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Microbial limit test is a method used to determine the total number of viable microorganisms present in a sample.
It is performed to ensure the quality and safety of pharmaceuticals, cosmetics, food products, and other substances.
The test involves inoculating the sample onto specific growth media and incubating it under suitable conditions.
After incubation, the colonies formed are counted and compared to established lim...
Microbial testing of water involves analyzing water samples for the presence of microorganisms to ensure water safety.
Collect water samples from different sources for testing
Use various methods such as culture-based techniques, molecular techniques, and rapid testing kits
Identify and quantify bacteria, viruses, and parasites in the water
Interpret test results to determine if water is safe for consumption
Common tests in...
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I applied via Approached by Company and was interviewed before Jun 2021. There were 2 interview rounds.
I appeared for an interview in Nov 2020.
P2P cycle refers to the process of procuring goods or services from a supplier and making payments for them.
The cycle starts with identifying the need for goods or services.
The next step is to create a purchase order (PO) and send it to the supplier.
The supplier then delivers the goods or services and sends an invoice to the buyer.
The buyer verifies the invoice and matches it with the PO and goods received.
If everythin...
I applied via Campus Placement and was interviewed before May 2020. There were 3 interview rounds.
posted on 19 Dec 2019
I applied via Referral and was interviewed before Dec 2018. There were 3 interview rounds.
The Ich limit for methanol is 0.6% and it is classified as a class 3 solvent.
The Ich limit for methanol refers to the maximum allowable amount of methanol in a pharmaceutical product.
The Ich limit for methanol is set at 0.6%, meaning that the concentration of methanol should not exceed 0.6% in the product.
Methanol is classified as a class 3 solvent according to the International Council for Harmonisation of Technical R...
The specification limit for known and unknown impurities varies depending on the specific substance being tested.
The specification limit for known impurities is typically set by regulatory agencies or pharmacopoeias.
For example, the United States Pharmacopeia (USP) sets limits for known impurities in pharmaceutical substances.
The specification limit for unknown impurities is usually determined through method validation...
I applied via Referral and was interviewed before Jun 2021. There were 2 interview rounds.
I appeared for an interview in Mar 2021.
I applied via Walk-in and was interviewed in Oct 2020. There were 3 interview rounds.
CAPA stands for Corrective and Preventive Action, while OOS stands for Out of Specification.
CAPA is a process used to identify, investigate, and resolve quality issues.
OOS refers to a result that falls outside of predetermined specifications.
CAPA and OOS are both important in maintaining quality control in various industries.
In the medical field, CAPA and OOS are crucial for ensuring patient safety and regulatory compl
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