Piramal Pharma Executive Interview Questions and Answers

Q1. Type of Granulation
Ans. 
Granulation can be either wet or dry, with each method having its own advantages and disadvantages.
• Granulation can be categorized as wet granulation or dry granulation.

• Wet granulation involves the addition of a liquid binder to the powder mixture, followed by drying and sizing.

• Dry granulation involves compacting the powder mixture without the use of liquid binders.

• Examples of wet granulation include high-shear granulat...read more
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Q2. What is automation
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Automation is the use of technology to perform tasks with minimal human intervention.
• Automation involves the use of machines, software, and other technologies to carry out tasks that would otherwise be done by humans.

• Examples of automation include robotic process automation (RPA), self-driving cars, and smart home devices.

• Automation can increase efficiency, reduce errors, and save time and money for businesses.
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Q3. Between the FBD FBP and FBE
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FBD FBP and FBE are different types of insurance policies.
• FBD (Full Business Day) insurance covers loss of income due to business interruption.

• FBP (Full Business Protection) insurance covers both property damage and business interruption.

• FBE (Full Business Enhancement) insurance offers additional coverage options to enhance a standard policy.
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Q4. Punch inspection and moc of dia and punch
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Q5. Gun validation gun nozzel size
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Q1. KF titrator calibrations
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Q1. Past experiences
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Q1. Name and address
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Q2. Previous company
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The aptitude test questions are fully depends on our knowledge related to chemistry.

Q1. They asks basic chemistry.
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Q2. Definitions like Normality, Molarity, Molality
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Normality, Molarity, and Molality are all measures of concentration used in chemistry.
• Normality measures the number of equivalents of a solute per liter of solution.

• Molarity measures the number of moles of a solute per liter of solution.

• Molality measures the number of moles of a solute per kilogram of solvent.

• Normality is used in acid-base reactions, while molarity and molality are used in a variety of chemical reactio...read more
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Q1. Tell me about Forced degradation study
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Forced degradation study is a process used to determine the stability of a drug substance or product under various stress conditions.
• Forced degradation studies involve subjecting the drug to conditions such as heat, light, humidity, and acid/base hydrolysis to simulate potential degradation pathways.

• The purpose of these studies is to identify degradation products, determine degradation pathways, and establish the stabi...read more
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Q2. Explain about Validation parameters
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Validation parameters are criteria used to ensure data input meets specified requirements.
• Validation parameters can include data type, length, format, range, and presence.

• For example, a validation parameter for a phone number field may require 10 digits and no special characters.

• Validation parameters help prevent errors and ensure data integrity.

• They are commonly used in form fields and database entries.
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Q3. Explain the problems faced in validations
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Validations in executive roles can face challenges due to lack of data accuracy, timeliness, and stakeholder alignment.
• Data accuracy issues can lead to incorrect decisions being made.

• Timeliness of data can impact the speed at which decisions can be made.

• Lack of stakeholder alignment can result in conflicting priorities and goals.

• Inconsistent validation processes across departments can lead to discrepancies in data inte
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Q4. Explain about validation plan
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A validation plan outlines the process for ensuring that a product or system meets specified requirements and standards.
• Defines the objectives and scope of validation activities

• Identifies the resources, responsibilities, and timelines for validation

• Specifies the methods and procedures for testing and evaluating the product or system

• Includes criteria for acceptance and rejection of validation results
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Q5. Calibration of HPLC
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Calibration of HPLC is a process of adjusting the settings of the High Performance Liquid Chromatography system to ensure accurate and reliable results.
• Calibration involves checking and adjusting the flow rate, detector sensitivity, and column efficiency.

• Regular calibration helps maintain the accuracy and precision of the HPLC system.

• Calibration standards are used to verify the performance of the system.

• Documentation o...read more
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