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| Job Location | Gandhidham |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | harma / Biotech |
| Functional Area | Production |
| EmploymentType | Full-time |
Maintains c-GMP practices along with documentation in various records.Checks In process parameters and maintain its documentations including finished goods checking.Fills batch manufacturing/packing record correctly before submission to his superiors.Imparts on job/ Classroom training to the workmen for SOP and cGMP systems.Participates in Validation activities as per the protocol.Raises the material requisition note (MRQN) wherever extra quantity of packing material is required.Prepares the material return note (MRN) after the batch/product campaign.Prepares the line rejection note (LRN) wherever required.Verifies the balances on daily and monthly basis.Helps in investigation of market complaints.Maintain the document as per Requirement of ISO 9001 and ISO 13485.Knowledge and involvement in Operational Excellence activities.Checks all the calibration tags of equipment, instruments and fire extinguisher for their due date time to time.
Keyskills :
productionqmsschedulingmanufacturingroductionchemistproductionofficerplanningasepticprocessointmentnon-sterileophthalmictechniquesisoaudit