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200+ LivSYT Interview Questions and Answers

Updated 2 Jan 2025
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Q1. What are the necessary precautions to be taken while handling of the solvent in area ?

Ans.

Precautions for handling solvents in the area

  • Ensure proper ventilation in the area to prevent the buildup of fumes

  • Use appropriate personal protective equipment (PPE) such as gloves, goggles, and masks

  • Store solvents in designated containers and away from heat sources

  • Follow proper labeling and handling instructions provided by the manufacturer

  • Implement proper spill control measures and have spill kits readily available

  • Train employees on safe handling procedures and emergency re...read more

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Q2. How could you define tablets and attribute all the qualities of tablets in single defination either be in hindi or english

Ans.

Tablets are solid dosage forms that contain medicinal substances and are intended for oral administration.

  • Tablets are a popular form of medication due to their convenience and ease of use.

  • They are made by compressing a mixture of active ingredients and excipients into a solid form.

  • Tablets can be coated to make them easier to swallow and to protect the active ingredients from degradation.

  • They come in various shapes, sizes, and colors depending on the manufacturer and the medic...read more

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Q3. If Porblem found in working condition . So what to do?

Ans.

If a problem is found in working condition, it should be addressed promptly to minimize impact and ensure smooth operations.

  • Identify the problem and its root cause

  • Determine the impact of the problem on operations

  • Develop a plan to resolve the problem

  • Implement the plan and monitor its effectiveness

  • Communicate the problem and its resolution to relevant stakeholders

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Q4. How change management is being done? Explain with example.

Ans.

Change management involves planning, implementing, and monitoring changes to ensure successful outcomes.

  • Identify the need for change

  • Develop a plan for change

  • Communicate the change to stakeholders

  • Implement the change

  • Monitor and evaluate the change

  • Example: Implementing a new software system in a company

  • - Identify the need for a new system

  • - Develop a plan for implementation

  • - Communicate the change to employees and stakeholders

  • - Implement the new system

  • - Monitor and evaluate the ...read more

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Q5. What are calibration standards, and why are they important?

Ans.

Calibration standards are reference materials used to ensure accuracy and consistency of measurements in various instruments and equipment.

  • Calibration standards are used to calibrate instruments and equipment to ensure accurate and consistent measurements.

  • They provide a known reference point for comparison, helping to identify and correct any inaccuracies in the measurement process.

  • Calibration standards are important in industries such as manufacturing, healthcare, and enviro...read more

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Q6. How the training management system is being handled?

Ans.

The training management system is handled through a combination of online modules, in-person training sessions, and ongoing coaching and feedback.

  • We use a learning management system to deliver online training modules.

  • In-person training sessions are conducted by experienced trainers.

  • We provide ongoing coaching and feedback to ensure continuous improvement.

  • We regularly evaluate the effectiveness of our training programs and make adjustments as needed.

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Q7. How CAPA effectiveness check is being performed?

Ans.

CAPA effectiveness check is performed through a systematic process of evaluating the implemented corrective actions.

  • The effectiveness of the corrective actions is evaluated by comparing the actual results with the expected results.

  • The effectiveness check is performed to ensure that the root cause of the problem has been eliminated.

  • The effectiveness check is also performed to ensure that the problem does not recur.

  • The effectiveness check is documented and reviewed by the manag...read more

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Q8. In case centrifuge bag cut What do?

Ans.

In case the centrifuge bag is cut, take immediate action to prevent contamination and ensure safety.

  • Immediately stop the centrifuge and power it off.

  • Isolate the cut bag to prevent any potential contamination.

  • Wear appropriate personal protective equipment (PPE) such as gloves and a lab coat.

  • Transfer the contents of the cut bag to a new, intact bag using sterile techniques.

  • Dispose of the cut bag and any contaminated materials properly.

  • Clean and disinfect the centrifuge and surr...read more

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Q9. How many body systems available there in human body?

Ans.

There are 11 body systems in the human body.

  • The circulatory system transports blood throughout the body.

  • The respiratory system is responsible for breathing and gas exchange.

  • The digestive system processes food and absorbs nutrients.

  • The nervous system controls body functions and sends signals.

  • The skeletal system provides support and protection.

  • The muscular system allows movement and generates heat.

  • The integumentary system includes the skin, hair, and nails.

  • The endocrine system ...read more

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Q10. If your machine will be stopped in running process by any reason so what's you will be do?

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Q11. What are steps of aseptic process simulation?

Ans.

Aseptic process simulation involves several steps to ensure the sterility of a process or environment.

  • Prepare the aseptic environment by cleaning and disinfecting the area

  • Assemble and sterilize all necessary equipment and materials

  • Perform media fill or process simulation by introducing a sterile growth medium into the process

  • Monitor and document the process, including environmental conditions and personnel behavior

  • Incubate the filled containers or media to check for any micro...read more

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Q12. What are the types of pump and valves and their usage?

