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:
1. The role offers hybrid working
2. 37 hours per week with an early finish on Fridays
3. Exceptional hourly rate
4. Great working environment
5. Really friendly team
6. Free products at the discretion of the client
Main Job Responsibilities:
1. General administrative tasks and working with other departments within the business to collate and build technical documentation
2. Handling tasks to support regulatory processes and projects
3. Responsibility for tracking and co-ordinating registration activities and providing support for regulatory submission activities
4. Logging and reporting registration on the in house system
5. The ability to match product names to internal product codes and abbreviations
6. Using Government website to apply for documents and forms
7. Understanding product changes and co-ordinating notifications to distributors
8. Arranging formal signatures on documents and overseeing the Legalisation of documents
9. Uploading registration tasks to the database and maintaining license details
10. Maintaining folders and documents
11. Liaising with distributors, internal departments and governing bodies
Requirements:
1. Any previous experience gained in Cosmetic or Medical Device Regulations/Registration in EMEA desirable
2. Strong administrative experience
3. Good communication skills
4. Excellent attention to detail
5. Multi-tasking and time management skills with the ability to prioritise tasks
6. Self-starter, forward thinker and proactive
7. The ability to work independently on routine activities with minimum day to day supervision
8. 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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