Manager Production Sterile Manufacturing Area

2 days ago


Jeddah, Saudi Arabia Jamjoom pharma Full time

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**:
Production Manager have wide remit in supervising the manufacturing processes, using your extensive knowledge of the area. This covers such aspects as capacity management, quality, costs, personnel, safety, logistics and maintenance, ensuring that the processes are running efficiently and are safe. Your specific technical expertise may be called on, when necessary, for example in the design and controls of the production systems. As production needs to be completed on time and within budget.

**Responsibilities**:

- Manages the Production (Manufacturing and packaging) of Sterile Dosage forms (Eye Drops, injectables & Blow Fill Seal technology.
- Manage and supervise the daily activities of sterile production lines.
- Executes the weekly plan as scheduled and assists in future planning activities like MPS (Monthly Production schedule) and ensure that the schedule is met.
- Checking all the manufacturing documents on daily basis before packaging and
- reconciliation in SAP on daily basis for all manufacturing activity in the area.
- Co-ordinates with the QA, QC, Engineering, Supply chain departments for day-to day coordination to run the operations. Suggest procedures and policies to improve inter-departmental coordination.
- Ensure the compliance of environment, health, Safety and Hygiene Practices in responsibilities.
- Identifying and complete training program of the existing and new employees. Developing multi-task force in-order to cater the challenging requirements.
- Strict compliance to the procedures and policies, to comply with the cGMP and Quality requirements.
- Monitor the compliance of the procedures and ways to improve the process / documentation
- Identification of the documents requirements of the area and create / revise them in accordance with current requirements (such as BMR, BPR, Recipe, Standards and SOP’s)
- Provide the input for daily/ monthly/ quarterly reports
- Providing input and resources for successful execution of trials, exhibit, scale up batches in coordination with R&D, also identify products and coordinate with R&D for product life cycle management.
- Suggest measure to control the wastage / rejections in the process. Identify Lean Projects for the team for the continual Improvement of the Manufacturing Processes.
- Keeping track of Staff performance (quarterly, half yearly and annually).
- Keep close eye on the staff attendance and conduct counseling sessions, when needed.
- Willing to take more responsibilities / assignments / projects as and when assigned.

**Qualifications**:

- Minimum 4 - 6 years of work experience on managerial position in preferably same filed.
- D. Pharm / B. Pharm / B.Sc. / M.Sc. Biological Sciences.
- Good Computer (MS Office) Skills.
- Good communication and time management skills
- Fluency in Arabic & English languages.
- Having Experience of Sterile Dosage manufacturing and Packaging.
- Result Oriented, having positive attitude and can work with a big team (team player).
- Manufacturing Techniques of sterile product manufacturing (aseptic Process) and BFS technology.
- Production Management in general and aseptic area.
- Knowledge of the Validation procedures of Sterile Area / Products.



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