Intas Pharmaceuticals Executive Quality Assurance Interview Questions and Answers

Q1. Its It's about discuss whole works experience
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Q1. Its about work profile
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Q1. As usual about money
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Q1. All IPQA activities with cGMP Norms
Ans. 
IPQA activities refer to In-Process Quality Assurance activities that ensure compliance with cGMP norms.
• IPQA activities involve monitoring and inspecting the manufacturing process to ensure quality standards are met

• Examples of IPQA activities include in-process checks, sampling, and documentation review

• IPQA activities are essential for maintaining product quality and compliance with cGMP norms
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Q2. Data integrity,and QMS.
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Reasoning ,English,maths,gk.

Q1. Stability ,salary
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Q1. Why are you looking for a change?
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Q2. What are your salary expectations?
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Q3. What is your family background?
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Q4. Share details of your previous job.
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Q5. Tell me about yourself.
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Q6. Why you are relocating?
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Q7. How experience you have?
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Q8. Current how much CTC you have?
Ans. 
My current CTC is confidential.
• I prefer not to disclose my current CTC as it is confidential.

• I am open to discussing my salary expectations for this role.

• I believe my skills and experience make me a strong candidate for this position.

• I am willing to negotiate a fair and competitive salary based on the responsibilities and requirements of the role.
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Q1. Tell me about your self
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Q1. What is APQR What is validation
Ans. 
APQR stands for Annual Product Quality Review. Validation is the process of establishing documented evidence that provides a high degree of assurance that a specific process will consistently produce a product meeting its predetermined specifications and quality attributes.
• APQR is a review conducted annually to evaluate the quality standards of a product throughout its lifecycle.

• Validation involves documenting evidence...read more
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Q1. What is your current CTC
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Logical questions and apparatus related questions and methods etc...

Q1. Communication skills Critical thinking questions
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Q1. 1) How to fix impurities limit? २) What are the amv parameters?
Ans. 
Fixing impurities limit involves identifying the source of impurities and implementing measures to reduce or eliminate them.
• Conduct a risk assessment to identify potential sources of impurities

• Establish impurity limits based on regulatory requirements and product specifications

• Implement measures to reduce or eliminate impurities, such as process optimization or equipment upgrades

• Monitor impurity levels regularly to ens...read more
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Q2. What are the amv parameters?
Ans. 
AMV parameters are used in video encoding to optimize the quality and compression of the video.
• AMV stands for Anime Music Video, a popular video format for fan-made music videos.

• AMV parameters include frame rate, bit rate, resolution, and codec.

• Optimizing these parameters can improve video quality and reduce file size.

• For example, lowering the bit rate can reduce file size but may result in lower video quality.

• Choosing...read more
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I love industry job.there is a lot of interest in quality assurance in the industry as well.

Q1. Name, place, qualification and hobbies
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Q2. What is tablet evaluation parameters
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Q3. What is emulsion and suspension
Ans. 
Emulsion is a mixture of two immiscible liquids, while suspension is a mixture of solid particles in a liquid.
• Emulsion is a mixture of two immiscible liquids, where one liquid is dispersed in the other.

• Examples of emulsions include milk, mayonnaise, and vinaigrette.

• Suspension is a mixture of solid particles in a liquid, where the particles are not dissolved.

• Examples of suspensions include muddy water, blood, and paint.

• ...read more
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Q4. What is capsule and tablets
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Q5. What is friavility test
Ans. 
A friability test is a method to determine the durability of tablets or granules by measuring their tendency to break or crumble.
• It is a quality control test performed on tablets or granules

• The tablets or granules are subjected to mechanical stress by tumbling them in a rotating drum

• The percentage weight loss due to breakage or crumbling is measured and compared to the acceptable limit

• It helps to ensure the tablets or ...read more
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