Joe Murphy Email & Phone Number

Experienced in Quality Assurance and Manufacturing management with demonstrated experience within the Medical Device industry complying with ISO 13485 and ISO 9001. Key areas of experience are:- Root cause analysis utilising lean techniques. - CAPA progression, support and management. - Non-Conformance management. - Complaint investigation and management. - Risk management including FMEA. - Notified Body and Customer audit support, including experience as back room lead and audit host support. - Supporting eQMS implementation and QMS management.- Procedure/Process implementation, review and management. - Change control. - Supporting new product development including design control. - Data analysis and trend reporting. - Process improvement. - Team management including appraisal and SMART objective setting. - NVQ Level 2 in Team Leading. - Safety management including risk assessment, COSHH and safety auditing.