The job duties for this position include but are not limited to the following:
- Organize and oversee the activities related to the manufacturing of tablets and capsules to include delivery, in-process samples in a defined schedule.
- Review and compile the documents generated during the production of tablets and capsules such as Batch Manufacturing Record (BMR), PQ protocol.
- Perform SAP entry during and finish batches product.
- Make equipment part list required for machine, and support supervisor to order it
- Assign work to operators according to product schedule.
- Make sure to transfer request of product material batches from warehouse to
- Manufacturing and vice versa.
- Update attendance.
- Ensure and compliance with safety, quality, productivity, and performance expectations and execution of manufacturing operations.
- Review batch record after finishing each step for correctness.
- Provide support to the operators in regarding day-to-day production activities such as trouble shooting and other work tasks.
- Make sure correct ness of product log in and yield of product with BMR Correctness
- online.
- Schedule cleaning validation with request as required for equipment.
- Work with Integrated Product Development (IPD)/R&D on the execution of bio-batches (abbreviated new drug applications - ANDA) and validation batches.
- Support supervisor as needed to day to day activity to achieve productivity and compliance.
- Coordinate to implementation of current good manufacturing practices (cGMP) and safety practices in the operations and manufacturing of products.
- Ensure to maintain cleanliness working environment.
- Work closely with Manufacturing Supervisor for Driving operational excellence and flawless execution in order to achieve site quality and manufacturing objectives.
Job Type: Full-time
Salary: $21.00 per hour
Work Location: On the road
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