The Role:Responsible for the coordination of all First Registrations, Renewals, Tenders, Response to questions and Site Registrations submissions. Ensuring delivery to agreed timelines and in...
Provide full support to all registration activities and regulatory submissions throughout the world.
Facilitate worldwide product registration activities by compiling appropriate dossiers, submissions and responses to regulatory bodies.
Maintain information on worldwide regulatory requirements and the status of product registrations.
Liaise with all departments and project teams to co-ordinate timely applications for regulatory approvals.
To be aware of progress and developments of worldwide regulatory requirements.
To follow and promote Company, HS&E and Quality procedures and standards to enable the site to achieve and maintain excellent results.
University level (Life Sciences background is preferred)
Experience within Regulatory Affairs, focussing within Medical Devices
Experience interacting with Health Authorities, LOCs and Global Regulatory Teams.
Strong Project Management Skills.
The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the EU/UK. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency.