Job Responsibilities:
Maintain and manage QA documentation as per company SOPs and GMP requirements.
Prepare, review, and maintain Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).
Maintain SOPs, specifications, protocols, reports, and other QA documents.
Ensure proper documentation, record keeping, and document control.
Review batch records and ensure compliance with approved procedures.
Handle document issuance, revision, retrieval, and archival.
Maintain QA registers and records.
Support deviation, CAPA, change control, and incident documentation.
Ensure documentation is accurate, complete, and compliant with regulatory requirements.
Coordinate with Production, QC, and other departments for QA documentation-related activities.
Assist during internal and external audits and ensure required documents are readily available.