Job Description

Our client is a well-known pharmaceutical business.

Responsibilities

• Reviewing and providing decisions based on the IQC sheet.
• Handling online feedback to production for correction.
• Creating daily plant rounds to ensure compliance with SOPs, GDP, GMP guidelines, etc. on the shop floor.
• Refer to ZMIC for special instruction during color change/ product change and guide the IQC operator for the same. Reviewing the implementation of the same.
• Monitoring CAPA during shifts.
• Investigating internal incidences/failure to identify the Root cause analysis and take corrective/preventive action for the same.
• Tracking instances of repeat failure from operators and taking measures/set processes to avoid re-occurrence of the same and to ensure FTR.
• Handling operator training and performance monitoring.
• Creating line clearance of camera inspections, HCM, ATS, printing machines, and Final Inspection System.
• Ensuring document verification is generated during shift daily against defined standards.
• Performing challenge test of camera inspection.
• Shading monitoring within the shift.
• Performing complaint sample / material return / free samples analysis and report generation.

Qualifications

• Bachelor's or Master's degree in Engineering.
• At least 8 years of Experience in QC/QA function or related field.
• Experience strong decision-making skills. And have experience in the existing industry.
• English Communicable.