Operator - Granulation
Job Description:
- Documentation review and reconciliation. Responsible and ensuring following GMP.
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Granulation Process Management: Oversee all aspects of the granulation process, including equipment setup, operation, and troubleshooting. Ensure that granulation activities are carried out efficiently and in compliance with standard operating procedures (SOPs) and regulatory requirements.
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Team Leadership: Lead and supervise a team of granulation operators, providing guidance, training, and support as needed. Delegate tasks and responsibilities effectively to ensure smooth operations and optimal performance.
- Equipment Maintenance: Coordinate with maintenance personnel to schedule and perform routine maintenance and calibration of granulation equipment. Address equipment issues promptly to minimize downtime and maintain production efficiency.
- Quality Assurance: Monitor granulation processes to ensure product quality and consistency. Conduct regular checks and inspections of granulated materials, verifying adherence to specifications and quality standards. Address any deviations or non-conformities in collaboration with the quality control team.
- Documentation and Record-Keeping: Maintain accurate records of granulation activities, including batch records, equipment logs, and production reports. Ensure that all documentation is completed accurately and in accordance with regulatory requirements.
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Process Improvement: Identify opportunities for process improvements and optimization in granulation operations. Implement changes and initiatives to enhance efficiency, reduce waste, and improve product quality.
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Safety and Compliance: Ensure compliance with safety protocols, Good Manufacturing Practices (GMP), and other regulatory requirements related to granulation operations. Promote a culture of safety awareness and adherence to procedures among team members.
Key Skills :
Company Profile
A modest beginning, while being morally obligated towards improved human health, liquid orals and tablets were manufactured for the local markets. Supported by initial success, other dosage forms such as capsules, dry syrups and ointments were also added. The gradual expansion of the organization was a series of milestones over the years which included exports, building of a separate facility for penicillin antibiotics and a brand new facility for general products, all replete with modern , state of the art and most current cGMP compliant systems.
The latest cGMP norms were always adopted as a habit and culture. A qualified, experienced, continually updated and committed personnel base and our well maintained facilities has enabled us to achieve quality certifications from WHO, UK-MHRA, South Africa-MCC, most other African and European nations.
Our Organization is ISO 9001-2015 certified.
Walk-in Interview Available
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