Ans.

Pumps and valves are used in various industries for fluid control. There are different types of pumps and valves for different applications.

  • Types of pumps: centrifugal, positive displacement, axial flow, and jet pumps

  • Types of valves: ball, gate, globe, butterfly, needle, and diaphragm valves

  • Pumps are used to move fluids from one place to another, while valves are used to control the flow of fluids

  • Centrifugal pumps are commonly used in water treatment plants, while positive di...read more

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Q13. What are the main parameters that require calibration in the pharmaceutical industry.

Ans.

Main parameters requiring calibration in pharmaceutical industry

  • Temperature: Ensuring accurate temperature control is crucial for pharmaceutical processes.

  • Pressure: Calibration of pressure gauges and sensors is essential for safety and quality.

  • Flow rate: Precise measurement of flow rates is necessary for accurate dosing of ingredients.

  • pH level: Calibration of pH meters is important for maintaining the correct acidity or alkalinity of solutions.

  • Concentration: Calibration of in...read more

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Q14. Explain with example, complaint investigation as well as event investigation procedure.

Ans.

Complaint and event investigation procedures involve thorough analysis and documentation of incidents.

  • Gather all relevant information and evidence

  • Interview witnesses and involved parties

  • Analyze the root cause of the incident

  • Document findings and recommendations for corrective action

  • Follow up to ensure corrective action is taken

  • Example: Investigating a customer complaint about a faulty product

  • Example: Investigating an employee injury on the job

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Q15. How do you ensure environmental factors don't affect calibration results,

Ans.

Environmental factors are controlled through proper maintenance, monitoring, and calibration procedures.

  • Regularly calibrate equipment to ensure accuracy despite environmental changes.

  • Maintain equipment in optimal condition to minimize impact of environmental factors.

  • Monitor environmental conditions such as temperature, humidity, and pressure during calibration.

  • Use environmental control measures such as shielding or insulation to minimize external influences.

  • Follow manufacture...read more

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Q16. What is the role of stratified sample analysis and Content uniformity test ?

Ans.

Stratified sample analysis helps ensure representative sampling, while content uniformity test ensures consistency of active ingredients in a sample.

  • Stratified sample analysis involves dividing a population into subgroups based on certain characteristics before sampling.

  • Content uniformity test is used to ensure that the amount of active ingredient in each dosage unit is consistent.

  • Both techniques are important in quality control to ensure the reliability and accuracy of test ...read more

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Q17. What is the role of disintegration test and criteria of disintegration test for tablets?

Ans.

Disintegration test is a test performed on tablets to determine the time it takes for a tablet to break down into smaller particles.

  • Disintegration test helps to ensure that the tablet will disintegrate properly in the body for effective drug release.

  • The criteria for disintegration test vary depending on the type of tablet and the intended use.

  • Common criteria include the time it takes for the tablet to disintegrate into particles smaller than a certain size, usually specified ...read more

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Q18. How many types of spray gun in wruster coater

Ans.

There are typically two types of spray guns used in wruster coaters: airless spray guns and HVLP spray guns.

  • Airless spray guns are commonly used for high production applications and can handle a wide range of coatings.

  • HVLP (High Volume Low Pressure) spray guns are known for their efficiency and reduced overspray, making them ideal for fine finishes.

  • Some wruster coaters may also use electrostatic spray guns for improved coating efficiency and uniformity.

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Q19. Explain with example, deviation management procedure.

Ans.

Deviation management procedure involves identifying, documenting, investigating, and resolving any deviations from established processes or procedures.

  • Deviation is identified and documented

  • Investigation is conducted to determine the root cause

  • Corrective and preventive actions are taken

  • Follow-up is done to ensure effectiveness

  • Examples include non-conformance reports, change control procedures, and corrective action plans

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Q20. How many types Coating tablets?

Ans.

There are several types of coating tablets used in pharmaceutical industry.

  • Film coating tablets

  • Sugar coating tablets

  • Enteric coating tablets

  • Modified-release coating tablets

  • Chewable coating tablets

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Q21. PH = - LOG INTO BASE H+ ION concentration Range of ph 1 to 6.9 acidic 6.9 to 7.1 neutral 7.1 to 14 basic

Ans.

PH is a measure of acidity or basicity of a solution. It ranges from 1 to 14, with 7 being neutral.

  • PH = - log into base H+ ion concentration

  • Range of PH: 1 to 6.9 acidic, 6.9 to 7.1 neutral, 7.1 to 14 basic

  • Acidic solutions have a higher concentration of H+ ions, while basic solutions have a higher concentration of OH- ions

  • PH is important in many fields, including chemistry, biology, and environmental science

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Q22. What is your AIM. What you want to achive in pharma line.

Ans.

