Regulatory Affairs Specialist Johnson And Johnson Medtech Orthopaedics
Johnson & Johnson Medtech | Orthopaedics
Leeds, United Kingdom
Hybrid (3 days in office, 2 days remote)
Uk/ire regulatory environment monitoring
Mhra medical device registration
Uk mdr and eu mdr knowledge
Johnson & Johnson Medtech is seeking a Regulatory Affairs Specialist for its UK/IRE team based in Leeds. The role involves ensuring regulatory compliance for medical devices and includes responsibilities such as registering medical products and conducting impact assessments in line with UK regulations
Job Summary
This role will involve monitoring of the UK/IRE Regulatory Environment and ensuring local regulatory compliance of products and innovation of processes.
Key responsibilities include monitoring of and execution according to local regulatory requirements and advising appropriate partners.
Ensuring that the company's products comply with relevant legislation and standards to be placed on the market in the UK/IRE.
Matching Summary
Match Score: 85
Johnson & Johnson Medtech is seeking a Regulatory Affairs Specialist for its UK/IRE team based in Leeds. The role involves ensuring regulatory compliance for medical devices and includes responsibilities such as registering medical products and conducting impact assessments in line with UK regulations.