Sun Pharmaceutical Industries Production Support Executive Interview Questions and Answers

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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Q1. Area qualifications
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Q2. Equipment validation
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Q1. Manufacturing process
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Q2. Trouble shooting
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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
Ans. 
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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Handling of trouble shooting, block maintain capabilities, processes related documents, and forms which are handled in manufacturing

Q1. Process related impurities,
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Q2. Safety precautions at manufacturing
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Safety precautions at manufacturing include proper training, use of personal protective equipment, regular equipment maintenance, and emergency response plans.
• Provide comprehensive safety training to all employees

• Ensure proper use of personal protective equipment (PPE)

• Regularly inspect and maintain equipment to prevent accidents

• Develop and implement emergency response plans for various scenarios
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Q3. Achievement at career
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Q1. What is meadia fill ?
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Q2. What is SCDM ?
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Q1. Mfg Machine opereating
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Q2. Production .mfg
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Q3. Filling machine
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Q4. Tablet Cotting department
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Q5. Granulation department
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Q1. What is your project
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Q2. What is molarity
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Q1. What is chemistry
Ans. 
Chemistry is the study of matter, its properties, composition, and interactions.
• Chemistry involves understanding the structure and behavior of atoms and molecules

• It explores how substances react with each other to form new substances

• Chemistry is used in various industries such as pharmaceuticals, agriculture, and manufacturing
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Q2. How many batch change in reactor
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The number of batch changes in a reactor can vary depending on the production schedule and process requirements.
• The number of batch changes in a reactor is typically determined by the production plan and the capacity of the reactor.

• Factors such as reaction time, temperature, pressure, and product yield can also influence the frequency of batch changes.

• For example, a reactor used for continuous production may have fewer...read more
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Q3. How many classes in safety
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There are several classes in safety, including general safety, chemical safety, fire safety, electrical safety, and more.
• General safety covers basic safety practices and procedures for all employees.

• Chemical safety focuses on handling, storing, and disposing of hazardous chemicals.

• Fire safety includes fire prevention, evacuation procedures, and proper use of fire extinguishers.

• Electrical safety involves safe practices ...read more
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Q4. What is API in pharmacy
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Q5. ALCOA FULL meaning
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ALCOA stands for Attributable, Legible, Contemporaneous, Original, and Accurate in the context of data integrity.
• Attributable - Data should be traceable to its source.

• Legible - Data should be clear and easy to read.

• Contemporaneous - Data should be recorded at the time of observation.

• Original - Data should be the first recording of the information.

• Accurate - Data should be error-free and true to the actual observation.
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