My aim is to contribute to the growth and success of the pharmaceutical industry by leveraging my skills and knowledge in a managerial role.

  • To lead a team of professionals and drive them towards achieving organizational goals

  • To develop and implement strategies that enhance operational efficiency and productivity

  • To ensure compliance with regulatory requirements and maintain high-quality standards

  • To foster innovation and continuous improvement in processes and products

  • To build ...read more

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Q23. What are steps of line clearance?

Ans.

Line clearance is a process of ensuring that a production line is free from any previous product, packaging material, or debris before starting a new production run.

  • Identify the production line to be cleared

  • Remove all previous products, packaging materials, and debris from the line

  • Verify that the line is clean and free from any contaminants

  • Document the line clearance process

  • Authorize the line for the next production run

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Q24. How many Batches perform in Pharma industry before comercial batch ?

Ans.

Typically, three batches are performed in the pharmaceutical industry before the commercial batch.

  • Typically, the first batch is the pilot batch, followed by the validation batch, and then the commercial batch.

  • The pilot batch is used to test the manufacturing process on a small scale before scaling up for commercial production.

  • The validation batch is used to ensure that the manufacturing process consistently produces a product that meets quality standards.

  • Once the pilot and va...read more

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Q25. What is chemistry ? What is spectroscopy?

Ans.

Chemistry is the scientific study of matter and its properties, structure, composition, and behavior.

  • Chemistry involves the study of atoms, molecules, and their interactions.

  • It is used to understand the properties and behavior of substances, and to develop new materials and technologies.

  • Examples of chemistry in everyday life include cooking, cleaning, and medicine.

  • Spectroscopy is a technique used in chemistry to study the interaction of matter with electromagnetic radiation.

  • I...read more

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Q26. What 's your knowledge for medicine , medical knowledge and usese knowledge

Ans.

I do not have medical knowledge or expertise.

  • I do not have any formal education or training in medicine.

  • I am not qualified to provide medical advice or make medical decisions.

  • If you have any medical concerns, please consult a licensed healthcare professional.

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Q27. Which parameters use in Dry Granulation? And what is the reason behind to do dry Granulation?

Ans.

Parameters used in dry granulation and reasons for its use.

  • Parameters include particle size, shape, and density of the powder material.

  • Reasons for dry granulation include avoiding use of solvents, improving flow properties, and enhancing compressibility.

  • Examples of dry granulation methods are slugging and roller compaction.

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Q28. 1. Do you know about isolators 2. Do you know about ts 3. Difference between endotoxin and pyrogen 4. Fo and fh value 5. Load pattern of autoclave. 6. What is media fill 7. Types of intervention 8. Aseptic tech...

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Q29. Disintegration and dissolution and difference between in both of them

Ans.

Disintegration refers to breaking down into smaller pieces, while dissolution refers to a substance dissolving in a solvent.

  • Disintegration is a physical process, while dissolution is a chemical process.

  • Disintegration can occur due to physical forces like heat, pressure, or mechanical action.

  • Dissolution occurs when a substance is mixed with a solvent and forms a solution.

  • Examples of disintegration include breaking a rock into smaller pieces or crushing a tablet into powder.

  • Exa...read more

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Q30. How to react a situation having you in the trouble of giving nonrealistic time line for project completion

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Q31. What is PH ? And it's Range

Ans.

pH is a measure of the acidity or alkalinity of a solution. It ranges from 0 to 14, with 7 being neutral.

  • pH stands for 'potential of hydrogen'

  • It measures the concentration of hydrogen ions in a solution

  • A pH value below 7 indicates acidity, while above 7 indicates alkalinity

  • Pure water has a pH of 7, which is considered neutral

  • Examples of pH values: lemon juice (pH 2), baking soda (pH 9), stomach acid (pH 1)

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Q32. How many types stability test in pharma? And their storage conditions ?

Ans.

There are three main types of stability tests in pharma: accelerated stability testing, long-term stability testing, and intermediate stability testing.

  • Accelerated stability testing: conducted at higher temperatures to predict the stability of a drug over a shorter period of time.

  • Long-term stability testing: conducted at recommended storage conditions to assess the stability of a drug over its entire shelf life.

  • Intermediate stability testing: conducted at intermediate conditi...read more

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Q33. What is distillation? And it's type.

Ans.

Distillation is a process of separating components of a mixture based on their boiling points.

  • It involves heating the mixture to vaporize the component with the lowest boiling point.

  • The vapor is then condensed and collected as a separate liquid.

  • Types of distillation include simple distillation, fractional distillation, and steam distillation.

  • Simple distillation is used for separating liquids with large differences in boiling points.

  • Fractional distillation is used for separati...read more

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Q34. Types of agitator in reactor and what type of flow given by different agitator

Ans.

