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Document Coordinator
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Full-time
- Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world.
- Maintain the document management system as required including management of templates, allocation of document numbers and review of draft documents.
- Support the revision and creation of GMP documentation through the document change process.
- This includes, but is not limited to, performing routing, document processing, and formatting of documents.
- Perform all routine activities associated with manufacturing batch record issuance and reconciliation as well as creation, issuance and reconciliation of worksheets and logbooks which will require work inside classified manufacturing areas.
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