Regulatory Affairs Specialist Johnson And Johnson Medtech Orthopaedics
Johnson & Johnson MedTech | Orthopaedics
Leeds, West Yorkshire, United Kingdom
3d onsite
Uk/ire regulatory environment monitoring
Mhra medical device registration
Uk/irl regulatory compliance
This role will involve monitoring of the UK/IRE Regulatory Environment and ensuring local regulatory compliance of products and innovation of processes
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 J&J standard requirements and project timelines are met.
Matching Summary
This role will involve monitoring of the UK/IRE Regulatory Environment and ensuring local regulatory compliance of products and innovation of processes.
Skills & Requirements
Must-have
UK/IRE Regulatory Environment monitoring
MHRA Medical Device Registration
UK/IRL regulatory compliance
Medical device regulatory documentation
Nice-to-have
High degree of initiative
Outstanding collaboration
Communication and negotiation skills
Open minded, listens to others
Customer focused
Well organized, sense for detail
Diplomacy
Key Requirements
Degree in Science or Law
Medical device background
Knowledge of UK Regulation MDD Directive & MDR Regulation