Different types of agitators in reactors include paddle, anchor, turbine, and propeller. Each agitator provides a different type of flow such as axial, radial, or tangential flow.

  • Types of agitators include paddle, anchor, turbine, and propeller

  • Paddle agitators provide axial flow

  • Anchor agitators provide radial flow

  • Turbine agitators provide both axial and radial flow

  • Propeller agitators provide tangential flow

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Q35. on which principles does centrifugal pump work?

Ans.

Centrifugal pumps work on the principle of converting rotational kinetic energy into hydrodynamic energy.

  • The pump has an impeller that rotates and creates a centrifugal force, which pushes the fluid towards the outer edge of the impeller

  • The fluid then enters the volute casing, where the kinetic energy is converted into pressure energy

  • The pressure energy then forces the fluid out of the pump and into the piping system

  • Centrifugal pumps are commonly used in industries such as oi...read more

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Q36. Give detailing 2 - 3 products of your present company

Ans.

Our present company offers a range of pharmaceutical products for various medical conditions.

  • Product 1: XYZ - a medication for hypertension

  • Product 2: ABC - a pain reliever for moderate to severe pain

  • Product 3: PQR - a topical cream for eczema and psoriasis

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Q37. What is HPLC? What is simple distilation method?

Ans.

HPLC is a high-performance liquid chromatography technique used to separate, identify, and quantify components in a mixture.

  • HPLC uses a liquid mobile phase and a stationary phase to separate components based on their chemical properties.

  • It is commonly used in pharmaceuticals, food analysis, and environmental testing.

  • HPLC can detect and quantify very small amounts of compounds, making it a highly sensitive technique.

  • Simple distillation is a method of separating a mixture of li...read more

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Q38. How many subjects were there in Mechanical in Diploma?

Ans.

The number of subjects in Mechanical Diploma varies depending on the institution.

  • The number of subjects in Mechanical Diploma can range from 6 to 10 depending on the institution.

  • Some common subjects in Mechanical Diploma include Engineering Drawing, Mechanics, Thermodynamics, and Manufacturing Processes.

  • The exact number of subjects can be found in the curriculum or prospectus of the institution.

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Q39. What are the limitations of ohm’s law in Electric Circuit Theory?

Ans.

Ohm's law has limitations in complex circuits with non-linear components and varying conditions.

  • Ohm's law assumes linear relationship between voltage, current, and resistance, which may not hold true in all cases.

  • It does not account for non-linear components like diodes and transistors.

  • It is limited in circuits with varying conditions such as temperature, frequency, and magnetic fields.

  • Ohm's law may not be applicable in circuits with reactive components like capacitors and in...read more

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Q40. How to Manage different QC sections for timely delivery

Ans.

Effective management of QC sections requires clear communication, prioritization, and efficient allocation of resources.

  • Establish clear communication channels between QC sections and other departments

  • Prioritize tasks based on urgency and impact on overall project timeline

  • Allocate resources efficiently, taking into account workload and skill sets of team members

  • Regularly review and adjust processes to optimize efficiency and quality

  • Use project management tools to track progres...read more

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Q41. What is boiler?? & Which Types of Pump in brief??

Ans.

A boiler is a device used to generate steam or hot water for heating or power generation. There are various types of pumps used in boilers.

  • A boiler is a closed vessel that heats water or other fluids to generate steam or hot water.

  • It is commonly used in industries for heating purposes or to generate power.

  • Boilers can be classified into different types based on their design and fuel used, such as fire-tube boilers, water-tube boilers, and electric boilers.

  • Fire-tube boilers hav...read more

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Q42. How do you working for zero error?

Ans.

I ensure zero error by paying attention to detail and following a systematic approach.

  • I double-check my work to ensure accuracy

  • I follow established procedures and protocols

  • I prioritize quality over speed

  • I am open to feedback and willing to make corrections

  • I stay organized and keep track of important details

  • For example, when working on a financial report, I cross-check all the numbers and formulas to ensure accuracy before submitting the final report.

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Q43. What is process Validation?

Ans.

Process validation is the documented evidence that a process consistently produces a result meeting predetermined specifications.

  • Process validation is a quality assurance technique used to confirm that a manufacturing process consistently produces a product that meets its intended specifications.

  • It involves establishing documented evidence that the process is capable of consistently producing the desired output.

  • Process validation typically includes three stages: process desig...read more

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Q44. What is your master skill in technical?operate machines and learning to skills development.

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Q45. What size do you run in the capsule?

Ans.

The size of the capsule I run depends on the specific plant and equipment being used.

  • Capsule sizes can vary depending on the plant and equipment manufacturer.

  • Common capsule sizes include 00, 0, 1, and 2.

  • The size of the capsule can affect the dosage and efficiency of the plant operation.

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Q46. Discussion of different size problems running in capsule machine

Ans.

Different size problems in capsule machine can impact production efficiency and quality.

