hiring for DRA – Labeling
Work location: Hyderabad
Experience: 4-6 Years
1. Responsible for preparation and submission of CBE 0 labelling supplements for approved products to US FDA
2. Responsible for eCTD submission, publication and product life cycle management
3 Draft preparation of text matter for artworks/Labels. Review and approval of artworks, change controls and updating for all regulatory submissions.
4. Initiation of change control regarding Artwork.
5. Compilation of eCTD modules and SPL publication to USFDA
6. Approval of artworks in software & print proofs.
7. Preparation, review and submission of customer import listing SPLs
Interested in relevant can drop a CV to firstname.lastname@example.org