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Job Description
- Plan, coordinate, and supervise solid, semi-solid dosage production activities to meet quality, quantity, and efficiency targets.
- Monitor and ensure compliance with GMP, SOPs, safety standards, and regulatory guidelines.
- Review batch manufacturing records and process documentation for accuracy and completeness.
- Coordinate with QA/QC, R&D, Maintenance, and Warehouse teams to ensure smooth operations.
- Identify areas for process improvement and implement initiatives to increase productivity and reduce waste.
- Train and mentor production staff to ensure skill development and adherence to standard procedures.
- Manage resources, including manpower, machines, and materials, effectively.
Job Requirements
- Bachelor’s degree in Pharmaceutical Science is a Must.
- Min 10 years experience in Solid, Semi-solid dosage form production (preparation techniques, compression problems and solutions) with at least 3 years in a supervisory or managerial role in a well-reputed Pharma company.
- Strong knowledge of cGMP, production planning
- Strong background in Lean manufacturing and process improvement tools is a Must.
- Excellent communication and leadership skills.
- Problem-solving and decision-making skills.
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