  • Different size capsules can lead to inconsistent dosages

  • Incorrectly sized capsules may not fit properly in packaging

  • Machine settings may need to be adjusted for different capsule sizes

  • Regular maintenance and calibration can help prevent size-related issues

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Q47. What kind of demeanor one needs to have to comply all core values?

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Q48. What is sterilization process?

Ans.

Sterilization process is a method of killing or eliminating all forms of microorganisms from a surface or object.

  • Sterilization is important in medical facilities to prevent the spread of infections.

  • Common methods of sterilization include heat, radiation, and chemical sterilants.

  • Autoclaving is a common method of sterilization that uses high pressure and steam to kill microorganisms.

  • Ethylene oxide gas is another common sterilization method used for heat-sensitive equipment.

  • Ster...read more

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Q49. Which parameters used in tablet manufacturing?

Ans.

Parameters used in tablet manufacturing include formulation, compression force, tablet hardness, disintegration time, and friability.

  • Formulation - ingredients used in the tablet

  • Compression force - pressure applied during tablet compression

  • Tablet hardness - resistance to breaking

  • Disintegration time - time taken for tablet to break down in the body

  • Friability - tendency of tablet to break or crumble

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Q50. What is quality control of the capsule?

Ans.

Quality control of the capsule involves ensuring its physical, chemical, and microbiological properties meet the required standards.

  • Physical inspection for defects, such as cracks or discoloration

  • Chemical analysis to confirm the correct composition and dosage

  • Microbiological testing to ensure the absence of harmful bacteria or fungi

  • Verification of packaging and labeling information

  • Regular monitoring and documentation of quality control processes

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Q51. What is the reason of RT variations in HPLC

Ans.

RT variations in HPLC can be caused by several factors.

  • Column temperature changes

  • Mobile phase composition changes

  • Column degradation

  • Sample matrix effects

  • Detector drift

  • Injection volume changes

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Q52. What are the requirements for including an appendix?

Ans.

An appendix should include supplementary information that is relevant but not essential to the main text.

  • The information in the appendix should be directly related to the topic of the main text.

  • It should provide additional details, data, or explanations that enhance the understanding of the main content.

  • The content in the appendix should be referenced in the main text to guide readers to it.

  • The format and style of the appendix should be consistent with the main text.

  • Appendice...read more

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Q53. Tell me the procedure before starting the process?

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Q54. What is distillation and their types?

Ans.

Distillation is a process of separating components of a mixture based on their boiling points.

  • There are two main types of distillation: batch distillation and continuous distillation.

  • Batch distillation involves separating a mixture into its components in a single batch, while continuous distillation involves a continuous feed of the mixture.

  • Other types of distillation include vacuum distillation, steam distillation, and fractional distillation.

  • Vacuum distillation is used to s...read more

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Q55. What is ER/IR dissolution acceptance criteria?

Ans.

ER/IR dissolution acceptance criteria refers to the standards used to determine the dissolution rate of extended-release and immediate-release pharmaceutical products.

  • ER/IR dissolution acceptance criteria are set by regulatory agencies to ensure the effectiveness and safety of the drug.

  • For example, the FDA may require that a certain percentage of the active ingredient is released within a specific time frame for the drug to be considered acceptable.

  • Acceptance criteria may var...read more

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Q56. Gmp means?

Ans.

GMP stands for Good Manufacturing Practice.

  • GMP is a set of guidelines and regulations that ensure the quality and safety of products during manufacturing.

  • It covers various aspects such as personnel, facilities, equipment, documentation, and processes.

  • GMP helps prevent contamination, errors, and deviations in manufacturing processes.

  • Examples of GMP requirements include proper training of personnel, maintaining clean and controlled environments, and thorough documentation of ma...read more

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Q57. What is Alcoa and explain

Ans.

Alcoa is a global leader in lightweight metals engineering and manufacturing.

  • Alcoa is a multinational corporation specializing in aluminum production and other lightweight metals.

  • The company has operations in over 10 countries and employs thousands of people worldwide.

  • Alcoa is known for its innovative technologies in aerospace, automotive, and other industries.

  • The company was founded in 1888 and has a long history of industry leadership.

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Q58. What is gas crometography?

Ans.

Gas chromatography is a technique used to separate and analyze compounds in a mixture.

  • A sample is vaporized and injected into a column filled with a stationary phase.

  • The compounds in the sample interact differently with the stationary phase and are separated as they travel through the column.

  • The separated compounds are detected and identified based on their retention time and other properties.

  • Gas chromatography is commonly used in analytical chemistry, forensics, and environm...read more

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Q59. 1. How do you review BMR and acknowledge observations to production. 2. If NVPC count occurred in filling cabinet then what will be your next step.

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Q60. How many types of excipients? And their role ?

Ans.

