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90+ Kusum Healthcare Interview Questions and Answers

Updated 15 Dec 2024

Q1. Production department Clean room experience in clean room 4years

Ans.

Yes, I have 4 years of experience working in a clean room environment in the production department.

  • I have experience working with clean room protocols and procedures.

  • I am familiar with maintaining a sterile environment and following strict hygiene practices.

  • I have experience working with specialized equipment and tools used in clean room environments.

  • I am able to work efficiently and effectively in a clean room environment, ensuring high quality production standards are met.

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Q2. What is end point of Granulation

Ans.

The end point of granulation is the formation of granules or aggregates.

  • Granulation is a process in which small particles are gathered together to form larger granules.

  • The end point is reached when the desired size and characteristics of the granules are achieved.

  • Granulation can be used in various industries such as pharmaceuticals, food processing, and chemical manufacturing.

  • For example, in pharmaceutical manufacturing, granulation is used to create tablets by compressing gr...read more

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Q3. Plz tell me Ur selp And total experience in production dept

Ans.

I have extensive experience in the production department and can contribute to the success of the organization.

  • I have worked in the production department for 10 years.

  • During my tenure, I successfully implemented lean manufacturing principles, resulting in a 20% increase in productivity.

  • I have managed a team of 50 employees and consistently met production targets.

  • I have experience in implementing quality control measures to ensure product excellence.

  • I have a track record of re...read more

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Q4. Handling air filter control air filters

Ans.

Air filter control is crucial for maintaining air quality. Proper handling is necessary to ensure optimal performance.

  • Regularly inspect and replace air filters as needed

  • Follow manufacturer's instructions for installation and maintenance

  • Ensure proper fit and seal to prevent air leaks

  • Monitor air quality and adjust filter control as necessary

  • Train personnel on proper handling and maintenance procedures

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Q5. How to do Blend Division of Granulation

Ans.

Blend division of granulation involves the process of mixing different granules to create a homogeneous mixture.

  • Blend division of granulation is a common technique used in pharmaceutical manufacturing.

  • It involves blending different granules or powders to ensure uniform distribution of active ingredients.

  • The process typically includes steps such as weighing, mixing, and sieving to achieve the desired blend.

  • Examples of blend division of granulation include the production of tab...read more

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Q6. What is the difference between Qualification and Validation

Ans.

Qualification is the process of ensuring that equipment or systems are designed and installed correctly. Validation is the process of ensuring that equipment or systems consistently produce results that meet predetermined specifications.

  • Qualification ensures that equipment or systems are designed and installed correctly

  • Validation ensures that equipment or systems consistently produce results that meet predetermined specifications

  • Qualification is done before validation

  • Qualific...read more

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Q7. How to fix drying time during validation,

Ans.

Optimize environmental conditions and equipment to reduce drying time during validation.

  • Evaluate the current environmental conditions and equipment used for drying.

  • Identify any factors that may be contributing to longer drying times.

  • Make necessary adjustments to optimize the drying process.

  • Consider using alternative drying methods or equipment if necessary.

  • Perform regular monitoring and testing to ensure consistent and efficient drying times.

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Q8. What is difference FBD and FBP

Ans.

FBD stands for Functional Block Diagram, while FBP stands for Functional Block Programming.

  • FBD is a graphical representation of a system using blocks and arrows to show the flow of signals.

  • FBP is a programming paradigm where the system is represented as a network of reusable components called black boxes.

  • FBD is commonly used in industrial automation and control systems.

  • FBP allows for modular and reusable software development.

  • FBD focuses on the physical connections between com...read more

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Q9. What is Calibration? and Tell me about Calibration of Moisture analyser,Analytical Balance And Desintegration Test apparatus.

Ans.

Calibration is the process of adjusting and verifying the accuracy of measuring instruments to ensure they provide correct results.

  • Calibration of moisture analyser involves checking the accuracy of the instrument by comparing its readings to known standards.

  • Calibration of analytical balance includes adjusting the balance to ensure it accurately measures the weight of substances.

  • Calibration of disintegration test apparatus involves verifying that the apparatus correctly measur...read more

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Q10. What are the inprocess checks during Granulation, compression, coating and packing

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Q11. How to do Yield Calculation

Ans.

Yield calculation involves determining the return on investment for a financial instrument or asset.

  • Yield calculation is used to assess the profitability of an investment.

  • It takes into account factors such as the initial investment, periodic cash flows, and the time period.

