- fulfill all exportation documentation requirements issued by the R&D, as follows:
- MSDS
- Composition sheets
- Declaration letters
- Other related documents requested
- Handle all SASO compliance-related issues for all artworks, i.e. both the current products and new products. Revision of new SASO-compliant claims
- Handle all artwork related requirements for export; Prepare & Revise all new INCI ingredient lists (both English and Arabic).
- Registration document compilation and submission for all new products to be registered in Egypt and/or other countries.
- Revision of PIFs.
- Revision and submission of re-registration files for MOH Egypt registration.
- Follow-up with Regulatory Affairs Representative and/or NPD, registration/re-registration of products/artwork approvals, etc.
- Create regulatory standard operating procedure as necessary
- Develop and maintain database.
- Document, track and store regulatory documents properly.
Education: BSc. in Pharmacy with graduation grade Good and above.Language: Excellent English Language proficiency.Computer: Proficiency in MS Office: Word, Excel and PowerPoint.Years of Experience: From 1-5 years of experience within the area of Cosmetics /Pharmaceutical Regulatory Affairs field.