Excipients are inactive substances added to a drug to serve as a carrier or aid in the manufacturing process.

  • There are several types of excipients including fillers, binders, disintegrants, lubricants, and preservatives.

  • Fillers add bulk to the formulation and ensure accurate dosing.

  • Binders help hold the active ingredients together in a tablet or capsule.

  • Disintegrants promote the breakup of the tablet or capsule in the digestive tract for absorption.

  • Lubricants prevent ingredie...read more

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Q61. What is coating in tablet ? And their parameters?

Ans.

Coating in tablets refers to a layer applied to the tablet for various purposes such as taste masking, protection, or controlled release of the drug.

  • Coating helps in masking the taste of the drug, making it easier for patients to consume.

  • It provides protection to the drug from environmental factors such as moisture and light.

  • Coating can also be used for controlled release of the drug, ensuring a sustained effect over time.

  • Parameters for coating include thickness, uniformity, ...read more

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Q62. How to handle the intervention during Aseptic filling

Ans.

Interventions during aseptic filling can be handled by following strict protocols, training staff, and implementing quality control measures.

  • Establish strict protocols for aseptic filling procedures

  • Train staff on proper aseptic techniques and interventions

  • Implement quality control measures to ensure compliance

  • Regularly monitor and evaluate interventions to identify areas for improvement

  • Maintain a clean and sterile environment during aseptic filling

  • Use appropriate protective e...read more

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Q63. What is catalyst ?

Ans.

A catalyst is a substance that increases the rate of a chemical reaction without being consumed in the process.

  • Catalysts lower the activation energy required for a reaction to occur.

  • They provide an alternative reaction pathway with a lower energy barrier.

  • Catalysts can be in the form of enzymes, metals, or other substances.

  • They are not consumed or permanently changed during the reaction.

  • Examples include platinum in catalytic converters and enzymes in biological reactions.

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Q64. Why does preventive maintenance take?

Ans.

Preventive maintenance takes time to ensure equipment is functioning properly and prevent breakdowns.

  • Preventive maintenance involves inspecting and cleaning equipment to ensure it is functioning properly.

  • It also involves replacing worn or damaged parts before they cause a breakdown.

  • Regular maintenance can help prevent costly repairs and downtime.

  • Examples of preventive maintenance tasks include changing air filters, lubricating moving parts, and checking electrical connections...read more

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Q65. What you know about taxation, excise, warehouse in details.

Ans.

Taxation, excise, and warehouse are all related to the production and distribution of goods.

  • Taxation refers to the process of levying taxes on goods and services.

  • Excise is a type of tax that is levied on specific goods, such as alcohol and tobacco.

  • Warehouse refers to a storage facility where goods are kept before they are distributed.

  • Excise duty is levied on goods manufactured in India such as cigarettes, pan masala, and aerated waters.

  • Goods and Services Tax (GST) is a compre...read more

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Q66. What is CPP and CQA of tablets ?

Ans.

CPP stands for Critical Process Parameters and CQA stands for Critical Quality Attributes of tablets.

  • CPP are the key variables that must be controlled to ensure the tablet manufacturing process is successful.

  • CQA are the characteristics that are critical to the quality of the tablet and must be monitored and controlled.

  • Examples of CPP include mixing time, compression force, and drying temperature.

  • Examples of CQA include tablet hardness, dissolution rate, and content uniformity...read more

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Q67. What is the importance in print of the BMR &BPR?

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Q68. How to calculate sructural steel bar weight.

Ans.

Structural steel bar weight can be calculated using the formula: weight = (d^2/162) * L, where d is the diameter of the bar in mm and L is the length of the bar in meters.

  • Calculate the cross-sectional area of the steel bar using the formula: Area = (π * d^2) / 4, where d is the diameter of the bar in mm.

  • Determine the weight of the steel bar by multiplying the cross-sectional area by the length of the bar and the density of steel (7850 kg/m^3).

  • Weight = Area * L * 7850

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Q69. Do you know how to operate computer?

Ans.

Yes, I am proficient in operating computers for various tasks.

  • I am familiar with operating systems such as Windows and MacOS.

  • I can use software applications for data entry, analysis, and reporting.

  • I have experience troubleshooting basic computer issues.

  • I am comfortable using email, internet browsers, and Microsoft Office suite.

  • I have knowledge of keyboard shortcuts and basic computer maintenance.

Add your answer

Q70. Enlist type of utilities ?

Ans.

Utilities are services that provide essential facilities or resources for a community or organization.

  • Electricity: Provides power for lighting, heating, and operating electrical appliances.

  • Water: Supplies clean water for drinking, cooking, and sanitation purposes.

  • Gas: Used for cooking, heating, and powering certain appliances.

  • Telecommunications: Includes telephone, internet, and television services.

  • Waste Management: Deals with the collection, disposal, and recycling of waste ...read more

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Q71. Why preventive maintenance take.

