Sudeep Pharma QA Executive Interview Questions and Answers

Q1. What is ph and explain about ph
Ans. 
pH is a measure of acidity or alkalinity of a solution on a scale of 0 to 14.
• pH stands for 'potential of Hydrogen'

• pH scale ranges from 0 (most acidic) to 14 (most alkaline)

• Neutral pH is 7, like pure water

• Acids have pH below 7, bases have pH above 7

• pH is important in various industries like agriculture, food, and medicine
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Q1. Difference Between Validation & Calibration
Ans. 
Validation ensures a process or system meets requirements, while calibration ensures accuracy of measurements.
• Validation confirms that a process or system meets predetermined specifications and requirements.

• Calibration involves comparing measurements of an instrument or device to a known standard to ensure accuracy.

• Validation is more about ensuring the right process is being used, while calibration is about ensuring ac...read more
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Q2. How Is Forced Degradation Study Performed
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Q1. Basic questions related to production ...chemistry....abbreviations etc
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Q2. Definition of QA/QC? Chemical formula of plaster of paris?
Ans. 
QA/QC stands for Quality Assurance/Quality Control. Plaster of Paris chemical formula is CaSO4.1/2H2O.
• QA/QC is a set of activities that ensure quality in a product or service.

• QA focuses on preventing defects while QC focuses on identifying and correcting defects.

• Plaster of Paris is a white powder made from gypsum that hardens when mixed with water.

• Its chemical formula is CaSO4.1/2H2O, which means it contains one molecu...read more
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Q1. About inroduction.....project details etc.
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Q1. Questions related to pursued degree.....details in depth....etc
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Test related of my subject knowledge

Q1. Quality head ask questions about pharmacy act and schedules in pharmacy.
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Q1. General introduction
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Q1. What are the contents process validation protocol & report
Ans. 
The contents of a process validation protocol and report include detailed information about the validation process and its results.
• Purpose and scope of the validation

• Description of the process being validated

• Validation criteria and acceptance criteria

• Methods and procedures used for validation

• Sampling plan and sample size

• Data collection and analysis

• Results and conclusions

• Recommendations for process improvements

• Signature
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Q1. About company, experience and salary. What is the purpose of job change?
Ans. API, 8 years , company standard, for carrier growth and learning
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Q1. What is gmp in pharma
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Q2. What is ALCOA principle
Ans. 
ALCOA principle is a guideline for ensuring data integrity in regulated industries, emphasizing data should be attributable, legible, contemporaneous, original, and accurate.
• Attributable - Data should be traceable to its source.

• Legible - Data should be clear and easy to read.

• Contemporaneous - Data should be recorded at the time of observation.

• Original - Data should be the first recording of the information.

• Accurate - D...read more
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Q1. Those who work there have so much job experience
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Q2. They are expecting so much salary
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