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Sun Pharmaceutical Industries
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posted on 11 Oct 2021
I applied via Campus Placement and was interviewed before Oct 2020. There was 1 interview round.
I applied via Walk-in and was interviewed in Jul 2020. There was 1 interview round.
I applied via Other and was interviewed in Sep 2021. There was 1 interview round.
Pump seal arrangement and seal pressing setting work
Pump seals prevent leakage and maintain pressure
Seal arrangement involves selecting the right type of seal and installing it correctly
Seal pressing setting work involves adjusting the pressure on the seal to ensure proper functioning
Examples of pump seals include mechanical seals, lip seals, and labyrinth seals
posted on 1 Feb 2022
posted on 16 Aug 2024
I applied via Walk-in and was interviewed in Jul 2024. There was 1 interview round.
Company canteen bus is a shuttle service provided by the company to transport employees to and from the canteen during meal times.
Company canteen bus helps employees reach the canteen conveniently
It saves time for employees during meal breaks
Some companies offer free canteen bus service while others may charge a nominal fee
I applied via Naukri.com and was interviewed in Feb 2023. There were 2 interview rounds.
HPLC and GC detectors differ in their principles of detection and types of analytes they can detect.
HPLC detectors use UV-Vis, fluorescence, or electrochemical detection to analyze liquid samples.
GC detectors use thermal conductivity, flame ionization, or mass spectrometry to analyze gas samples.
HPLC is used for analyzing polar and non-volatile compounds, while GC is used for analyzing volatile compounds.
HPLC detectors...
I applied via Walk-in and was interviewed before Aug 2023. There was 1 interview round.
Process Validation is the documented evidence that a process consistently produces a product meeting its predetermined specifications and quality attributes.
Process Validation is a requirement in industries such as pharmaceuticals, medical devices, and food production.
It involves establishing documented evidence that a process is capable of consistently producing a product that meets its specifications.
Validation activ...
Exhibit batches are used for stability studies and regulatory submissions, while PPQ batches are used for process validation.
Exhibit batches are manufactured for stability studies and regulatory submissions.
PPQ (Process Performance Qualification) batches are manufactured for process validation.
Exhibit batches are typically larger in size compared to PPQ batches.
Exhibit batches are used to demonstrate the product's stab...
Parameters used in tablet manufacturing include formulation, compression force, tablet hardness, disintegration time, and friability.
Formulation - ingredients used in the tablet
Compression force - pressure applied during tablet compression
Tablet hardness - resistance to breaking
Disintegration time - time taken for tablet to break down in the body
Friability - tendency of tablet to break or crumble
LOD stands for Level of Detail. It refers to the amount of detail present in a model or visualization.
LOD is commonly used in computer graphics to optimize performance by displaying less detail when objects are far away.
It can also refer to the level of detail in data analysis, where different levels of granularity are used for different purposes.
For example, in a 3D video game, LOD may be used to switch between high-d...
Cleaning validation is the process of ensuring that a cleaning procedure effectively removes residues from equipment used in the manufacturing process.
Cleaning validation is essential in industries such as pharmaceuticals, food and beverage, and cosmetics.
It involves establishing documented evidence that the cleaning process consistently removes residues to predetermined levels.
Validation typically includes developing ...
Film coating is a process in which a thin layer of coating material is applied to a solid dosage form to improve appearance, taste, and stability.
Film coating helps protect the drug from moisture, light, and air
It can also mask the taste of the drug to improve patient compliance
Examples of film-coated tablets include Advil and Tylenol
Stratified sample analysis helps ensure representative sampling, while content uniformity test ensures consistency of active ingredients in a sample.
Stratified sample analysis involves dividing a population into subgroups based on certain characteristics before sampling.
Content uniformity test is used to ensure that the amount of active ingredient in each dosage unit is consistent.
Both techniques are important in quali...
CPP stands for Critical Process Parameters and CQA stands for Critical Quality Attributes of tablets.
CPP are the key variables that must be controlled to ensure the tablet manufacturing process is successful.
CQA are the characteristics that are critical to the quality of the tablet and must be monitored and controlled.
Examples of CPP include mixing time, compression force, and drying temperature.
Examples of CQA include...
Disintegration test is a test performed on tablets to determine the time it takes for a tablet to break down into smaller particles.
Disintegration test helps to ensure that the tablet will disintegrate properly in the body for effective drug release.
The criteria for disintegration test vary depending on the type of tablet and the intended use.
Common criteria include the time it takes for the tablet to disintegrate into...
Parameters used in dry granulation and reasons for its use.
Parameters include particle size, shape, and density of the powder material.
Reasons for dry granulation include avoiding use of solvents, improving flow properties, and enhancing compressibility.
Examples of dry granulation methods are slugging and roller compaction.
Some of the top questions asked at the Sun Pharmaceutical Industries Apprentice Trainee interview for experienced candidates -
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