Ans.

Preventive maintenance is important to ensure the efficient and reliable operation of HVAC systems.

  • Preventive maintenance helps identify and address potential issues before they become major problems.

  • Regular maintenance improves energy efficiency and reduces energy consumption.

  • It extends the lifespan of HVAC equipment and reduces the need for costly repairs or replacements.

  • Preventive maintenance ensures optimal indoor air quality and comfort for occupants.

  • It helps comply with...read more

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Q72. What is HPLC , KF, & Dissolution?

Ans.

HPLC, KF, and Dissolution are common techniques used in pharmaceutical analysis.

  • HPLC stands for High Performance Liquid Chromatography, used for separating, identifying, and quantifying components in a mixture.

  • KF refers to Karl Fischer titration, a method for measuring water content in a sample.

  • Dissolution testing is used to determine how quickly a drug dissolves in a solution, simulating its behavior in the body.

  • All three techniques are essential in pharmaceutical quality co...read more

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Q73. What is UV spectroscopy? Working theory?

Ans.

UV spectroscopy is a technique that uses ultraviolet light to measure the absorption or transmission of light by a sample.

  • UV spectroscopy is commonly used in chemistry and biochemistry to analyze the structure and purity of molecules.

  • It can be used to determine the concentration of a substance in a sample.

  • UV spectroscopy can also be used to study the kinetics of chemical reactions.

  • The working theory behind UV spectroscopy is that molecules absorb light in the UV range, causin...read more

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Q74. What is tablet DT test for not dissolved

Ans.

Tablet DT test is a test to determine the dissolution time of a tablet in a specific medium.

  • Tablet DT test is conducted to assess the time it takes for a tablet to dissolve completely in a specified medium.

  • It helps in evaluating the effectiveness of the tablet's formulation and its ability to release the active ingredient.

  • The test involves placing the tablet in a dissolution apparatus with a specific medium and monitoring the time taken for complete dissolution.

  • Results of the...read more

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Q75. Different between exhibit batch vs PPQ batches?

Ans.

Exhibit batches are used for stability studies and regulatory submissions, while PPQ batches are used for process validation.

  • Exhibit batches are manufactured for stability studies and regulatory submissions.

  • PPQ (Process Performance Qualification) batches are manufactured for process validation.

  • Exhibit batches are typically larger in size compared to PPQ batches.

  • Exhibit batches are used to demonstrate the product's stability over time.

  • PPQ batches are used to validate the manuf...read more

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Asked in
AGM Interview

Q76. what is your name mentioned in cetifiate?

Ans.

My name mentioned in certificate is John Doe.

  • My name is John Doe as mentioned in my certificate.

  • The name on my certificate is John Doe.

  • John Doe is the name mentioned on my certificate.

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Q77. What is the type A and type B ?

Ans.

Type A and Type B are personality theories that categorize individuals based on certain traits and characteristics.

  • Type A individuals are competitive, ambitious, impatient, and highly organized.

  • Type B individuals are more relaxed, laid-back, and less stressed.

  • Examples: Type A personalities may thrive in high-pressure environments like sales or finance, while Type B personalities may excel in creative fields like art or writing.

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Q78. How can you handle the document in Doc-cell?

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Q79. Management masage direct to implement in SOP floor.

Ans.

The management message to implement in SOP floor is to prioritize safety and quality in all processes.

  • Emphasize the importance of following SOPs to ensure consistency and minimize errors

  • Encourage employees to report any safety concerns or quality issues immediately

  • Provide regular training and updates on SOPs and best practices

  • Lead by example and demonstrate a commitment to safety and quality

  • Reward and recognize employees who consistently follow SOPs and contribute to a cultur...read more

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Q80. Technical competency in the field of US FDA regulatory

Ans.

I have extensive technical competency in the field of US FDA regulatory.

  • I have a deep understanding of FDA regulations and guidelines.

  • I have experience in preparing and submitting regulatory documents to the FDA.

  • I am familiar with FDA inspections and audits.

  • I stay up-to-date with changes in FDA regulations and guidelines.

  • I have successfully navigated FDA approval processes for multiple products.

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Q81. Overall strategy planning and decision making approach

Ans.

My overall strategy planning and decision making approach involves analyzing data, considering multiple perspectives, and prioritizing goals.

  • I gather and analyze data to inform my decisions

  • I consider multiple perspectives and potential outcomes

  • I prioritize goals based on their importance and feasibility

  • I communicate my decisions clearly to stakeholders

  • For example, when planning a marketing campaign, I analyze market research data, consider the target audience's preferences, p...read more

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Q82. What is sop? What effective of sop? What Do's and don't? What is DI? Like many more..

Ans.

SOP stands for Standard Operating Procedure. It is a set of step-by-step instructions compiled by an organization to help workers carry out routine operations.

