Pfizer Production Officer Interview Questions and Answers

Q1. What is your project
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Q2. What is molarity
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Q1. What is the disintegration time of uncoated table
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Q2. What is the role of vent filter in rmg
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Vent filter in RMG plays a crucial role in preventing contamination and maintaining the required air flow.
• Vent filter helps in maintaining the required air flow in the RMG machine.

• It prevents contamination by filtering out dust, particles, and other impurities from entering the machine.

• Regular maintenance and replacement of vent filters are necessary to ensure optimal performance.

• Vent filter also helps in maintaining t...read more
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Sir please find opportunity skills and well working properly and good behaviour all

Training on my self profamnce cGmp and GDP growth and development projects worth in understanding in training period of the following cGmp documents mantine for job opportunities

Q1. What is tablet ?
Ans. 
A tablet is a small, portable computer that typically has a touchscreen for input and display.
• Portable device with touchscreen display

• Used for various purposes like browsing, gaming, and productivity

• Common operating systems include iOS and Android

• Examples: iPad, Samsung Galaxy Tab, Microsoft Surface
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Q2. Defect of tablet
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Defect of tablet can be due to issues in formulation, manufacturing process, or packaging.
• Possible defects include chipping, cracking, discoloration, or improper dissolution.

• Causes can range from incorrect ingredient ratios to inadequate compression during manufacturing.

• Quality control measures such as visual inspection, hardness testing, and dissolution testing can help identify defects.

• Proper storage conditions and p...read more
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Q3. What is Disintegration ot tablet
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Q4. What is tablet DT test for not dissolved
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Tablet DT test is a test to determine the dissolution time of a tablet in a specific medium.
• Tablet DT test is conducted to assess the time it takes for a tablet to dissolve completely in a specified medium.

• It helps in evaluating the effectiveness of the tablet's formulation and its ability to release the active ingredient.

• The test involves placing the tablet in a dissolution apparatus with a specific medium and monitor...read more
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Q5. What is pharmaceutical plant in method
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Physical methods
Radiation method
Tharmal method
Filtration method
Chemical method
Gasses method
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Q1. Personal details family background
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Q1. Background of work, flexibiltiy
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Q2. Experience, equipment exposure
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Q1. Handling of Validation
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Validation in production involves ensuring that processes and products meet quality standards.
• Validation involves verifying that equipment, processes, and systems are operating correctly and consistently.

• Validation also includes confirming that products meet specifications and quality standards.

• Documentation of validation activities is essential for regulatory compliance and continuous improvement.

• Examples of validatio...read more
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Q2. Operations of reactors, centrifuge, sparker filters, anfds, ejectors.
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Q3. Handling of Qualifications
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Q4. Handling of Safety permits
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Safety permits are essential for ensuring compliance with regulations and maintaining a safe work environment.
• Safety permits are required for certain activities or equipment to ensure they meet safety standards.

• Production officers must be familiar with the types of safety permits needed in their industry.

• They are responsible for obtaining and renewing safety permits as needed.

• Failure to comply with safety permit requir...read more
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Q5. Operation of Distillation
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Distillation is a process used to separate components of a liquid mixture based on differences in boiling points.
• Distillation involves heating the liquid mixture to create vapor, then cooling the vapor to condense it back into liquid form.

• The components with lower boiling points will vaporize first and be collected as the distillate, while the components with higher boiling points remain in the original container.

• Commo...read more
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Q6. Handling of Deviations
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Deviations in production processes must be promptly identified, investigated, and documented to ensure product quality and compliance.
• Deviation should be reported immediately to the appropriate personnel

• Investigate the root cause of the deviation

• Document all findings and actions taken

• Implement corrective and preventive actions to prevent recurrence

• Review and approve deviation reports before closure
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Q1. Handling of CAPA
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CAPA refers to Corrective and Preventive Actions taken to address non-conformities and prevent recurrence.
• Identify the root cause of the issue

• Develop a corrective action plan to address the issue

• Implement the corrective action plan

• Monitor the effectiveness of the corrective action

• Implement preventive actions to prevent recurrence
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Q2. What is DATA INTIGRIY
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Data integrity refers to the accuracy, consistency, and reliability of data throughout its lifecycle.
• Ensuring data is accurate and reliable

• Maintaining consistency of data

• Preventing unauthorized access or modifications

• Implementing data validation processes

• Regularly backing up data to prevent loss
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Q3. Handling Solvents
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Q4. Handling of Batch failures
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Batch failures should be analyzed to identify root causes and prevent future occurrences.
• Investigate the root cause of the batch failure

• Implement corrective actions to prevent future failures

• Document the findings and actions taken for future reference

• Communicate with relevant stakeholders about the batch failure and resolution

• Conduct a review of the production process to identify potential areas for improvement
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Q5. Handling of Deviations
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Handling of deviations involves identifying, investigating, and resolving any deviations from standard procedures or specifications.
• Deviation should be documented and reported immediately

• Investigate root cause of deviation

• Implement corrective and preventive actions

• Review and update procedures to prevent future deviations
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Q1. Current Role and responsibilities
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Q2. Personal information
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Q3. Salary discussion
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Basics of chemistry and industrial safety

Current affairs and current issues in industrial job

Q1. What is chlorination
Ans. 
Chlorination is the process of adding chlorine to water or other substances to disinfect and kill bacteria and other harmful microorganisms.
• Chlorination is commonly used in water treatment plants to make drinking water safe for consumption.

• It is also used in swimming pools to kill bacteria and prevent the spread of waterborne illnesses.

• Chlorination can be done using chlorine gas, liquid chlorine, or chlorine compounds ...read more
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Q2. What is unit operation and process
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Unit operation is a single step in a process while process is a series of interconnected unit operations.
• Unit operation is a distinct step in a chemical engineering process.

• Process is a series of interconnected unit operations that work together to achieve a desired outcome.

• Examples of unit operations include distillation, filtration, and mixing.

• Examples of processes include production of pharmaceuticals, food processi
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