jamjoom pharma jobs in Cairo

Jamjoom Pharma has in a very short span of time emerged, as one of the leading pharmaceutical companies in the Afrasia region. The geographical focus of the company is on countries in the Middle East, Africa, and CIS regions. Strategic focus on selected therapeutic categories has contributed to the rapid growth, market acceptance, and overall success of the company.

Role Summary:

Maintain the cGMP in the workplace, ensure the compliance of activity in relation with written procedures, and provide guidance and assistance to the supervisors, executives, operators, and worker.

Prepare daily reports of work force, productivity, and machine utilization and maintain a high-quality cGMP and safety for internal and external audit.

Responsibilities:

• Responsible for meeting the production targets of semisolid area.
• Responsible for reviewing and analyzing the real time data and initiating the next target condition to fulfil the business targets.
• Plan and organize the monthly production schedule based on the sale projection given by Production manager.
• To coordinate with purchase for the supply of materials in time to have sufficient stock in the stores as per the production plan of semisolid manufacturing area.
• To maintain the factory timings in semisolid manufacturing area.
• To ensure to meet the scheduled product delivery time in semisolid area.
• To identify and prepare list of budgeted items/equipment required in semisolid area.
• To carry out the any other functions allotted by the Production manager.
• To minimize the breakdowns and to improve the machine utilization time in semisolid area.
• To plan of preventive maintenance schedules for the production equipment with the maintenance department in semisolid area.
• Create schedules for employees to ensure optimum staffing levels in semisolid area
• To ensure the discipline and efficiency of production staff in semisolid area is maintained at all levels at all the time.
• To follow the factory discipline.
• Manage and evaluate machine resources to ensure productivity and minimal downtime in semisolid area
• Responsible for delivering the quality product.
• To maintain quality of products.
• To maintain the safety standards during the work.
• To maintain the cGMP in the workplace.
• To implement cGMP in production and ensure the cleanliness of the factory premises.
• To ensure the compliance with the written procedures /work instructions.
• To obey the company policy.
• To maintain good house- keeping standards in the workplace.
• To investigate the market complaints and reports.
• To maintain necessary records related to production, drug control, costing and statutory requirements.
• To maintain the premises in good condition.
• Leads the semisolid area department.
• To provide training, guidance, and assistance to subordinates.
• To ensure smooth inter-departmental coordination.
• Build harmony and morale among the different production units for the orderly production, packing and delivery of quality products
• To organize training sessions and refreshers for subordinates

Qualifications:

• B.Sc. degree in Pharmacy.
• Training / Certificate / studies in GMP “Good Manufacturing practices” or equivalent.
• Not less than 8 Years of experience in pharmaceutical manufacturing.
• Extensive knowledge of Materials, Equipment & semisolid manufacturing.
• Excellent Communication & leadership skills.
• Logical thinker & problem solver with a high degree of attention to details.
• Strong motivation and team management skills