Regulatory Affairs Specialist Johnson And Johnson Medtech Orthopaedics
Johnson & Johnson Medtech | Orthopaedics
Leeds, United Kingdom
3d onsite
Uk/ire regulatory environment monitoring
Mhra registration of medical devices
Uk/irl impact assessments
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 registration of Medical Devices
UK/IRL impact assessments
Medical device regulatory documentation
Fluent in English
Nice-to-have
High degree of initiative
Outstanding collaboration
Communication and negotiation skills
Open minded, listens to others
Customer focused
At ease in an international environment
Key Requirements
Degree in Science, Law preferred
Medical device background
Knowledge of UK Regulation MDD Directive & MDR Regulation