Associate I Labeling Operations null

The LOM, Associate I will provide operational support for project tasks including:

• Generate necessary renditions in GDMS (e.g., clean and marked PDF, clean and marked MS Word) and bookmark renditions as appropriate.
• Facilitate workflow through corporate document repository, e.g., 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, and notify internal stakeholders of its availability (e.g., 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.

Education Qualifications:

• Bachelor’s degree required preferably in a science or life sciences related degree.
• 0-2 years of practical experience
   

Experience and Attributes:

• Excellent written and verbal communication skills are essential.
• Complete fluency in the English Language.
• Proven strength in logical, analytical, and writing ability essential.