Job Responsibility for Quality Control

Job Responsibility for Quality Control

 

Job Summary
To plan, organize, coordinate and control daily activities related to quality control as per laid down procedure

and systems. He is responsible for all below mentioned activities:
Job Responsibility
1. To ensure that all necessary testing is carried and the associated records evaluated.
2. To approve or reject raw materials, packing materials, intermediates, bulk and finished products.
3. To reviewed specifications, sampling instructions, test methods and other Quality Control procedures.
4. To ensure the qualification and maintenance of his/her department, premises and equipment.
5. To ensure that the appropriate validations are done.
6. To ensure that the required initial and continuing training to his department personnel is carried out and

adapted according to need.
7. The authorization of written procedures and other documents, including amendments.
8. To ensure maintenance of plant hygiene.
9. The approval and monitoring of suppliers of materials.
10. To ensure the retention of records.
11. The monitoring of compliance with the requirements of Good Manufacturing Practice.
12. The inspection, investigation and taking of samples, in order to monitor factors which may affect product quality.
13. Participation in management reviews of process performance, product quality and of the Pharmaceutical

Quality System and advocating continual improvement.
14. To ensure the required documentation like COA is completed in time of approving or rejecting

and RM/PM, sampling instructions.
15. To implement discipline, team work and good working atmosphere in the department.
16. To participate and contribution in achieving company objective as directed by the management.
17. To establish system, SOPs and documentation as per cGMP requirements.
18. To develop and check the artwork for new or existing products.
19. To release the finished product batch for sale / distribution.
20. To ensure the calibration work of laboratory instruments.
21. To develop methods for product testing.
22. To conduct audit and necessary documentation.
23. Responsible for overall responsibility of department.

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 process validation

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 equipment

concurrent 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

sop for validation plan

Preparation Approval Control and Distribution of Master Formula Records

calibration policy for equipment and instruments

sop for stability management

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

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 process validation

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 equipment

concurrent 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

sop for validation plan

Preparation Approval Control and Distribution of Master Formula Records

calibration policy for equipment and instruments

sop for stability management

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

sop for Receipt of Returned Goods from Market

Preparation of Master Formula Record MFR

  sop for Leave Policy

     Sop for Submitting of Leave Application

 sop for Accident Management Procedures

sop for Accident Management Procedures

Cleaning and colour coding of Factory Apparel (Clothes)

SOP for 5 S in pharma

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 Technology Transfer

sop for Handling of Incident during operation

Procedure for Allocation of Numbers for Machine Equipment

Validation and Qualification Facility System and Equipment

Allocation of Room Number

sop for Specimen Signatures

Preparation of SOP of SOP

In-process Checks During Packing Operation

Operation and Calibration of Leak Test Apparatus

Operation and Calibration of Friability Tester

sop for Scrap Management

Access to Authorized Persons in Critical Areas

Operation Cleaning and Calibration of Digital Vernier Caliper

sop for Sampling Procedure for Finished Product Samples

Job Responsibility for Engineering

Job Responsibility for Quality Control

 

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