job responsibility quality control micro
Job Summary:
To execute, and perform daily activities related to Quality Control department (Micro)
as per laid down procedures and systems. He is responsible for all below mentioned activities:
Job Responsibility
1. Supervise all Concern persons in his department.
2. Microbiological Analysis of raw material, water, finished product.
3. Maintain and control Area monitoring records in all departments.
4. Prepare media for daily microbial analysis and maintain their records.
5. Responsibility of receiving, reviving and sub culturing of microbial cultures and maintain the records.
6. Calibrates laboratory equipment, as instructed by Q.C. Head, in accordance with the established procedures.
7. Prepares report on test results and reports to Q.C. Head.
8. Checked & Record all daily activity in respective log book on daily basis.
9. Records use of Microbial Media &reagents on the stock register.
10. Preparation & review of SOP, STP, Finished Good Specification.
11. Responsible for releasing and rejecting finished products, starting and various activities according to the relevant SOPs.
12. Reports to Quality Head all the reagents, media, glassware and stationeries required.
13. Responsible for good cooperation among the laboratory personnel.
14. Responsible for the cleanliness and discipline in the working area.
15. Sampling of raw materials and water.
16. To plan the work distribution on daily basis.
17. Any other related duties as assigned by Quality Control Head.
18. Assists Quality Control Head in ensuring a high level of QC employee morale, a favorable
working environment and opportunities for employee department.
19. Makes progress reports on quality control issues, including stability reports
and in-process-control to Quality Control Head.
20. Keeps updated on GMP, Validation, Environmental monitoring and new analytical methods.
21. Any other related duties as assigned by Quality Control Head.
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
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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
sop for Sampling Procedure for Finished Product Samples