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Glenmark Pharmaceuticals Quality Analyst Interview Questions, Process, and Tips
Top Glenmark Pharmaceuticals Quality Analyst Interview Questions and Answers
- Q1. What is difference between Quality Assurance and Quality control?
- Q2. What is difference between Molarity and Molality?
- Q3. What is that principle of UV- spectrophotometer?
Glenmark Pharmaceuticals Quality Analyst Interview Experiences
2 interviews found
(2 Questions)
- Q1. Why to hire you
- Q2. Why to join this company
Interview Preparation Tips
I applied via Referral and was interviewed before Nov 2019. There were 3 interview rounds.
Interview Questionnaire
7 Questions
- Q1. What is Normality?
- Ans.
Normality refers to the state of being normal or conforming to a standard or average.
Normality is a concept used in various fields to define what is considered typical or expected.
It is often used in statistics to describe the distribution of data points around a mean.
In psychology, normality refers to behavior that is within the range of what is considered socially acceptable.
Normality can also be subjective, varying ...
- Q2. What is Molarity?
- Ans.
Molarity is a measure of the concentration of a solution expressed as the number of moles of solute per liter of solution.
Molarity is calculated by dividing the number of moles of solute by the volume of the solution in liters.
It is denoted by the symbol 'M'.
Molarity is commonly used in chemistry to express the concentration of a solution.
For example, a 1 M solution of sodium chloride contains 1 mole of sodium chloride
- Q3. What is difference between Molarity and Molality?
- Ans.
Molarity is the concentration of a solution in terms of the number of moles of solute per liter of solution, while molality is the concentration of a solution in terms of the number of moles of solute per kilogram of solvent.
Molarity is denoted by M, while molality is denoted by m.
Molarity is affected by temperature changes, while molality is not.
Molarity is used in chemical reactions, while molality is used in colliga...
- Q4. What is the principle of HPLC?
- Ans.
HPLC stands for High Performance Liquid Chromatography. It is a principle used in analytical chemistry to separate, identify, and quantify components in a mixture.
HPLC uses a liquid mobile phase and a solid stationary phase to separate components based on their interactions with the stationary phase.
The principle is based on the differential partitioning of components between the mobile and stationary phases.
Components...
- Q5. What is that principle of UV- spectrophotometer?
- Ans.
The principle of UV-spectrophotometer is based on the absorption of ultraviolet (UV) light by molecules.
UV-spectrophotometer measures the absorbance of UV light by a sample.
The absorbance is directly proportional to the concentration of the absorbing species in the sample.
The principle is used in various applications such as quantitative analysis, purity determination, and kinetics studies.
UV-spectrophotometer operates...
- Q6. What is difference between Quality Assurance and Quality control?
- Ans.
Quality assurance focuses on preventing defects while quality control focuses on identifying and correcting defects.
Quality assurance is a proactive process that involves planning, designing, and implementing processes to prevent defects from occurring.
Quality control is a reactive process that involves identifying defects and taking corrective action to eliminate them.
Quality assurance is focused on the entire process...
- Q7. What is friability?
Interview Preparation Tips
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Interview questions from similar companies
Selected
I applied via Recruitment Consulltant and was interviewed in Jul 2024. There was 1 interview round.
(5 Questions)
- Q1. Types of chromatography.?
- Ans.
Chromatography is a technique used to separate and analyze mixtures of chemicals based on their properties.
Types of chromatography include gas chromatography, liquid chromatography, ion exchange chromatography, and affinity chromatography.
Gas chromatography separates compounds based on their volatility and interactions with a stationary phase.
Liquid chromatography separates compounds based on their affinity for the mob...
- Q2. Trouble shooting of HPLC and GC.?
- Ans.
Troubleshooting of HPLC and GC involves identifying and resolving issues with the equipment to ensure accurate results.
Perform regular maintenance checks on the equipment to prevent issues
Calibrate the instruments regularly to maintain accuracy
Check for leaks, blockages, or contamination in the system
Verify the integrity of columns and detectors
Review method parameters and conditions for any errors or inconsistencies
- Q3. Types Of titration.?
