Operator - East London, South Africa - Aspen Pharma Group
Description
Overview
- Operate equipment in the manufacturing and packing of products
- Prepare, clean, and inspect work areas and equipment
- Troubleshoot machines and raise maintenance issues
- Carry out required training and administrative tasks
Operational Support
- Identify gaps in current policies and procedures
- Optimise and facilitate implementation of processes
- Operate equipment as per standards and expected efficiency, and ensure compliance to GMP and SHE standards
Inspections & Verifications
- Perform preproduction checks such as environmental, scale and equipment prechecks as per BMR, SOP and product specifications
- Verify scale and measuring equipment performance
ProductionPreparation**- Ensure availability of materials and equipment for manufacturing
- Perform Type-A and Type B changeovers; Clean and prepare the area and equipment before and after processing
- Prepare solutions for production activities as per SOP
Production Processing
- Clear and feed the manufacturing line
- End of line packing and inspections
- Perform central lining review to establish optimal production settings
Routine Support Tasks
- Clean area and equipment before and after processing of materials
- Perform equipment prechecks and facilitate transfer of equipment
- Sort defected product and dispose of according to procedures
- Provide information to assist with campaign preparation
- Train new Assistants and Operators and transfer of skills
- Operate manufacturing and packaging lines as per requirements
- Resolve minor and assist with major breakdowns/ maintenance
- Perform change overs, settings and minor maintenance as per autonomous maintenance standards
Troubleshooting
- Conduct root cause problem analysis on machines
- Raise maintenance issues with management for resolution
- Perform adjustments and preventative maintenance on machines
Reporting & Record Keeping
- Complete batch record labels and OEE sheets
- Perform halfhourly inspections of production area(s)
- Record manufacturing/ machine down time
- Attend shift meetings
- Perform IPQC or quality inspections per responsible areas
- Provide information for reports; consolidate standard documents
- Maintain and update records and systems as required
Requirements:
Background/experience
- National Certification (N3) with 02 years' related experience
- Manufacturing experience
Specific job skills
- Basic technical knowledge of pharmaceutical production processes, procedures, systems and equipment
- Basic understanding of pharmaceutical standards and compliance requirements
Competencies
- Finalising outputs
- Following procedures
- Taking action
- Information Gathering
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