  • Different types of yield calculations include current yield, yield to maturity, and yield on cost.

  • Yield can be calculated for various financial instruments like bonds, stocks, and mutual funds.

  • For example, ...read more

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Q12. How to do Yield Recosiliation

Ans.

Yield reconciliation is the process of comparing expected and actual yields to identify discrepancies.

  • Gather data on expected yields and actual yields

  • Calculate the variance between the expected and actual yields

  • Investigate the reasons for discrepancies, such as measurement errors or process inefficiencies

  • Implement corrective actions to address the discrepancies

  • Monitor and track the effectiveness of the corrective actions

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Q13. What is the challenges in Bottle tablet/capsule filling Machine? Which was the sensor for tablet counting in BFM?

Ans.

Challenges in bottle tablet/capsule filling machine include accuracy, speed, and maintenance. The sensor for tablet counting in BFM is typically an optical sensor.

  • Accuracy of tablet/capsule counting

  • Speed of filling process

  • Maintenance of the machine

  • Optical sensor commonly used for tablet counting

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Q14. What is profibus cable it's use

Ans.

Profibus cable is a type of communication cable used in industrial automation systems.

  • Profibus cable is used to connect devices in a Profibus network, which is a widely used fieldbus communication system in industrial automation.

  • It is used to transmit data between devices such as programmable logic controllers (PLCs), sensors, actuators, and other automation components.

  • Profibus cable is designed to withstand harsh industrial environments and provide reliable communication ove...read more

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Q15. What is CAPA and how to verify the CAPA effectiveness

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Q16. What is FBD fuction

Ans.

FBD stands for Function Block Diagram, a graphical programming language used in industrial automation.

  • FBD is used to represent the logic of a control system using graphical blocks and connections.

  • It is commonly used in programmable logic controllers (PLCs) to design and implement automation processes.

  • Each block in an FBD represents a specific function or operation, and the connections between blocks define the flow of data and control signals.

  • FBD allows for easy visualization...read more

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Q17. What is RMG fuction

Ans.

RMG function refers to Resource Management Group function.

  • RMG function is responsible for managing and allocating resources within an organization.

  • It involves strategic planning, recruitment, training, and development of employees.

  • RMG function ensures that the right people with the right skills are available at the right time.

  • It also involves workforce planning, performance management, and employee engagement.

  • RMG function plays a crucial role in optimizing resource utilizatio...read more

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Q18. How to handle critical products?

Ans.

Critical products should be handled with care and attention to detail to ensure quality and safety.

  • Establish clear protocols and procedures for handling critical products

  • Train employees on proper handling techniques and safety precautions

  • Implement quality control measures to monitor the handling process

  • Regularly inspect and maintain equipment used for handling critical products

  • Have contingency plans in place for emergencies or unexpected events

  • Examples: Pharmaceuticals, medic...read more

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Q19. What is End point of Granulation? and What is End point of Drying?

Ans.

The end point of granulation is when the desired particle size distribution is achieved. The end point of drying is when the moisture content reaches the specified level.

  • Granulation end point is determined by particle size distribution

  • Drying end point is reached when moisture content meets specifications

  • Examples: Granulation end point - achieving uniform particle size distribution, Drying end point - moisture content of 2% achieved

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Q20. What is serialization? what is Mean by GTIN and What it contains?

Ans.

Serialization is the process of converting an object into a stream of bytes to store or transmit data. GTIN stands for Global Trade Item Number and contains information about a product.

  • Serialization is used to convert an object into a format that can be easily stored or transmitted, such as JSON or XML.

  • GTIN is a unique identifier for products in the supply chain, typically encoded in a barcode.

  • GTIN contains information such as the manufacturer code, product code, and check di...read more

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Q21. How to handling sar for reactors

Ans.

Handling SAR for reactors involves proper monitoring, documentation, and communication.

  • Regular monitoring of SAR levels in reactors

  • Documenting SAR data accurately for future reference

  • Communicating any SAR-related issues or changes to relevant stakeholders

  • Implementing safety measures to prevent SAR exceedance

  • Training staff on SAR monitoring and handling procedures

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Q22. Handling of BPR AND ACRS

Ans.

BPR and ACRS are both important processes that require careful handling.

  • BPR (Business Process Reengineering) involves analyzing and redesigning business processes to improve efficiency and effectiveness.

  • ACRS (Asset Cost Recovery System) is a tax deduction method used to recover the cost of depreciable assets over time.

  • Both processes require careful planning and implementation to ensure success.

