Do you have experience within the medical field? Have you worked with Medical Devices previously? Would you like to work with cutting edge innovation and state of the art technologies?
Due to continuing strategic growth within our Medical Devices business, we currently have vacancies for Technical Specialists in various departments. This is an excellent opportunity to join a leading Notified Body, driving up the standard of safety and performance of Medical Devices for patients, and to be involved in the evaluation of cutting edge innovation and state of the art technologies.
This is a full-time salaried, home-based role in the United States with some travel (15-25%).
This role offers real diversity and variety, building, controlling and managing a portfolio of Medical Device CE marking schemes focused around your area of expertise. In addition to reviewing and evaluating medical device technical documentation you could also be undertaking Medical Device QMS assessments or advising and mentoring colleagues in your areas of competence. Strong interpersonal communication and project management skills are at the heart of this role as you work on a daily basis with medical device manufacturers as they plan and execute their conformity assessment projects.
To be successful in this role you'll need to apply the significant knowledge and extensive ‘hands on’ experience that you have gained in research, design and development of medical devices, including the application of the principles of design control, risk management and performance or clinical evaluation.
The right candidate will have demonstrated:
The role requires you to have extensive experience in the design, development and manufacturing of Medical Devices which includes one or more of the following technologies:
Do you believe the world deserves excellence?
BSI (British Standards Institution) has over 81,000 clients in 180 countries, and is an organization whose standards inspire excellence across the globe. BSI Medical Devices Notified Body provides rigorous CE and ISO 13485 certification to manufacturers globally. The team apply their knowledge to 3rd party conformity assessment of all types of medical devices; active devices, active implantable devices, in vitro diagnostic devices, orthopaedic and dental devices, vascular devices, wound care devices and many others. The team has doubled in size over the past eight years, demonstrating the company’s desire to succeed and deliver world beating results. There are exciting opportunities for further growth of the Medical Devices team.