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Job Description
Job Purpose
To supervise, execute and monitor the activities within the value stream to ensure reliable and optimal operation of processes, equipment, utility and facility to achieve target production levels within the framework of current Good Manufacturing Practice (cGMP), quality, safety, occupational hygiene and environment protection.
Key Responsibilities:
- Ensure robust operations in alignment with quality, safety and environmental regulatory and site requirements.
- Co-ordinate with the relevant parties and contribute to the development of the monthly production schedule to enable timely material support to production, and to optimize the production.
- Assess situation, plan and implement all process campaign turnaround activities, as well as co-ordinate and track progress of shift teams to ensure production plan adherence.
- Identify and implement improvement to plant facilities, processes, methods of operations and turnaround, troubleshoot for process and equipment problems to minimize safety and quality risk as well as to ensure greater operational efficiency.
- Work on cutting time-wasters, extra costs, unnecessary effort as well as downtime causers.
- Lead or support quality or safety related investigation using appropriate problem-solving tool to determine the root causes and implement CAPA to prevent recurrence.
- Participate in the qualification works at OQ and PQ phases.
- Optimize process, production and maintenance systems focusing on improving OEE using GPS and lean tools.
Job Requirements
- B.S of Pharmacy or Engineering
- 1-3 years of experience in a Production, Quality and/or Engineering within the pharmaceutical industry.
- Good English & computer.
- In depth working knowledge of processing and packaging.
- In depth working knowledge of bottling and canning plant machinery and services.
- Ability to solve operational problems quickly.
- Good supervision and communication skills.
- Ability to train operators and provide them with right direction.
- Effective communicator