  • Examples of BPR include streamlining supply chain processes or automating manual ta...read more

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Q23. Have you handled any deviations and market complaint investigations

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Q24. What is pH and how to know the acid is strong or weak by the help of pH scale

Ans.

pH is a measure of acidity or alkalinity. The pH scale ranges from 0 to 14, with 7 being neutral. Lower pH indicates stronger acids.

  • pH measures the concentration of hydrogen ions in a solution

  • pH scale ranges from 0 to 14

  • A pH of 7 is considered neutral

  • Acids have pH values less than 7

  • Lower pH values indicate stronger acids

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Q25. What is physical properties of analytical Chemistry

Ans.

Physical properties in analytical chemistry refer to characteristics of substances that can be observed or measured without changing their composition.

  • Physical properties include color, odor, density, melting point, boiling point, solubility, and conductivity.

  • These properties help in identifying and characterizing substances in analytical chemistry.

  • For example, the melting point of a compound can be used to confirm its identity by comparing it to known values.

  • Another example ...read more

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Q26. What are observations given by regulatory auditors

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Q27. What are the current Good Manufacturing Practice (cGMP) guidelines?

Ans.

cGMP guidelines are regulations ensuring the quality, safety, and efficacy of pharmaceutical products.

  • cGMP guidelines are regulations set by regulatory agencies to ensure the quality, safety, and efficacy of pharmaceutical products.

  • They cover various aspects of manufacturing, including facility design, equipment maintenance, personnel training, and record-keeping.

  • Examples of cGMP requirements include proper documentation of manufacturing processes, regular equipment calibrati...read more

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Q28. What Is Hold Time and what is Hold Time sample?

Ans.

Hold time is the amount of time a call center agent puts a caller on hold. Hold time sample is a measurement of the average time callers are put on hold.

  • Hold time is the duration a caller spends waiting on hold during a call.

  • Hold time sample is a metric used to track and analyze the average hold times of callers.

  • Reducing hold time can improve customer satisfaction and efficiency in call centers.

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Q29. What is cupdepth?

Ans.

Cupdepth refers to the measurement of the depth of a cup, typically used in reference to bras or other clothing items.

  • Cupdepth is an important factor in determining the fit and comfort of a bra.

  • It is measured from the top edge of the cup to the bottom edge, along the deepest part of the cup.

  • Different cupdepths are available to accommodate different breast shapes and sizes.

  • For example, a bra with a shallow cupdepth may be more suitable for someone with a smaller bust, while a ...read more

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Q30. What is the objective of sourcing and procurement .

Ans.

The objective of sourcing and procurement is to obtain goods and services at the right quality, quantity, price, and time.

  • To identify and select reliable suppliers

  • To negotiate favorable terms and conditions

  • To ensure timely delivery of goods and services

  • To optimize costs and achieve cost savings

  • To maintain quality standards

  • To manage supplier relationships

  • To mitigate supply chain risks

  • To support organizational goals and objectives

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Q31. Handling of Block

Ans.

Handling of block refers to the process of managing and resolving obstacles or challenges in a project or task.

  • Identify the root cause of the block

  • Brainstorm potential solutions

  • Evaluate the pros and cons of each solution

  • Select the best solution and implement it

  • Monitor progress and adjust as necessary

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Q32. What is 21 CFR part 11 and what it contains

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Q33. Type of PLC available

Ans.

There are several types of PLCs available for different industrial applications.

  • Programmable Logic Controllers (PLCs) are electronic devices used to control and automate industrial processes.

  • Different types of PLCs include modular PLCs, compact PLCs, rack-mounted PLCs, and distributed PLCs.

  • Modular PLCs allow for easy expansion and customization by adding or removing modules.

  • Compact PLCs are smaller in size and suitable for applications with limited space.

  • Rack-mounted PLCs are...read more

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Q34. What is Resolution

Ans.

Resolution is the ability to distinguish between two closely spaced objects or the ability to distinguish between two closely spaced peaks in a chromatogram.

  • Resolution is a measure of the clarity or sharpness of an image or signal.

  • It is commonly used in microscopy, spectroscopy, and chromatography.

  • Resolution is determined by factors such as the wavelength of light or radiation used, the numerical aperture of the lens, and the size of the detector.

  • In microscopy, resolution ref...read more

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Q35. How to calibrate Zero balance ?

Ans.

Zero balance calibration is done by adjusting the instrument to read zero when there is no input signal.

