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I applied via Company Website and was interviewed before Dec 2018. There were 3 interview rounds.
There are several types of validations used in manufacturing processes.
Process validation: ensuring that a manufacturing process consistently produces a product that meets predetermined quality standards.
Equipment validation: verifying that manufacturing equipment is properly calibrated and functioning correctly.
Cleaning validation: confirming that cleaning procedures effectively remove residues and contaminants from e...
Process validations are used to ensure that manufacturing processes consistently produce products of the desired quality.
There are three types of process validations: prospective, concurrent, and retrospective.
Prospective validation is performed before a new process is put into production.
Concurrent validation is performed during regular production to ensure ongoing process control.
Retrospective validation is performed...
Activities in QMS include establishing quality objectives, conducting audits, managing nonconformities, and continuous improvement.
Establishing quality objectives to ensure products meet customer requirements
Conducting audits to assess compliance with quality standards
Managing nonconformities by identifying and addressing deviations from quality requirements
Implementing corrective and preventive actions to prevent recu...
Parameters in an analytical method validation include accuracy, precision, specificity, linearity, range, and robustness.
Accuracy: the closeness of test results to the true value
Precision: the closeness of agreement between individual test results
Specificity: the ability to assess the analyte in the presence of other components
Linearity: the ability to obtain test results that are directly proportional to the analyte c...
Forced degradation studies are conducted to determine the stability and degradation pathways of a drug or product.
Forced degradation studies are performed to simulate the degradation of a drug or product under extreme conditions.
The purpose is to understand the degradation pathways, identify potential impurities, and evaluate the stability of the drug or product.
These studies help in establishing appropriate storage co...
Further action should be taken to prevent or mitigate degradation in manufacturing processes.
Identify the root cause of degradation
Implement corrective actions to address the root cause
Monitor and measure the effectiveness of the corrective actions
Continuously improve processes to prevent future degradation
Train and educate employees on best practices and quality standards
Implement preventive maintenance programs
Regula...
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I applied via Referral and was interviewed before May 2021. There were 3 interview rounds.
I applied via Referral and was interviewed before May 2021. There were 3 interview rounds.
I applied via Walk-in and was interviewed in Nov 2020. There were 5 interview rounds.
I was interviewed in Mar 2021.
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I applied via Walk-in and was interviewed before Apr 2022. There was 1 interview round.
I applied via Approached by Company and was interviewed before Sep 2023. There were 2 interview rounds.
posted on 7 May 2023
I applied via Naukri.com and was interviewed before May 2022. There were 2 interview rounds.
posted on 18 May 2024
Production Supervisor
40
salaries
| ₹0 L/yr - ₹0 L/yr |
QC Chemist
32
salaries
| ₹0 L/yr - ₹0 L/yr |
Assistant Manager
27
salaries
| ₹0 L/yr - ₹0 L/yr |
Executive
18
salaries
| ₹0 L/yr - ₹0 L/yr |
Shift Incharge
15
salaries
| ₹0 L/yr - ₹0 L/yr |
Aarti Industries
Vinati Organics
Atul
Solvay Specialities