Sterile Services Supervisor
To provide full reprocessing of these medical devices using the knowledge and skills gained through training and experience to ensure devices are processed to an agreed specification in accordance with department procedures relevant quality standards and current European legislation (Medical Devices Directive 93/42/EEC Annexe 12 and ISO 13485:2003)
To mentor and encourage the development of less experienced members of staff to ensure consistency of product throughout the department
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