Your new role
- Compile and submit a registration dossier for both pharmaceutical and medical pharmaceuticals to local authorities, and obtain regulatory approvals in a timely manner.
- Update and maintain various RA databases to keep up-to-date portfolio management.
- Interaction with local regulatory authorities, as well as inter-department coordination
- Support tender submission and manage change for both pharmaceutical and medical device products.
- Responsible for advertising or promotional material review and obtaining associated regulatory approval if required
- Provide professional advice on regulatory strategy and prepare a submission plan to support business;
- Be the mentor of a junior RA colleague.
What you'll need to succeed
- Bachelor’s Degree or above.
- Good command of written and oral English.
- Good communication skills; detail-oriented, well-organised and good team player.
- With minimum of 5 years’ work experience of regulatory / quality in the medical device or pharmaceutical industry.
- Sound basis of regulatory / quality knowledge and strong project management skills.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.