Semi- Solid Jr. Manager
5 days ago
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.
**Responsibilities**:
- He/ She will supervise production activities in production departments mainly semi-solid.
- He/ She will lead team in his/her department to achieve objectives.
- He/ She will lead day to day work.
- He/ She will be responsible for documentation
- He/ She will Plan and organize the monthly production schedule based on the sale projection given by marketing department with Production manager.
- He/ She will coordinate with purchase for the supply of materials in time to have sufficient stock in the stores as per the production plan of manufacturing department.
- He/ She will maintain the factory timings in manufacturing department.
- He/ She will meet the scheduled product delivery time in manufacturing department.
- He/ She will identify and prepare list of budgeted items/equipment required in manufacturing department.
- He/ She will carry out the any other functions allotted by the Production manager.
- He/ She will minimize the breakdowns and to improve the machine utilization time in manufacturing department.
- He/ She will plan of preventive maintenance schedules for the production equipment with the maintenance department in manufacturing department.
- He/ She will ensure the discipline and efficiency of production staff in manufacturing department is maintained at all levels at all the time.
- He/ She will Manage and evaluate machine resources to ensure productivity and mínimal downtime in sterile eye drops manufacturing area.
**Qualifications**:
- 5-10 years’ experience in the semisolid production in pharmaceutical companies.
- B.Sc. Of pharmacy is a must.
- Excellent command of English.
- Proficient computer skills including MS Office Applications, SAP.
- Six sigma diploma / TQM is preferred.
- Free governmental obligations.
- Excellent leadership skills.
- Full awareness of cGMP and other pharmaceutical manufacturing guidelines.
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