MSN Laboratories 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. 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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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. 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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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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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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Q1. How to check CAPA effectiveness?
Ans. 
CAPA effectiveness can be checked by reviewing the implementation of corrective and preventive actions, verifying if the root cause has been addressed, and monitoring for recurrence.
• Review the implementation of corrective and preventive actions taken in response to the CAPA.

• Verify if the root cause identified in the CAPA has been effectively addressed.

• Monitor the process or system to ensure that the issue does not recu...read more
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Q2. Elaborate Deviation work flow
Ans. 
Deviation work flow is a process that outlines how to handle and document any deviations from standard procedures or requirements.
• Deviation is identified and documented

• Root cause analysis is conducted to determine the reason for the deviation

• Corrective and preventive actions are proposed and implemented

• Impact assessment is done to evaluate the consequences of the deviation

• Approval process for the deviation and actions
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