Regulatory Life Cycle Management Scientist
Posted 22/08/2024 by CK Group- Science, Clinical and Technical
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.
- 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 (phone number removed) in all correspondence.
- Type:
- Contract
- Start Date:
- 21/08/2024
- Contract Length:
- 12 months
- Contact Name:
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- Telephone:
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- Job Reference:
- V-106651
- Job ID:
- 222206954
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