  • Ensure the instrument is properly connected and powered on

  • Adjust the zero balance control until the instrument reads zero

  • Repeat the process multiple times to ensure accuracy

  • Perform a final check with a known reference point

  • Document the calibration process for future reference

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Q36. Selection process both injectable and OSD sections

Ans.

The selection process for injectable and OSD sections involves screening candidates based on qualifications, experience, and skills relevant to the specific section.

  • Candidates are typically screened based on their educational background in microbiology or related field.

  • Experience working in a pharmaceutical or biotech company may be preferred.

  • Skills such as knowledge of sterile techniques, aseptic processing, and microbiological testing methods are important.

  • Candidates may be...read more

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Q37. How to do the dispensing activity

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Q38. Do u belong to reddy caste

Ans.

No, caste is not relevant to my qualifications or abilities for the Junior Manager position.

  • Caste should not be a determining factor for a managerial role

  • My qualifications, skills, and experience are what make me suitable for the position

  • Focusing on caste can lead to discrimination and bias in the workplace

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Q39. Brief discussion about dissolution and HPLC

Ans.

Dissolution and HPLC are analytical techniques used in pharmaceutical industry to assess drug release and purity.

  • Dissolution is a technique used to study the rate at which a drug substance dissolves in a specific medium.

  • HPLC (High Performance Liquid Chromatography) is a technique used to separate, identify, and quantify components in a mixture.

  • Both dissolution and HPLC are important in pharmaceutical quality control to ensure drug efficacy and safety.

  • For example, dissolution ...read more

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Q40. Plc validation and why its required

Ans.

PLC validation is the process of ensuring that a programmable logic controller (PLC) is functioning correctly and meets the required specifications.

  • PLC validation is necessary to ensure the reliability and safety of automated systems.

  • It involves testing the PLC's hardware, software, and communication interfaces.

  • Validation helps identify and rectify any errors or malfunctions in the PLC.

  • It ensures that the PLC operates as intended and meets the desired performance criteria.

  • Val...read more

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Q41. Explain the about deviation

Ans.

Deviation refers to the difference or divergence from a standard or expected value.

  • Deviation can be positive (above the standard) or negative (below the standard).

  • It is commonly used in statistics to measure the spread of data points from the mean.

  • For example, if the average temperature for a city is 70 degrees Fahrenheit and one day it reaches 80 degrees, the deviation would be +10 degrees.

  • Deviation is also used in quality control to identify variations from a set standard.

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Q42. Explain the incident procedure

Ans.

Incident procedure is a set of steps to follow in case of emergencies or unexpected events.

  • Identify the type of incident and assess the severity

  • Notify the appropriate authorities or personnel

  • Secure the area and ensure the safety of individuals involved

  • Document the incident for future reference and analysis

  • Implement corrective actions to prevent similar incidents in the future

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Q43. How much length in punch ?

Ans.

The question is unclear and may be asking about the length of a punch tool or the length of a punch action.

  • Ask for clarification on whether the question is referring to the length of a punch tool or the length of a punch action.

  • Provide examples of different punch lengths to demonstrate understanding of the question.

  • Discuss the importance of having the right punch length for specific operations.

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Q44. What is tailing factor

Ans.

Tailing factor is a measure of peak asymmetry in chromatography, indicating the presence of tailing or fronting.

  • Tailing factor is calculated by dividing the distance from the peak apex to the leading edge of the peak by the distance from the peak apex to the trailing edge of the peak.

  • A tailing factor of 1 indicates a symmetrical peak, while values greater than 1 indicate tailing and values less than 1 indicate fronting.

  • Tailing can be caused by various factors such as column o...read more

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Q45. What is ALCOA , ALCOA+

Ans.

ALCOA and ALCOA+ are principles used in data integrity and quality assurance in regulated industries.

  • ALCOA stands for Attributable, Legible, Contemporaneous, Original, and Accurate, which are key elements for ensuring data integrity.

  • ALCOA+ expands on ALCOA by adding the principles of Complete, Consistent, Enduring, and Available, further enhancing data quality and reliability.

  • These principles are commonly applied in industries such as pharmaceuticals, biotechnology, and healt...read more

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Q46. Basic definitions of Dissolution, Disintegration, etc

Ans.

Dissolution is the process by which a solid substance dissolves in a liquid, while disintegration is the breaking down of a solid dosage form into smaller particles.

  • Dissolution is the process of a solid substance dissolving in a liquid to form a solution.

  • Disintegration is the breaking down of a solid dosage form into smaller particles, usually in the presence of a liquid.

