You will carry out all duties and responsibilities in accordance with requirements of the Health and Safety at Work Act, relevant statutory requirements approved codes of conduct and local policies and procedures with particular regard to personal safety and that of colleagues in the workshop. You will need to produce written information associated with the equipment produced e/g/ user instructions in line with the legislation associated with the manufacture of medical devices. Another important element of the role is to teach and train other members of CCAS and Healthcare Science staff on aspects of design development and manufacture of assistive technology. You will need to work independently to provide clinical engineering lead to multidisciplinary teams dealing with complex and highly specialist caseloads.
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