Overview
Document management of the plant quality system.
Manage the training.
Manage the archive.
Responsibilities
* Provide the initial training in GMP so that new staff can have adequate knowledge about pharmaceutical quality regulations.
* Issue and review the curriculum (training requirements per position).
* Manage the document system (SharePoint).
* Manage the training.
* Manage the archive.
* Approval, review, and closure of the logbook.
* Collaborate with plant personnel in document management, archiving, translation, issuing, and scanning of documents.
* Manage equipment user records.
* “QA” approval of the standard working procedures (SOP) to guarantee the integrity of the data.
* Quality documents implementation: SOPs, Monographies, Analytical methods, Specifications, Sampling instructions, MBR, etc.
* Manage GMP documents, distribution of controlled copies, and removal of obsolete copies.
Qualifications
Knowledge of Microsoft Office.
Basic English.
Previous experience in general administration.
Strong organizational skills.
Ability to manage multiple tasks.
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