  • Dissolution is important in drug absorption as it determines the rate at which a drug becomes available fo...read more

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Q47. How to over come process issues

Ans.

To overcome process issues, it is important to identify the root cause, implement corrective actions, and continuously monitor and improve the process.

  • Identify the root cause of the process issue

  • Implement corrective actions to address the root cause

  • Continuously monitor and measure the process performance

  • Regularly review and improve the process based on data-driven insights

  • Involve relevant stakeholders in the process improvement efforts

  • Document and communicate the updated proc...read more

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Q48. What is polar, non polar

Ans.

Polar and nonpolar are terms used to describe the distribution of electrons in a molecule.

  • Polar molecules have an uneven distribution of electrons, resulting in a partial positive and partial negative charge.

  • Nonpolar molecules have an even distribution of electrons, resulting in no partial charges.

  • Examples of polar molecules include water and ammonia, while examples of nonpolar molecules include oil and methane.

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Q49. What is LAF laminar flow

Ans.

LAF laminar flow stands for Laminar Air Flow, a system that directs filtered air in a continuous flow to maintain a sterile environment.

  • LAF laminar flow is commonly used in microbiology laboratories to prevent contamination of samples.

  • It works by pushing air through a HEPA filter to remove particles and then directing the clean air in a unidirectional flow over the work area.

  • This helps to create a sterile environment for working with sensitive samples or cultures.

  • LAF laminar ...read more

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Q50. Tell me about expected package?

Ans.

The expected package for the Senior Quality Executive position will depend on factors such as experience, qualifications, and industry standards.

  • The expected package will be competitive and in line with industry standards.

  • It will be based on the candidate's qualifications, experience, and skills.

  • Additional benefits such as health insurance, retirement plans, and performance bonuses may also be included.

  • The package may vary depending on the company's size, location, and financ...read more

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Q51. Describe clean room entry and exit procedure

Ans.

Clean room entry and exit procedure involves strict protocols to maintain cleanliness and prevent contamination.

  • Clean room personnel must wear appropriate attire such as gowns, gloves, and masks.

  • Before entering the clean room, personnel must go through an air shower to remove any loose particles.

  • Upon entering the clean room, personnel must follow a designated path to prevent cross-contamination.

  • Before exiting the clean room, personnel must remove their attire and go through a...read more

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Q52. Definition of dissolution and disintegration

Ans.

Dissolution is the process of dissolving a solid substance into a liquid, while disintegration is the process of breaking down a solid substance into smaller particles.

  • Dissolution involves the complete breakdown of a solid substance into a liquid, resulting in a homogenous mixture.

  • Disintegration involves the physical breakdown of a solid substance into smaller particles, but does not involve a change in chemical composition.

  • Both dissolution and disintegration are important pr...read more

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Q53. What is chromatography

Ans.

Chromatography is a laboratory technique used to separate and analyze mixtures of chemicals.

  • It involves passing a mixture through a stationary phase, which separates the components based on their physical and chemical properties.

  • The separated components can then be identified and quantified.

  • There are different types of chromatography, including gas chromatography, liquid chromatography, and ion chromatography.

  • Gas chromatography is used to separate volatile compounds, while li...read more

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Q54. Which material using punches ?

Ans.

Metal is commonly used for punching operations due to its durability and strength.

  • Metal sheets are often punched to create holes or shapes for various applications

  • Steel, aluminum, and copper are commonly punched materials in manufacturing

  • Punching is used in industries such as automotive, aerospace, and construction

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Q55. Structures of Organic compounds,

Ans.

Organic compounds have complex structures based on carbon atoms bonded with other elements and functional groups.

  • Organic compounds are made up of carbon atoms bonded with other elements such as hydrogen, oxygen, nitrogen, sulfur, and phosphorus.

  • Functional groups such as alcohols, aldehydes, ketones, carboxylic acids, and amines give organic compounds their unique properties.

  • The arrangement of atoms in organic compounds can be represented by structural formulas, condensed form...read more

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Q56. What software do you use?

Ans.

I primarily use Microsoft Excel for data analysis and reporting.

  • Microsoft Excel for data analysis

  • Quality management software for documentation and tracking

  • Statistical software for data interpretation

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Q57. What is about clean room

Ans.

A clean room is a controlled environment with low levels of pollutants such as dust, airborne microbes, and chemical vapors.

  • Clean rooms are used in industries such as pharmaceuticals, biotechnology, electronics, and aerospace.

