CK Group are recruiting for a Regulatory Life Cycle Management Scientist, to join a global Consumer Healthcare company who are based in Reading, on a contract basis for 12 months.
Company: Out client is a global consumer healthcare business with well known household brands.
Location: The role is based in Reading.
Role:- Coordinate Regulatory Life Cycle Management activities across multiple countries within and outside Europe.
- Coordinate with Local Regulatory Affairs for variations, renewals and answering health authority requests.
- Maintain Global Master Dossiers and compile, review, and provide dossiers for local registration and compliance to achieve variations for the specific product portfolio.
- Ensure regulatory assessments are conducted for change controls in the respective Veeva Quality Tracking system.
- Ensure that the Veeva Regulatory Information Management system is maintained and updated for all activities under role responsibility, including review of documents.
- Provide strategic input into Regional Product labelling and approval to enable commercial activation of product launches.
Your Background:- Educated to ideally Masters degree level in pharmacy, engineering, chemistry or a similar field.
- Regulatory affairs experience in OTC medicinal products and experience of lifecycle management across EU or wider markets.
- Experience of dossier maintenance and product change management as well as working with complex Regulatory databases.
- Excellent attention to detail, good communication and presentation skills.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 106651 in all correspondence.