Job
Description
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, 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 practical experience
Experience and Attributes:
- Excellent written and verbal communication skills essential.
- Complete fluency in English Language.
- Proven strength in logical, analytical and writing ability essential.
Interpersonal and communication skills:
- Clear and effective written and verbal communication skills.
Technical Skills
- High attention to detail.
Systems and Document compilation skills, including:
- Must have excellent computer skills and be proficient with Microsoft Word and similar applications.