  • The level of cleanliness is measured by the number of particles per cubic meter of air.

  • Clean room garments such as gowns, gloves, and masks are worn to prevent contamination.

  • Airlocks and HEPA filters are used to maintain the cleanliness of the room.

  • Clean...read more

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Q58. What is analytical Chemistry

Ans.

Analytical chemistry is the branch of chemistry that deals with the analysis of substances to determine their composition and properties.

  • It involves techniques such as spectroscopy, chromatography, and mass spectrometry.

  • Analytical chemistry is used in various industries such as pharmaceuticals, environmental monitoring, and food testing.

  • It plays a crucial role in quality control, research, and development processes.

  • Analytical chemists work to identify and quantify the chemica...read more

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Q59. What is meant by titration

Ans.

Titration is a technique used in chemistry to determine the concentration of a substance in a solution.

  • Titration involves slowly adding a solution of known concentration to a solution of unknown concentration until the reaction reaches its endpoint.

  • The endpoint is usually indicated by a color change or other observable change.

  • Titration is commonly used in analytical chemistry to determine the concentration of acids, bases, and other substances in a solution.

  • Examples of titrat...read more

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Q60. How manage the production

Ans.

Managing production involves coordinating resources, optimizing processes, and ensuring timely delivery of products.

  • Develop a production plan that outlines the objectives, timelines, and resource requirements.

  • Coordinate with different departments to ensure smooth workflow and efficient utilization of resources.

  • Implement quality control measures to maintain product standards.

  • Monitor production progress and make adjustments as necessary to meet deadlines.

  • Optimize production pro...read more

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Q61. How to control rejection

Ans.

To control rejection, focus on improving quality, communication, and training.

  • Implement quality control measures to identify and address root causes of rejection

  • Enhance communication between departments to prevent misunderstandings and errors

  • Provide regular training to employees to improve skills and reduce errors

  • Analyze rejection data to identify trends and implement corrective actions

  • Establish clear guidelines and expectations for suppliers to improve product quality

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Q62. what is the form 9 in pf

Ans.

Form 9 in PF is a declaration form for employees to provide their basic details and nomination for provident fund benefits.

  • Form 9 is a declaration form required by the Employees' Provident Fund Organization (EPFO) in India.

  • It is used by employees to provide their basic details such as name, address, date of birth, etc.

  • Employees also need to mention their family members' details and provide nominations for provident fund benefits.

  • Form 9 is submitted by employees when joining a...read more

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Q63. What is thereotical plate

Ans.

Theoretical plate is a hypothetical zone in a chromatographic column where separation of components occurs.

  • Theoretical plate is a concept used in chromatography to describe the efficiency of a column.

  • It is a hypothetical zone in the column where separation of components occurs.

  • It is used to calculate the number of plates in a column.

  • The more theoretical plates a column has, the better the separation of components.

  • Theoretical plates are calculated using the Van Deemter equatio...read more

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Q64. Briefly explain the Risk assessment

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Q65. What is compression?

Ans.

Compression is the process of reducing the size of a file or data to save storage space or speed up data transmission.

  • Compression reduces the size of files or data by encoding information in a more efficient way.

  • There are two types of compression: lossless compression (reversible) and lossy compression (irreversible).

  • Examples of compression algorithms include ZIP, JPEG, and MP3.

  • Compression is commonly used in data storage, transmission, and multimedia applications.

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Q66. What is sterilization

Ans.

Sterilization is a process of killing or removing all forms of life, including microorganisms and viruses, from an object or area.

  • Sterilization can be achieved through various methods such as heat, chemicals, radiation, and filtration.

  • Common examples of sterilization methods include autoclaving, ethylene oxide gas sterilization, and UV light sterilization.

  • Sterilization is crucial in medical settings to prevent the spread of infections and ensure patient safety.

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Q67. Gowning procedure in pharma.

Ans.

Gowning procedure in pharma involves wearing specific clothing to prevent contamination in cleanroom environments.

  • Gowning typically includes wearing coveralls, hairnets, gloves, masks, and shoe covers.

  • Proper gowning helps maintain the cleanliness of the environment and prevents contamination of pharmaceutical products.

  • Gowning procedures may vary depending on the specific cleanroom classification and requirements of the pharmaceutical facility.

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Q68. What is validation

Ans.

Validation is the process of ensuring that data or information is accurate, reliable, and meets the required standards.

  • Validation involves checking data for accuracy, consistency, and completeness.

