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.