Responsible for revision, issuance of revised documents and withdrawal of superseded quality documents and obsolete the superseded documents.
Document control (Handling of master documents like standard operating procedures, specification & testing procedures, validation and qualification protocol, reports, batch manufacturing and cleaning records, annual product review reports etc.).
Preparing master list of documents.
Issuance of formats, registers and analytical data sheets.
Review of standard operating procedures related to other departments.
Handling of dispatch related activities.
Handling of Archival System.
Handling of Vendor Qualification.
Handling of Customer Queries.
IPQA rounds to ensure Quality System is followed in facility.
Preparation & review of department SOPs.
Login, handling/Review and approval of QMS documents (CCF, deviation, OOS, CAPA, I...
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