Akums Drugs & Pharmaceuticals Limited Senior Production Operator Interview Questions and Answers

Group members also strength and working important

Working fastly

Learning most important and fastly00q

Confidence and working together

Batch processing observed mostly important

Q1. Batch processing is technically and easily
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Q2. Batch processing is always smart work
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Q1. Entire hole company is dependent by hr
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Q2. All information provided the hr department
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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. Tell me about DCS HMI
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Q2. How to manage manpower &cost reduction
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Manpower can be managed by proper planning, training, and delegation. Cost reduction can be achieved through efficiency improvements, waste reduction, and negotiation with suppliers.
• Develop a detailed manpower plan based on workload and skill requirements

• Invest in training and development programs to upskill existing employees

• Delegate tasks effectively to ensure optimal use of manpower

• Implement efficiency improvements ...read more
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Q3. About documentation
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Q4. Production planning
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Q5. Batchprocess with safety
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Batch process with safety involves ensuring that production processes are carried out in a safe and controlled manner.
• Implementing safety protocols and procedures for each step of the batch process

• Regularly conducting safety audits and inspections to identify potential hazards

• Providing proper training to employees on safety measures and emergency procedures

• Using appropriate personal protective equipment (PPE) when hand...read more
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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
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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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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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