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Cipla
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I applied via Walk-in and was interviewed in Sep 2023. There was 1 interview round.
Granulation process involves the formation of granules from powder particles.
Powder particles are agglomerated to form granules.
Granulation can be achieved through wet or dry methods.
Wet granulation involves adding a liquid binder to the powder mixture.
Dry granulation involves compacting the powder mixture without the use of liquids.
Examples of granulation equipment include fluid bed granulators and roller compactors.
Capsules are solid dosage forms in which the drug is enclosed in a hard or soft soluble container.
Capsules can be classified as hard gelatin capsules or soft gelatin capsules.
Hard gelatin capsules are made of two pieces that fit together, while soft gelatin capsules are made of a single piece.
Capsules can be filled with powder, granules, pellets, or liquids.
Examples of capsules include Tylenol capsules and Vitamin E ca
Two types of row material are natural materials and synthetic materials.
Natural materials come from plants, animals, or minerals (e.g. cotton, wool, wood)
Synthetic materials are man-made through chemical processes (e.g. plastic, nylon, polyester)
Raw material dispensing science involves the accurate measurement and distribution of materials for production.
Raw material dispensing involves measuring and distributing materials needed for production processes.
Accurate measurements are crucial to ensure the quality and consistency of the final product.
Proper labeling and storage of raw materials is essential to prevent mix-ups and contamination.
Automated dispensing ...
I applied via Walk-in and was interviewed before Dec 2022. There were 2 interview rounds.
I applied via Company Website
Cipla interview questions for designations
I applied via Naukri.com and was interviewed in Apr 2022. There was 1 interview round.
I applied via Walk-in and was interviewed before Apr 2022. There was 1 interview round.
I applied via Referral and was interviewed in Nov 2020. There was 1 interview round.
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...
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...
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...
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
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
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
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
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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Senior Executive
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Assistant Manager
2.7k
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Deputy Manager
1.1k
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Executive
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Area Business Manager
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| ₹4.3 L/yr - ₹12 L/yr |
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