Description
The role's duties include:- Prepares, edits, files, assembles documentation such as reports or technical documents, records, or correspondence.
- Maintains numerical, alphabetical, chronological and/or subject filing system.
- Responsible for file maintenance and record keeping; locates and removes file material upon request.
2-5 Years of experience under FDA regulated environment (such as GMP experience in Pharma industry.)
Please be in contact as soon as possible for this urgent position.
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