CK Group are recruiting for a Regulatory Life CycleManagement Scientist, to join a global Consumer Healthcare companywho are based in Reading, on a contract basis for 12months.
Company:
Out client is a global consumer healthcare business with well knownhousehold brands.
Location:
The role is based in Reading.
Role:
* CoordinateRegulatory Life Cycle Management activities across multiplecountries within and outside Europe.
* Coordinatewith Local Regulatory Affairs for variations, renewals andanswering health authority requests.
* MaintainGlobal Master Dossiers and compile, review, and provide dossiersfor local registration and compliance to achieve variations for thespecific product portfolio.
* Ensure regulatoryassessments are conducted for change controls in the respectiveVeeva Quality Tracking system.
* Ensure that theVeeva Regulatory Information Management system is maintained andupdated for all activities under role responsibility, includingreview of documents.
* Provide strategic inputinto Regional Product labelling and approval to enable commercialactivation of productlaunches.
YourBackground:
* Educated toideally Masters degree level in pharmacy, engineering, chemistry ora similar field.
* Regulatory affairs experiencein OTC medicinal products and experience of lifecycle managementacross EU or wider markets.
* Experience ofdossier maintenance and product change management as well asworking with complex Regulatorydatabases.
* Excellent attention to detail, goodcommunication and presentationskills.
Apply:
It is essential that applicants hold entitlement to work in the UK.Please quote job reference 106651 in allcorrespondence.