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Kumar Organic Products

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10+ Fincrux Technologies Interview Questions and Answers

Updated 24 Jan 2025

Q1. What is the parameterss in an Analytival method validation

Ans.

Parameters in an analytical method validation include accuracy, precision, specificity, linearity, range, and robustness.

  • Accuracy: the closeness of test results to the true value

  • Precision: the closeness of agreement between individual test results

  • Specificity: the ability to assess the analyte in the presence of other components

  • Linearity: the ability to obtain test results that are directly proportional to the analyte concentration

  • Range: the interval between the upper and lowe...read more

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Q2. When and what is the purpose of Forced degradation studies.

Ans.

Forced degradation studies are conducted to determine the stability and degradation pathways of a drug or product.

  • Forced degradation studies are performed to simulate the degradation of a drug or product under extreme conditions.

  • The purpose is to understand the degradation pathways, identify potential impurities, and evaluate the stability of the drug or product.

  • These studies help in establishing appropriate storage conditions, shelf life, and formulation strategies.

  • Forced de...read more

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Q3. How many types of Validations

Ans.

There are several types of validations used in manufacturing processes.

  • Process validation: ensuring that a manufacturing process consistently produces a product that meets predetermined quality standards.

  • Equipment validation: verifying that manufacturing equipment is properly calibrated and functioning correctly.

  • Cleaning validation: confirming that cleaning procedures effectively remove residues and contaminants from equipment.

  • Analytical method validation: validating the accu...read more

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Q4. Degradation is possible what further action

Ans.

Further action should be taken to prevent or mitigate degradation in manufacturing processes.

  • Identify the root cause of degradation

  • Implement corrective actions to address the root cause

  • Monitor and measure the effectiveness of the corrective actions

  • Continuously improve processes to prevent future degradation

  • Train and educate employees on best practices and quality standards

  • Implement preventive maintenance programs

  • Regularly inspect and maintain equipment

  • Ensure proper storage an...read more

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Q5. What activities in QMS

Ans.

Activities in QMS include establishing quality objectives, conducting audits, managing nonconformities, and continuous improvement.

  • Establishing quality objectives to ensure products meet customer requirements

  • Conducting audits to assess compliance with quality standards

  • Managing nonconformities by identifying and addressing deviations from quality requirements

  • Implementing corrective and preventive actions to prevent recurrence of issues

  • Monitoring and measuring processes to ensu...read more

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Q6. Types of process validations,

Ans.

Process validations are used to ensure that manufacturing processes consistently produce products of the desired quality.

  • There are three types of process validations: prospective, concurrent, and retrospective.

  • Prospective validation is performed before a new process is put into production.

  • Concurrent validation is performed during regular production to ensure ongoing process control.

  • Retrospective validation is performed on existing processes to confirm their consistency and ef...read more

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Q7. What a difference contamination and cross contamination

Ans.

Contamination is the presence of unwanted substances while cross-contamination is the transfer of harmful substances from one surface to another.

  • Contamination refers to the presence of unwanted substances in a particular area or on a surface.

  • Cross-contamination occurs when harmful substances are transferred from one surface to another, leading to the spread of contamination.

  • Contamination can occur due to various reasons such as poor hygiene, improper cleaning, or lack of main...read more

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Q8. What a difference differancial pressure and admoshpharic pressure

Ans.

Differential pressure is the difference between two pressures, while atmospheric pressure is the pressure exerted by the atmosphere.

  • Differential pressure is the pressure difference between two points in a system.

  • Atmospheric pressure is the pressure exerted by the Earth's atmosphere.

  • Differential pressure is used in various applications such as HVAC systems, filtration systems, and fluid flow measurement.

  • Atmospheric pressure is measured using a barometer.

  • Differential pressure c...read more

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Q9. Disinfactant Efficacy test

Ans.

Disinfectant efficacy test is performed to determine the effectiveness of a disinfectant against microorganisms.

  • The test is performed by inoculating a known concentration of microorganisms onto a surface and then treating it with the disinfectant.

  • After a specified contact time, the surface is sampled and the number of surviving microorganisms is determined.

  • The test is usually performed using a variety of microorganisms, including bacteria, fungi, and viruses.

  • The disinfectant ...read more

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Q10. What do you under about B2B sales?

Ans.

B2B sales involves selling products or services from one business to another.

  • B2B sales focus on building relationships with other businesses

  • Understanding the needs and challenges of the business you are selling to

  • Negotiating contracts and pricing tailored to the specific business

  • Utilizing data and analytics to make informed sales decisions

  • Examples: Selling software to a company for their internal use, providing marketing services to a business looking to expand

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Q11. Principles of HPLC, GC,UV-VIS,TLC

Ans.

Principles of HPLC, GC, UV-VIS, TLC involve separation of compounds based on different physical and chemical properties.

  • HPLC (High Performance Liquid Chromatography) separates compounds based on their affinity for the stationary phase and mobile phase.

  • GC (Gas Chromatography) separates compounds based on their volatility and interaction with the stationary phase.

  • UV-VIS (Ultraviolet-Visible Spectroscopy) measures the absorption of light by compounds to determine their concentra...read more

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Q12. Stores procedure

Ans.

Stores procedure involves the systematic process of managing inventory, organizing goods, and ensuring efficient operations.

  • Stores procedure includes receiving, storing, and issuing goods.

  • Inventory management is crucial to track stock levels and prevent stockouts.

  • Regular audits and stocktaking help in maintaining accurate records.

  • Proper labeling and storage of goods ensure easy retrieval and prevent damage.

  • Adherence to safety protocols and regulations is essential in stores o...read more

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