Description
Role: Regulatory Affairs Manager PLPI (Product Licence Parallel Import)Location: London
Salary: Competitive
Responsibilities:
- Require detailed knowledge of the full licence application process for all the different Regulating Bodies and establish contacts/relationships with key people within these bodies.
- Going through all correspondences from the governing boards and logging them in the appropriate databases and looking at the issues raised.
- Involvement in the submission and monitoring of successful pharmaceutical licence applications by liaising with various governing boards to obtain granted licences as soon as possible.
- Maintaining and updating product samples and product files, to ensure applications are done in line with the regulatory requirement and proactive license checking and maintain the compliance
- Regular meetings regarding development
- Continually review the PIL workload with a commercial focus and ensure work is prioritised in a way that will realise cash quickly
- Take initiative to stay up-to-date of commercial changes by reading widely and seeking out applicable knowledge that may affect the way we work.
- Previous experience in a similar role
- Excellent people management skills
- Has good communication skills both written and verbal
- Must computer literate and competent in MS Office.
- Ability to keep up-to-date with Pharmaceutical trends and developments within the industry.
If the above job description is something you would consider then please do get in contact with me. (Referring a friend or an ex colleague is also something we reward here at Real).
Please send a copy of your CV to L.khan(a)realstaffing.com alternatively you can call me on .