Job overview
To provide technical and clinical input to Prosthetic & Orthotic Services at West Midlands Rehabilitation Centre and the Prosthetic Satellite Clinics in the West Midlands Region.
Within the field of prosthetics and orthotics assess and oversee manufacture of equipment adaptations and modifications including the technical, clinical and therapeutic value of any equipment.
Monitor the activities of of prostheses and orthoses repair, maintenance, modification and supply services, many of which are contracted. Responsible for repair and maintenance service performance and compliance with relevant standards and legislation.
Contribute to the development of an ISO13485:2016 quality system within the West Midlands Rehabilitation Centre.
Main duties of the job
Technical Support to Specialist Orthotics and Amputee Rehabilitation (SOAR)
- Work closely with the Multidisciplinary Team and Prosthetists/Orthotists, regarding the technical selection/prescription of the appropriate device. Ensuring that the outcomes are in line with manufacturers’ specifications, advising on and participating in risk management regarding combination and modification of devices / components.
- In conjunction with Prosthetists and/or Orthotists, assist technically in the quantitative assessment of the user, for the provision of prosthetic and/or orthotic devices.
- Demonstrates tact, diplomacy, and empathy in all clinical interactions, ensuring the holistic needs of patients are considered at all times. Balances patient needs and expectations with service performance and financial constraints, using negotiation and influencing skills to achieve positive outcomes, especially when the situation is difficult for the service user.
- Supervise technical adjustments, adaptations, and repairs to prosthetic and orthotic devices, ensuring compliance with manufacturer specifications, technical standards, and safety legislation. Where hybrid systems (combinations) or modifications / adaptations are prescribed to meet patient clinical need ensure quality management procedures are followed to ensure compliance with medical device legislation.
Detailed job description and main responsibilities
For further details on the main responsibilities, please see the attached job description and person specification.