Key Responsibilities:
- Assist the Production Manager to plan the production schedule.
- Monitor day-to-day operation to ensure the operation is smooth and meets the production schedule.
- Ensure that the entire operations are following EHS, Good Manufacturing Practices (GMP), and Standard Operation Procedure (SOP) requirements with good quality culture.
- Ensure the documentation record and plant 3S is properly maintained.
- Review production process and documents daily (Batch record, log sheet, check sheet, etc.).
- Feedback, investigate and submit reports on operation abnormality, incidents, etc.
- Training, coaching, and motivating staff to meet the present and future needs of the manufacturing operations, cultivating a good quality culture mindset within the department.
- To take charge of Work In Progress (WIP) check weekly and monthly, provide WIP & Production report.
- Assist Production Manager to liaise with suppliers or contractor.
- Contribute ideas for continuous improvement (Work procedure, Cost deduction, Automation, EHS, etc.).
- To perform other tasks in the manufacturing division as and when required.
- To work independently with minimum supervision, be resourceful and self-motivated.
- Take charge of departmental employee attendance checking and submission.
Requirements:
- Minimally Bachelor's Degree in Chemistry, Chemical Engineering or any relevant fields.
- At least 2 years of relevant working experience in an API pharma supervisory role.
- Independent and fast learner with a positive attitude.
- Process automation and IT knowledge will be an advantage.
