Essential
• A natural tendency to lead, facilitate and integrate other disciplines and team members.
• A background in Science or Engineering with a good degree qualification.
• Track record of technically leading medical device development projects through the full development cycle, taking responsibility for quality, time and cost.
• Good experience of healthcare industry-specific regulatory processes, such as: ISO 13485, 21CFR820, and ISO14971.
• A highly structured and methodical mindset.
• Excellent communicator, both verbal and written.
• Confident in presenting ideas and results in a compelling way.
• Comfortable with ambiguity when problem solving.
Desirable
• Commercial awareness for one or more areas within the healthcare industry
• Experience in the project management of large complex development projects
• Knowledge and experience of industry recognised MBSE software tools (e.g. Enterprise Architect, MagicDraw, Rhapsody, Capella, Polarion, Doors, Jama, etc)
• Experience in the use of formal Systems Engineering modelling languages (e.g. SysMl, Capella)
• Formal System Engineering degree or certification (e.g. CSEP, ESEP, Msc, PhD, etc)