Job responsibility Production officer liquid
Job Summary
To execute, and perform daily activities related to Oral Liquid section as per laid down procedures and systems. He is responsible for all below mentioned activities:
Job Responsibility
1. To check & maintain cleaning of m/c & area.
2. To check environmental condition (Temp.) of the area & report to Production Manager if any deviation observed.
3. Maintain status label in area, M/C and Equipments indicating activity.
4. To guide the helpers to practice good sanitation and health habits.
5. To check whether the helpers are properly dressed, as necessary to protect drug products from contamination.
6. To check whether the material pertaining to previous batch is removed, when ever required.
7. To take line clearance from QA before starting of process.
8. To check time & temperature during manufacturing process (syrup mfg., mixing of ingredients & filling etc.)
9. To check filled volume and seal integrity at the time of setting of machine and throughout the process of filling
as per schedule in the SOP.
10. To maintain all in process parameter checking and on line recording in BMR/BPR
11. To check proper labeling, appearance & printing during labeling process.
12. Drug product containers or closures shall be stored on pallet and suitably spaced to permit cleaning and inspection.
13. Cleaning, setting & Lubrication of machines.
14. Follow up of preventive maintenance schedule.
15. Daily balance verification and checking of monthly balance calibration status if not performed inform to QA/Production manager.
16. To keep & maintain issuance records of accessories & change parts of filling Machines.
17. To send and ensure sanitization of manufacturing and filling machine parts as per SOP.
18. To ensure that the product under packing has been inspected, weighed and checked before transfer to finished goods store.
19. Requisition of RM and PM for Batch and material issuance from ware house.
20. To report QA/production Manager if a deviation has occurred.
21. Send intimation to Q.A. to collect control sample, finished pack, stability and validation samples.
22. Reporting of day to day activity to Production Manager.
In the absence of candidate suitable person will be deputed to perform the above activities by HOD.
| Responsibility
Assigned by : _________________ (Sign) Name : Dated : _________________ |
Responsibility
Accepted by : ____________________ (Sign) Name :
Dated : ____________________
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process validation protocol for methylcobalamin niacinamide and pyridoxine injection
validation protocol of sterility test
sop for Analytical Method Transfer
Protocol for hold time study of sterile garments
sop for swab sampling for validation of clean surfaces
cleaning validation maco and noel calculation formula
sop for performance qualification for analyst
Sop for Validation report for disinfectant efficacy
Sop for Method validation report for bacterial endotoxin test
Sop for method validation microbiology sterility testing
sop for validation report for preservative efficacy test
sop for Protocol cum report for efficacy qualification of uv light
sop for validation protocol for uv light efficacy of dpb & laf
sop for cleaning validation protocol tablet manufacturing equipment
sop for cleaning validation protocol ointment manufacturing equipmentconcurrent process validation for rabeprazole ec and domperidone sr capsules
sop for Validation for cleaning procedure liquid injection
sop for Validation for cleaning procedure dry powder injection
Preparation Approval Control and Distribution of Master Formula Records
calibration policy for equipment and instruments
evaluation Sampling of Raw Materials questionnaire
training evaluation questionnaire
sop for approval of Contract Parties
sop for Operation and Cleaning of Purified Water Generation System
sop for Storage of Standard Weights
sop for Verification of Weighing Balance
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Sop for Submitting of Leave Application
sop for Accident Management Procedures
sop for Accident Management Procedures
Cleaning and colour coding of Factory Apparel (Clothes)
Job Responsibilities of Key Personnel
sop for Maintenance of Building
Destruction of Batch Production and Control Records BPCR
Procedure for Sampling of Rinse water Swab
Cleaning Validation of Equipment
Measurement and Recording of Temperature and Relative Humid
Sampling of Product at Intermediate Stages
Approval of Overprinting on Packing Material
sop for Procedure for Reprocessing
Preparation and Control of Master Batch Production and Control record
Issuance and Retrieval of Control documents
Calibration Policy for equipment
procedure for batch numbering system for products
sop for Handling of Incident during operation
Procedure for Allocation of Numbers for Machine Equipment
Validation and Qualification Facility System and Equipment
In-process Checks During Packing Operation
Operation and Calibration of Leak Test Apparatus
Operation and Calibration of Friability Tester
Access to Authorized Persons in Critical Areas
Operation Cleaning and Calibration of Digital Vernier Caliper
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Job Responsibility for Engineering