Job Description

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 fodders 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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