  • It helps in ensuring that the data entered is valid and meets the specified criteria.

  • Validation can be done through various methods such as data validation rules, regular audits, and cross-referencing.

  • For example, in a form submission, validation may include checking if the email ad...read more

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Q69. Steam under the pressure

Ans.

Steam under pressure refers to steam that is heated beyond its boiling point while being contained in a closed system.

  • Steam under pressure is commonly used in industrial processes such as sterilization, cooking, and power generation.

  • The high pressure allows steam to reach higher temperatures, making it more effective for certain applications.

  • Examples include autoclaves used in laboratories to sterilize equipment and steam turbines in power plants for electricity generation.

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Q70. What is chemistry

Ans.

Chemistry is the study of matter, its properties, composition, and interactions.

  • Chemistry involves understanding the structure and behavior of atoms and molecules.

  • It explores how substances react with each other and the energy changes that occur during these reactions.

  • Chemistry is essential in fields such as pharmaceuticals, materials science, and environmental science.

  • Examples include studying the properties of elements on the periodic table and analyzing chemical reactions ...read more

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Q71. What is ph acid and basic

Ans.

pH is a measure of acidity or basicity of a solution, ranging from 0 (most acidic) to 14 (most basic).

  • pH below 7 indicates acidity, while pH above 7 indicates basicity

  • Pure water has a pH of 7, considered neutral

  • Common substances: lemon juice (pH 2), bleach (pH 12), stomach acid (pH 1)

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Q72. What is marginal costing?

Ans.

Marginal costing is a costing technique where only variable costs are considered in determining the cost of a product or service.

  • Marginal costing helps in decision-making by providing information on the impact of producing additional units on profit.

  • Fixed costs are not included in the cost calculation under marginal costing.

  • It is also known as variable costing or direct costing.

  • Example: If a company produces 100 units of a product and incurs variable costs of $10 per unit, th...read more

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Q73. what are ur goals

Ans.

My goal is to ensure high quality standards are met in all aspects of QA QC processes, leading to improved efficiency and customer satisfaction.

  • Implementing and maintaining quality control procedures

  • Continuous improvement of quality assurance processes

  • Training and developing team members to uphold quality standards

  • Collaborating with other departments to address quality issues

  • Achieving ISO certification for quality management systems

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Q74. What is retailer audit

Ans.

Retailer audit is a process of evaluating and assessing the performance of retail stores to ensure compliance with company standards and policies.

  • Retailer audit involves checking inventory levels, product placement, pricing accuracy, and overall store cleanliness.

  • It helps identify areas for improvement and ensure consistency in customer experience across all stores.

  • Examples of retailer audit tools include mystery shopping, store visits, and data analysis of sales reports.

  • The ...read more

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Q75. What is Change control format

Ans.

Change control format is a structured process used to manage changes to a system or project.

  • Change control format typically includes documenting the change request, assessing the impact of the change, obtaining approval, implementing the change, and documenting the outcome.

  • It helps ensure that changes are properly evaluated, approved, and implemented to minimize risks and disruptions.

  • Examples of change control formats include change request forms, change control boards, and c...read more

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Q76. How many type of sterilization

Ans.

There are several types of sterilization methods used in various industries and settings.

  • Physical sterilization methods include heat (autoclaving), radiation (UV, gamma), and filtration.

  • Chemical sterilization methods involve using chemicals like ethylene oxide or hydrogen peroxide.

  • Other methods include dry heat sterilization, steam sterilization, and gas sterilization.

  • Each method has its own advantages and limitations depending on the specific application.

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Q77. What is spectroscopy

Ans.

Spectroscopy is the study of the interaction between matter and electromagnetic radiation.

  • It involves the measurement of the absorption, emission, or scattering of electromagnetic radiation by atoms or molecules.

  • It is used in various fields such as chemistry, physics, astronomy, and even art conservation.

  • Examples include UV-Vis spectroscopy, infrared spectroscopy, and mass spectrometry.

  • Spectroscopy can be used to identify unknown substances, determine the composition of a sam...read more

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Q78. Gas chromatography principle

Ans.

Gas chromatography is a technique used to separate and analyze compounds in a gas mixture based on their interaction with a stationary phase.

  • Gas chromatography involves a sample being vaporized and injected into a column with a stationary phase.

  • Compounds in the sample interact differently with the stationary phase, causing them to separate based on their properties.

  • The separated compounds are detected as they exit the column, allowing for identification and quantification.

