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I applied via Walk-in and was interviewed before Sep 2021. There were 2 interview rounds.
HPLC is a technique used in analytical chemistry to separate, identify, and quantify components in a mixture. Polar and nonpolar refer to the polarity of molecules.
HPLC stands for High-Performance Liquid Chromatography.
It is a widely used technique in pharmaceutical, chemical, and food industries.
HPLC separates components in a mixture based on their interactions with a stationary phase and a mobile phase.
The stationary...
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I applied via Recruitment Consulltant and was interviewed in Feb 2022. There were 2 interview rounds.
I applied via Walk-in and was interviewed in Dec 2022. There was 1 interview round.
I am interested in the company's commitment to quality and continuous improvement.
The company's strong focus on quality control and adherence to industry standards.
The company's track record of delivering high-quality products and services.
The company's dedication to continuous improvement and staying up-to-date with the latest advancements in quality control.
The company's emphasis on employee training and development ...
Oxidation is the loss of electrons and reduction is the gain of electrons.
Oxidation involves the loss of electrons from an atom or molecule.
Reduction involves the gain of electrons by an atom or molecule.
Oxidation and reduction always occur together in a chemical reaction.
Examples include rusting of iron (oxidation) and photosynthesis (reduction).
pH is a measure of acidity or alkalinity of a solution. It ranges from 0 to 14, with 7 being neutral.
pH stands for 'potential of hydrogen'
It is measured on a scale of 0 to 14
A pH of 7 is neutral, below 7 is acidic, and above 7 is alkaline
pH can be measured using pH paper, pH meter, or indicators like litmus paper
Examples of pH values: lemon juice (pH 2), water (pH 7), baking soda (pH 9)
I appeared for an interview in May 2017.
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 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...
posted on 25 Feb 2024
I applied via Referral and was interviewed before Feb 2023. There were 2 interview rounds.
CPP parameters refer to Critical Process Parameters which have a significant impact on Critical Quality Attributes (CQA) in manufacturing processes.
CPP parameters are specific process variables that must be controlled within a certain range to ensure product quality.
Examples of CPP parameters include temperature, pressure, flow rate, and mixing speed.
The impact of CPP parameters on CQA can be seen in the final product ...
The annual report submission procedure for USFDA approved products involves compiling data on product performance, safety, and compliance with regulations.
Compile data on product performance, safety, and compliance with USFDA regulations
Submit the annual report to the USFDA within the specified deadline
Include information on any changes in manufacturing processes or product labeling
Ensure all data submitted is accurate
Executive
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Chemist
432
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Junior Executive
410
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310
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