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You will be updated with latest job alerts via email InProcess Quality Monitoring: Conduct realtime IPQA checks in granulation compression coating and packaging areas to ensure product quality.
Process Validation & Sampling: Perform inprocess sampling environmental monitoring and validation activities to ensure regulatory compliance.
Batch Record Review: Verify Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) to ensure compliance with GMP and data integrity guidelines.
Deviation & CAPA Handling: Identify and report deviations nonconformances and outofspecification (OOS) results assisting in root cause analysis and CAPA implementation.
Regulatory Compliance & Audit Readiness: Ensure compliance with USFDA MHRA WHO and EUGMP guidelines and assist in regulatory audits and inspections.
GMP Compliance & Documentation: Maintain accurate IPQA records logbooks and quality documentation as per regulatory requirements.
Training & Coordination: Work closely with Production QC and Engineering teams ensuring adherence to SOPs and training operators on quality procedures.
Required Experience:
Unclear Seniority
Full-Time