- Ans.
Types of titration include acid-base titration, redox titration, complexometric titration, and precipitation titration.
Acid-base titration involves the neutralization of an acid with a base or vice versa.
Redox titration involves a redox reaction between the analyte and titrant.
Complexometric titration involves the formation of a complex between the analyte and titrant.
Precipitation titration involves the formation of a
- Q4. Reverse phase and normal phase.?
- Q5. Types of HPLC and GC columns
- Ans.
Types of HPLC columns include reverse phase, normal phase, ion exchange, size exclusion, and affinity. Types of GC columns include packed, capillary, and micro-packed columns.
HPLC columns: reverse phase, normal phase, ion exchange, size exclusion, affinity
GC columns: packed, capillary, micro-packed
Interview Preparation Tips
Selected
Description the study of life
Interview Preparation Tips
I applied via Walk-in and was interviewed in Apr 2024. There was 1 interview round.
(3 Questions)
- Q1. Dissolution stages
- Q2. Acceptance value calculation for Content uniformity
- Q3. HPLC troubleshooting and column washing, preservation.
(2 Questions)
- Q1. Personal details
- Q2. Hobbies of you good
Interview Preparation Tips
Selected
I applied via Walk-in and was interviewed before Apr 2023. There was 1 interview round.
(2 Questions)
- Q1. There are so many questions like what about you know apqr bpr validation activity document activity like all.
- Q2. Than hr interview round family details why you join the intas and all.
Interview Preparation Tips
Selected
I applied via Company Website and was interviewed before Oct 2023. There was 1 interview round.
(2 Questions)
- Q1. Why you join us
- Ans.
I am passionate about ensuring quality in products and processes, and I believe in the mission and values of your company.
I have a strong background in quality assurance and a track record of improving processes and products.
I am impressed by your company's commitment to excellence and innovation.
I am excited about the opportunity to contribute to a team of talented professionals.
I believe that my skills and experience
- Q2. Describe your self
- Ans.
I am a detail-oriented Quality Analyst with a strong background in analyzing data and identifying areas for improvement.
Experienced in conducting quality assurance tests and implementing quality control procedures
Skilled in identifying defects and recommending solutions to improve product quality
Proficient in using testing tools and software to ensure product functionality
Strong communication skills to collaborate with
Interview Preparation Tips
Quality Analyst Interview Questions & Answers
Sun Pharmaceutical Industries
Anonymous
posted on 26 Jan 2023
Selected
I applied via Walk-in and was interviewed in Dec 2022. There were 3 interview rounds.
According to the field they ask questions like Chromatography, Spectroscopy etc and general introduction
They give us topic and said to discuss and give some wings for that topic
(2 Questions)
- Q1. They ask about our personal introduction in education fields and achievements and about company and salary
- Q2. What was the salary expect you as a fresher?
Interview Preparation Tips
Quality Analyst Interview Questions & Answers
Akums Drugs & Pharmaceuticals Limited
Anonymous
posted on 13 Feb 2023
I applied via Walk-in and was interviewed in Aug 2022. There were 2 interview rounds.
(2 Questions)
- Q1. WHAT IS THE STANDARD Opearating procedure of FT-IR analysis.
- Ans.
The standard operating procedure of FT-IR analysis involves sample preparation, instrument calibration, data acquisition, and interpretation.
Sample preparation involves obtaining a representative sample and preparing it for analysis.
Instrument calibration ensures accurate measurements by calibrating the instrument using known reference materials.
Data acquisition involves placing the sample in the FT-IR instrument and c...
- Q2. What is incompatibility of dosage form
- Ans. When active pharmaceutical ingredient and excipient interact each other chemically and affect the pharmacological or stability and other pharmaceutical dosage dsign problem.
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Glenmark Pharmaceuticals Quality Analyst Interview Process
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Senior Officer
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Officer
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