Lupin
10+ TCS Interview Questions and Answers
Q1. What is corrective action and priventive action
Corrective action is taken to fix a problem that has already occurred, while preventive action is taken to avoid a problem from happening in the future.
Corrective action is reactive, while preventive action is proactive.
Corrective action is taken after a problem has been identified, while preventive action is taken before a problem occurs.
Examples of corrective action include repairing a machine that has broken down, while examples of preventive action include regular mainten...read more
Q2. Which type of pump and valve?
The type of pump and valve depends on the specific production process and requirements.
The selection of pump and valve depends on factors such as the fluid being handled, flow rate, pressure, temperature, and material compatibility.
Common types of pumps include centrifugal pumps, positive displacement pumps, and diaphragm pumps.
Common types of valves include ball valves, gate valves, globe valves, and butterfly valves.
For example, in a chemical production process, a centrifug...read more
Q3. What is distillation?
Distillation is a process of separating components of a liquid mixture based on their different boiling points.
Distillation involves heating a liquid mixture to vaporize the more volatile components.
The vapor is then cooled and condensed back into a liquid, resulting in the separation of the components.
The component with the lower boiling point will vaporize first and can be collected separately.
Common examples of distillation include the production of alcoholic beverages and...read more
Q4. Which type of distillation?
There are various types of distillation, such as fractional distillation, simple distillation, and vacuum distillation.
Fractional distillation is used to separate mixtures with close boiling points, such as in the separation of different components of crude oil.
Simple distillation is used to separate liquids with significantly different boiling points, such as in the purification of water.
Vacuum distillation is used to distill substances at lower temperatures by reducing the ...read more
Q5. What is change controls
Change controls are procedures used to manage changes to a product or process.
Change controls ensure that changes are properly evaluated, approved, and implemented
They help to prevent errors, defects, and deviations from specifications
Examples include changes to manufacturing processes, equipment, or materials
Documentation and record-keeping are important aspects of change controls
Q6. What is daviation
Deviation refers to the difference between an expected or planned outcome and the actual outcome.
It is a measure of how far a result is from the expected or average result.
Deviation can be positive or negative depending on whether the actual result is higher or lower than expected.
It is commonly used in statistics to measure the variability of a set of data.
For example, if the average height of a group of people is 5'6", but one person is 6'2", their height has a positive dev...read more
Q7. What is gmp And cgmp
GMP stands for Good Manufacturing Practice and cGMP stands for Current Good Manufacturing Practice.
GMP is a set of guidelines that ensure the quality and safety of pharmaceutical products.
cGMP is an updated version of GMP that is currently in use.
Both GMP and cGMP cover all aspects of the manufacturing process, including personnel, facilities, equipment, and documentation.
Adherence to GMP and cGMP is mandatory for pharmaceutical companies to obtain regulatory approval for the...read more
Q8. Types of change controls
Change controls are procedures used to manage changes to a product or process.
Document change requests
Evaluate impact of change
Obtain approval from relevant parties
Implement change
Verify effectiveness of change
Maintain records of change
Types include: design, process, equipment, material, and supplier changes
Q9. Types of daviation
There are various types of deviation that can occur in production processes.
Material deviation - when the raw materials used in production are different from the specified ones
Process deviation - when the production process deviates from the standard operating procedure
Equipment deviation - when the equipment used in production is not functioning as intended
Environmental deviation - when external factors such as temperature, humidity, or air quality affect the production proc...read more
Q10. Basic guidelines of gmp and unit operations
GMP stands for Good Manufacturing Practices, which are guidelines for ensuring the quality and safety of pharmaceutical products. Unit operations are individual steps in a manufacturing process.
GMP ensures that pharmaceutical products are consistently produced and controlled according to quality standards.
Unit operations are specific tasks or processes within a larger manufacturing operation, such as mixing, granulation, or drying.
GMP guidelines cover areas like personnel, pr...read more
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