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I applied via Referral and was interviewed before Apr 2022. There were 2 interview rounds.
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...
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...
I applied via Recruitment Consulltant and was interviewed before May 2021. There were 3 interview rounds.
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posted on 18 Aug 2023
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...
posted on 10 Feb 2025
I appeared for an interview in Jan 2025.
Seeking new challenges and growth opportunities
Desire for career advancement
Looking for new challenges
Seeking better work-life balance
Company restructuring or downsizing
Relocation to a new area
posted on 1 Aug 2024
I applied via Recruitment Consulltant and was interviewed before Aug 2023. There was 1 interview round.
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...
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
I applied via Campus Placement and was interviewed in Feb 2023. There were 3 interview rounds.
Logical questions and apparatus related questions and methods etc...
posted on 31 Mar 2022
I applied via Walk-in and was interviewed in Mar 2022. There were 3 interview rounds.
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.
posted on 21 Nov 2021
Critical process verification is the process of ensuring that critical processes are functioning as intended and meeting quality standards.
Identify critical processes
Define critical process parameters
Establish acceptance criteria
Verify critical process parameters
Document verification results
Implement corrective actions if necessary
posted on 7 Feb 2022
I applied via Naukri.com and was interviewed before Feb 2021. There were 2 interview rounds.
Somu Mounika
posted on 12 Sep 2024
I applied via Walk-in
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
Reasoning ,English,maths,gk.
based on 2 interviews
Interview experience
based on 25 reviews
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