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HPLC and GC are analytical techniques used to separate, identify, and quantify components in a mixture.
HPLC (High Performance Liquid Chromatography) is used for separating compounds in a liquid mixture based on their interaction with a stationary phase and a mobile phase.
GC (Gas Chromatography) is used for separating compounds in a gas mixture based on their partitioning between a stationary phase and a mobile phase.
Bo...
HPLC is used to determine the presence and quantity of various substances in a sample.
HPLC stands for High Performance Liquid Chromatography.
It is commonly used in pharmaceutical, environmental, and food industries.
HPLC separates and analyzes compounds in a sample based on their interactions with a stationary phase and a mobile phase.
It is a powerful tool for identifying and quantifying components in complex mixtures.
E...
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I applied via Walk-in and was interviewed in May 2022. There were 2 interview rounds.
I applied via Referral and was interviewed in Aug 2021. There were 3 interview rounds.
I applied via Walk-in and was interviewed in Dec 2021. There were 4 interview rounds.
posted on 24 Aug 2024
I applied via Walk-in and was interviewed in Jul 2024. There were 2 interview rounds.
About academic basic multiple choice questions
posted on 9 Oct 2023
I applied via Naukri.com and was interviewed before Oct 2022. There were 2 interview rounds.
I applied via Walk-in and was interviewed in Mar 2021. There were 3 interview rounds.
I applied via Approached by Company and was interviewed before Sep 2021. There were 2 interview rounds.
posted on 11 Feb 2024
I applied via Approached by Company and was interviewed in Aug 2023. There were 3 interview rounds.
Change control is a process used to manage and document changes to a system or process.
Change control ensures that changes are properly reviewed, approved, and implemented.
It helps to minimize risks and ensure that changes do not negatively impact the quality or functionality of the system.
Change control typically involves documenting the change request, assessing its impact, obtaining necessary approvals, implementing...
Process validation is the process of establishing documented evidence that a process consistently produces a product meeting predetermined specifications.
There are three types of process validation: prospective validation, concurrent validation, and retrospective validation.
Prospective validation is conducted before the process is put into routine use.
Concurrent validation is performed during routine production.
Retrosp...
Audit trail is maintained by documenting and tracking all activities and changes made to a system or process.
Audit trail is created by recording all actions, events, and transactions that occur within a system.
It helps in ensuring accountability, traceability, and compliance with regulations.
Audit trail can be established through the use of logs, timestamps, and version control.
It is important to capture relevant infor...
Yes, I am interested in Microbiology analytical review.
I have a strong background in microbiology and enjoy analyzing data in this field.
I have experience conducting microbiological tests and interpreting the results.
I am familiar with various microbiological techniques and methodologies.
I am interested in staying updated with the latest advancements in microbiology research.
I believe that my knowledge and skills in mi...
Purified water specification refers to the set of requirements and standards that purified water must meet.
Purified water should have a low level of impurities, such as minerals, chemicals, and microorganisms.
It should meet the specifications outlined by regulatory bodies, such as the United States Pharmacopeia (USP) or European Pharmacopoeia (EP).
The pH level of purified water should be within a specific range, typica...
The purified water specification for microbial quality assurance.
Microbial specification for purified water is crucial to ensure its safety and suitability for use.
The specification typically includes limits for various microorganisms, such as bacteria, fungi, and endotoxins.
Commonly used tests for microbial quality assessment include total viable count, microbial identification, and endotoxin testing.
The specification...
Validation is the process of evaluating a system or component during or at the end of the development process to determine whether it satisfies specified requirements.
Functional Validation: Ensuring that the system meets the functional requirements.
Performance Validation: Verifying that the system performs as expected under different load conditions.
Security Validation: Checking the system for vulnerabilities and ensur...
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