Macleods Pharmaceuticals Junior Production Officer Interview Questions and Answers

Q1. General questions about your company
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Q1. What are you doing in previous company? Safety, GMP, technical,
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Q1. Which university you have study
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Q1. 1) What is Distillation column 2) Chlorine Gas TLV limit 3) All Reactor Types and handling
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Questions related to distillation column, chlorine gas TLV limit, and reactor types and handling.
• Distillation column is a separation process used to purify or separate components of a mixture.

• TLV limit for chlorine gas is 1 ppm (parts per million).

• Reactor types include batch, continuous stirred tank, plug flow, and fluidized bed reactors. Handling involves proper safety measures and monitoring of reaction conditions.
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Q1. 1) Sallary Discussion
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Q1. What is tablets define
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Q2. Which types of capsule
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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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Q1. Experienced in Pharmaceutics
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Q2. Troubleshooting
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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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