Summary
Avalon Pharma is hiring a Research and Development Documentation Officer in Riyadh. The role handles regulatory requirements for local, GCC, private-label and MENA markets, including compiling CTD dossiers and preparing registration, renewal and variation documents. Duties also include submitting cosmetic product registrations through e-Cosma, reviewing artwork and DMFs, arranging samples, and coordinating document collection with internal teams and suppliers. Applicants should have a bachelor's degree in pharmacy, chemistry or a related science, and 0–2+ years of experience in documentation and pharmacy registration; a master's degree is a plus.
The posting
As published on avalon.com.sa. Pulled from the employer's site and shown as they wrote it.
To be responsible for revising, developing, & implementing quality procedures & policies to facilitate regulatory compliance as the company enters product development.
Rsponsibilities:
1- Handling Regulatory requirements for the Emerging Markets for LOCAL, GCC,Private label and MENA markets.
2- Compiling of CTD during development, registration, and product lifecycle.
3- Preparing and reviewing variation documents to be filed to respective Body of Health.
4- Preparing and submitting new registration for Cosmetic products (e-Cosma) for Saudi markets
5- Reviewing of Artworks Mockup for new submission, renewal and variation in compliance with existing regulations.
6- Reviewing DMF and following up with supplier for any query related to Body of Health.
7- Arranging samples for SFDA and export registration.
8- Coordinating actively with R&D, Production and QA department for documents collection.
9- Managing CDA agreement with the supplier.
Education: Bachelor’s degree in Pharmacy/ Chemistry/ related science degree / Master’s degree is a plus.
Experience: 0 - 2+ years’ experience in documentation and pharmacy registration.