IPQA
Issue batch production record.
Issue and Retrieval of cleaning records.
Review of batch production and equipment cleaning records.
Documentation systems issue and control of documents.
Upkeep of documentation.
Issue of certificates photocopies to the user departments, with draw of obsolete copies and issue of uncontrolled copies whenever required.
Checking the certificate of analysis prepared by quality control.
VALIDATION
Reviewing of equipment qualification & other documents.
Reviewing of Engineering related documents.
Preparation of Risk Assessment
Preparation of validation protocol
Supporting of customer / regulatory audits.
Trending of Manufacturing norms, Quality Parameter, Microbial count Monitoring & Water trend.
Preparation of monthly report.
Review the Change control with impact assessment of all changes.
Preparation of Annual product quality review (APQR).
Upkeep of documentation.
Document/Format Issuance and Retrieval
Preparation of Standard Operating Procedure
📌 Walk In Qa Officer Ipqa/validation/apqr Vellore
🏢 Malladi Drugs u0026 Pharmaceuticals
📍 Vellore
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