Quality Assurance Administrator - Benoni at Cipla

Job Purpose

• To ensure safety by ensuring OHS (ACT) Compliance, no fatalities occur on-site, no LTI incidents, and no critical /major findings
• To ensure efficiency by process standardization, developing robust products, capacity creation, and reduction of cycle time
• To ensure quality by obtaining SAHPRA site compliance, QMS /Cipla compliance, maintain RFT process/documents standards, and have no critical/major findings post inspections/ audits
• To ensure the development of current staff, and ensure the staff are performance-driven
• To ensure the overall reduction in site costs with regards to OPEX reduction, waste reduction, ensure RFT batches by reducing OOS, OOT, and deviations, ensure there are no write-offs of batches
• To assist in new product development and/ or technology transfers

Accountabilities

• Quality Management system
• Change management system
• To ensure compliance in shop floor by actively participating in QMS activities.
• To work on Quality Attributes for continuous improvement.
• Risk Assessment
• Root Cause Analysis
• RA / Dossier related queries
• Artwork
• Validation Assistance

Education Qualification

• BSc Degree or National Diploma in Scientific field

Relevant Work Experience

• Minimum 2 years in pharmaceutical manufacturing environment.
• Minimum 2 years of experience in Quality Assurance.
• Knowledge of cGMP, QMS and QA Processes   
• Good communication skills & attention to details
• Supplementary requirement: Software computers: MS Office, Excel and PowerPoint