  • Gas...read more

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Q79. Calibration and its role

Ans.

Calibration is the process of adjusting or verifying the accuracy of measuring instruments or equipment.

  • Calibration ensures that measurements taken by instruments are accurate and reliable.

  • It involves comparing the measurements of an instrument to a known standard.

  • Calibration helps in maintaining quality control and meeting regulatory requirements.

  • Examples of calibration include calibrating thermometers, scales, pressure gauges, and pH meters.

  • Calibration is important in indus...read more

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Q80. Dispensing Raw materials handling

Ans.

Dispensing raw materials handling involves ensuring proper storage, labeling, and dispensing of ingredients used in medication preparation.

  • Raw materials must be stored in appropriate conditions to maintain their quality and potency

  • Labels must be accurate and include important information such as expiration dates and lot numbers

  • Dispensing should be done in a controlled environment to prevent contamination

  • Proper documentation and record-keeping is essential for traceability and...read more

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Q81. Safety precautions at manufacturing

Ans.

Safety precautions at manufacturing include proper training, use of personal protective equipment, regular equipment maintenance, and emergency response plans.

  • Provide comprehensive safety training to all employees

  • Ensure proper use of personal protective equipment (PPE)

  • Regularly inspect and maintain equipment to prevent accidents

  • Develop and implement emergency response plans for various scenarios

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Q82. Check chemical expiry date

Ans.

Chemical expiry date can be checked by looking at the label or packaging.

  • Check the label or packaging of the chemical for an expiry date

  • Look for any signs of degradation or changes in color/odor

  • Consult the manufacturer's guidelines or safety data sheet for expiration information

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Q83. Fish bone analsice procedure

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Q84. Atoclave principle

Ans.

Autoclave principle involves using high pressure and steam to sterilize equipment and kill microorganisms.

  • Autoclaves use high pressure to raise the boiling point of water, allowing for sterilization at temperatures above 100°C.

  • Steam is the sterilizing agent in autoclaves, penetrating materials to kill microorganisms.

  • Proper loading and placement of items in the autoclave is crucial for effective sterilization.

  • Autoclave cycles typically include heating, sterilization, and cooli...read more

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Q85. 0.1% solution preparation?

Ans.

0.1% solution is prepared by dissolving 0.1g of a substance in 100mL of solvent.

  • Dissolve 0.1g of the substance in 100mL of solvent

  • Ensure thorough mixing to achieve a uniform concentration

  • Label the solution properly with the concentration and date of preparation

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Q86. Tell about product

Ans.

Our product is a cutting-edge medical device designed to improve patient outcomes and streamline healthcare processes.

  • Utilizes advanced technology to accurately diagnose and treat medical conditions

  • Reduces the need for invasive procedures and hospital stays

  • Increases efficiency and productivity for healthcare providers

  • Example: Our product is a portable ultrasound machine that provides high-quality imaging for quick and accurate diagnosis.

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Q87. Spark test procedure

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Q88. Capa explanation

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Q89. 33kva drawing layout

Ans.

A 33kva drawing layout is a schematic diagram showing the layout of a 33kva electrical system.

  • Include details of the transformer, switchgear, distribution panels, and other components

  • Show the connections between components and the overall layout of the system

  • Label all components and provide a key for easy understanding

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Q90. Type of selas

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Q91. Reduce the leaves

Ans.

Reduce the number of employees taking leaves

  • Implement a more efficient leave management system

  • Encourage employees to plan their leaves in advance

  • Offer incentives for employees with good attendance records

  • Provide options for remote work to reduce the need for leaves

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Q92. Describe about Hplc

Ans.

HPLC is a technique used in chemistry to separate, identify, and quantify components in a mixture.

  • HPLC stands for High-Performance Liquid Chromatography.

  • It is commonly used in pharmaceutical, environmental, and forensic analysis.

  • HPLC works by passing a liquid sample through a column packed with stationary phase material.

  • Different components in the sample interact differently with the stationary phase, leading to separation.

  • The separated components are then detected and quanti...read more

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Ans.

HPLC techniques are used to separate, identify, and quantify components in a mixture.

  • HPLC stands for High Performance Liquid Chromatography.

  • It is a powerful analytical technique used in pharmaceuticals, biotechnology, and environmental testing.

  • It involves the use of a stationary phase and a mobile phase to separate and analyze components in a mixture.

  • Different types of HPLC techniques include reverse-phase, normal-phase, ion-exchange, and size-exclusion chromatography.

  • HPLC is...read more

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