for the batch labeling and information inspections associated with the packaging of Class II and Class III medical devices~Responsible for assisting in the completion of IQ/OQ/PQ qualifications within my area, assuring that all products assigned to the area was validated according to the run protocols.~Responsible for leading a team of 12 operators meeting and exceeding required hourly targets ~Responsible for timekeeping and attendance tracking for a team of 12 operators.~Responsible for completing Daily and Weekly PM (Preventative Maintenance) activities within my area on the automated PM system (OPUS)~Responsible for completing all required relevant paperwork in accordance with GDP (Good Documentation Practices) within my area and responsible for final review and sign off in accordance with GDP~Responsible for generation and maintenance of Shift Handover Reports responsible for creation and review of Memos required for process deviationstrained on and required to complete eDHR (electronic Device History Requirements) sign offs for each Batch processed within the area.~Responsible for liaising with Operations Manager/ Quality Team in relation to achieving area targets and priorities in a quality compliant manner.

Production output of Skincare and Cosmetic brands (Hugo Boss, Olay, Max factor)Adapted to line changes for different products and sizeResponsible for chemical waste disposal Contributed to targets in Quality, Quantity and SafetyFirst Aid team member