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I applied via Walk-in and was interviewed before Sep 2022. There were 2 interview rounds.
I was interviewed in Oct 2020.
Equipment Qualification is the process of ensuring that equipment is suitable for its intended use.
Equipment Qualification involves testing and verifying that equipment meets certain standards and specifications.
It includes installation qualification, operational qualification, and performance qualification.
Examples of equipment that may require qualification include laboratory instruments, manufacturing equipment, and...
Validation is the process of ensuring that a product or service meets the requirements and specifications of the customer.
There are two types of validation: process validation and product validation.
Process validation involves validating the manufacturing process itself, while product validation involves validating the final product.
The content in process validation includes process design, process qualification, and c...
The range of differential pressure in Powder processing area varies depending on the clean room classification.
The differential pressure in a clean room for powder processing should be positive to prevent contamination from entering the room.
The range of differential pressure for a clean room in PP area can be between 10-60 Pascals depending on the classification.
The clean room classification for PP area can range from...
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I applied via Walk-in and was interviewed in Mar 2021. There were 3 interview rounds.
Density is the measure of mass per unit volume of a substance.
Density is calculated by dividing the mass of a substance by its volume.
It is a physical property that can be used to identify substances.
The density of a substance can change with temperature and pressure.
Water has a density of 1 gram per cubic centimeter.
The density of air is much lower than the density of water.
I applied via Referral and was interviewed before Dec 2019. There was 1 interview round.
I applied via Walk-in and was interviewed before Aug 2023. There was 1 interview round.
Good Manufacturing Practices (GMP) are guidelines and regulations set by regulatory agencies to ensure the quality and safety of products during manufacturing.
GMP are a set of guidelines and regulations that ensure products are consistently produced and controlled according to quality standards.
They cover all aspects of production, from the materials used to the facilities and equipment.
Examples of GMP include proper d...
ALCOA++ is a set of principles used in data integrity to ensure data is Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available.
Attributable - Data should be traceable to its source.
Legible - Data should be clear and easy to read.
Contemporaneous - Data should be recorded at the time of observation.
Original - Data should be the first recorded and not a copy.
Accurate - Da...
I applied via Recruitment Consultant and was interviewed before Jun 2020. There were 4 interview rounds.
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Officer
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Production Officer
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Biocon Limited
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