Generate necessary renditions in GDMS (eg, clean and marked PDF, clean and marked MS Word) and bookmark renditions as appropriate.
Facilitate workflow through corporate document repository, eg, GDMS.
Finalize documents post QC (including update of GDMS document properties such as entry of PfLEET2 number, update of document title, update CDS cover page etc.).
Manage the document status in GDMS and notify internal stakeholders of the availability of labeling documents.
Order SPL for USPIs, check and upload to GDMS upon receipt, notify internal stakeholders of its availability (eg, Regulatory, Drug Listing).
Responsible for ensuring compliance to Company s submission standards, policies and procedures. Ensure all actions taken within role follow applicable SOPs and associated documents so that high quality delivery of outputs and compliance is maintained.
