Job Information

A great opportunity which is being presented on a long term rolling contract basis (with no end date in sight) for a Regulatory Associate with a key manufacturing client in the area.

Package Highlights:
The role offers hybrid working
37 hours per week with an early finish on Fridays
Exceptional hourly rate
Great working environment
Really friendly team
Free products at the discretion of the client

Main Job Responsibilities:
General administrative tasks and working with other departments within the business to collate and build technical documentation
Handling tasks to support regulatory processes and projects
Responsibility for tracking and co-ordinating registration activities and providing support for regulatory submission activities
Logging and reporting registration on the in house system
The ability to match product names to internal product codes and abbreviations
Using Government website to apply for documents and forms
Understanding product changes and co-ordinating notifications to distributors
Arranging formal signatures on documents and overseeing the Legalisation of documents
Uploading registration tasks to the database and maintaining license details
Maintaining folders and documents
Liaising with distributors, internal departments and governing bodies

Requirements:
Any previous experience gained in Cosmetic or Medical Device Regulations/Registration in EMEA desirable
Strong administrative experience
Good communication skills
Excellent attention to detail
Multi-tasking and time management skills with the ability to prioritise tasks
Self-starter, forward thinker and proactive
The ability to work independently on routine activities with minimum day to day supervision
Good IT skills including MS Office – demonstrated capability with Word document processing Excel spreadsheets, MS Teams and Sharepoint

If you have the experience we are seeking and would like to be considered, please email an up to date CV asap.



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