Job Responsibility Production
Job Summary
To plan, organize co-ordinate and control daily activities related to Production as per laid down
procedures and systems. He is responsible for all below mentioned activities:
Job Responsibility
The following shall be the principle duties and responsibilities of Production Manager deputed in the Plant.
1. To ensure that products are produced and stored according to the appropriate documentation in
order to maintain the product quality.
2. To approve the instructions relating to production operations and to ensure their strict implementation.
3. Weekly/Monthly production planning and to ensure the product availability as per the marketing
requirements & controlling the same as per the norms.
4. Generation of requisition of R.M. for batch preparation and its verification.
5. Manpower planning & allocation.
6. To ensure that the production records are evaluated and signed by an authorized person.
7. To ensure the qualification and maintenance of his department, premises and equipment.
8. To ensure that the required initial and continuing training of his department personnel is
carried out and adapted according to need.
9. The monitoring and control of the manufacturing environment.
10. To ensure maintenance of plant hygiene.
11. The designation and monitoring of storage conditions for materials and products.
12. The monitoring of compliance with the requirements of Good Manufacturing Practice.
13. Participation in management reviews of process performance, product quality and of the Pharmaceutical
Quality System and advocating continual improvement.
14. Ensuring that a timely and effective communication and escalation process exists to raise quality issues
to the appropriate levels of managements.
15. Preparation, review, controls and implementation of documents, wherever applicable.
16. Observation of all production area regarding process, area maintenance and qualification.
17. To review of all daily report received from various production officers/supervisor or chemist.
18. Indenting of spare parts required for machine maintenance/breakdown.
19. To prepare monthly W.I.P. record
20. To approve Master Formula, BMR and BPR records of drug products.
21. To take change control/deviation if required in production area.
22. To keep track for finished products until dispatched.
23. Trouble shooting on shop floor if problem observed.
24. Up keeping of machines.
25. Submission of report to Director.
- 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
Job Responsibility for Engineering
Job Responsibility for Quality Control
