About the Role
We are looking for a biomedical engineer who has the ability to interpret and apply legislative guidelines and analyze technical information to make informed decisions and prepare high-quality regulatory decisions and notices to clients.
Key Responsbilities
- regulatory and technical assessment for medical devices including evaluating data, collating relevant expert advice and preparing clear evidence-based assessment outcomes and statements.
- Managing record keeping with the regulatory requirements
- Providing clear advice and feedback on application assessment requirements and outcomes
To be successful, you will need to be a qualified Biomedical or Mechanical Engineer with a bachelor's and/or master's degree. Ideally 12 months experience working in the medical device sector with some working knowledge of regulatory requirements for a range of devices - Class 1-111. Strong communication skills are essential, with strong technical writing and high attention to detail. This a team orientated environment where you will work closely with a range of stakeholders, and a sense of urgency will be required.