  • SOP is a detailed document that outlines the procedures and processes that employees should follow in various scenarios.

  • Effective SOPs help ensure consistency, quality, and compliance in operations.

  • Do's: Clearly outline the steps, use simple language, provide examples, update regularly. Don'ts: Use vague language, skip ...read more

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Q83. What is full form of FBD

Ans.

Full form of FBD is Fluidized Bed Dryer.

  • FBD is a type of equipment used for drying solid materials by fluidizing them in a hot gas stream.

  • It is commonly used in industries such as pharmaceuticals, food processing, and chemicals.

  • Example: FBD is used in the pharmaceutical industry for drying granules and powders.

Add your answer

Q84. What is ur CTC and expectation

Ans.

Current CTC is $60,000 and expectation is $70,000.

  • Current CTC: $60,000

  • Expectation: $70,000

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Q85. Why parformance varification take?

Ans.

Performance verification takes time to ensure that the HVAC system is functioning properly and efficiently.

  • Performance verification involves testing and measuring various components of the HVAC system.

  • This process can take several hours or even days depending on the size and complexity of the system.

  • The goal is to ensure that the system is operating at peak performance and efficiency, which can save energy and reduce costs.

  • Examples of tests that may be performed include airfl...read more

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Q86. How will generate sales if customer not convinced

Ans.

By addressing their concerns and providing additional information or incentives.

  • Listen to their objections and address them with relevant information

  • Offer incentives such as discounts or free trials

  • Provide social proof through customer testimonials or case studies

  • Follow up with personalized communication to build trust

  • Create urgency with limited-time offers or scarcity tactics

Add your answer

Q87. What is media fill qualification?

Ans.

Media fill qualification is a process of testing the aseptic manufacturing process by filling sterile media into containers.

  • It is a test to ensure that the aseptic manufacturing process is working correctly.

  • It involves filling sterile media into containers to simulate the manufacturing process.

  • The filled containers are then incubated to check for any microbial growth.

  • The results of the test are used to evaluate the effectiveness of the manufacturing process and identify any a...read more

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Q88. What is pharmaceutical plant in method

Ans.

Pharmaceutical plant method refers to the processes and procedures used in the manufacturing of pharmaceutical products.

  • Pharmaceutical plant methods involve various stages such as raw material sourcing, formulation, testing, packaging, and distribution.

  • Strict adherence to Good Manufacturing Practices (GMP) is essential in pharmaceutical plant methods to ensure product quality and safety.

  • Examples of pharmaceutical plant methods include tablet compression, liquid filling, and s...read more

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Q89. Type or equipment i know how to handle

Ans.

I am proficient in handling various types of office equipment such as printers, scanners, and copiers.

  • Printers

  • Scanners

  • Copiers

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Q90. What is calibration

Ans.

Calibration is the process of adjusting or checking a device to ensure it is accurate and functioning correctly.

  • Calibration involves comparing measurements of a device to a known standard.

  • It is done to ensure accuracy and reliability of the device.

  • Calibration is important in industries like manufacturing, healthcare, and engineering.

  • Examples include calibrating thermometers, pressure gauges, and scales.

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Q91. Balance calibration ALCOA. Process of mfg Instrument calibration etc.

Ans.

ALCOA stands for Attributable, Legible, Contemporaneous, Original, and Accurate. Calibration of instruments is crucial in the manufacturing process to ensure accurate and reliable measurements.

  • ALCOA principles ensure data integrity in manufacturing processes

  • Instrument calibration is necessary to maintain accuracy and reliability

  • Regular calibration schedules should be established and followed

  • Documentation of calibration activities is essential for compliance and traceability

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Q92. What is tablet ?

Ans.

A tablet is a small, portable computer that typically has a touchscreen for input and display.

  • Portable device with touchscreen display

  • Used for various purposes like browsing, gaming, and productivity

  • Common operating systems include iOS and Android

  • Examples: iPad, Samsung Galaxy Tab, Microsoft Surface

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Q93. What's code we should using for concrete

Ans.

The code for concrete should be based on the specific project requirements and local building codes.

  • The code for concrete can vary depending on factors such as strength requirements, exposure conditions, and environmental considerations.

  • Common codes used for concrete include ACI 318 (Building Code Requirements for Structural Concrete) and ASTM C94 (Standard Specification for Ready-Mixed Concrete).

  • It is important to consult with structural engineers and local authorities to de...read more

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Q94. What are the real measures of commitments

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Q95. How do u trouble shoot batch contamination

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Q96. How to check working of Fire damper?

Ans.

Fire damper can be checked by visual inspection, drop test, and airflow test.

  • Inspect for any visible damage or obstruction

  • Perform a drop test to ensure the damper closes properly

  • Conduct an airflow test to verify the damper's ability to restrict airflow

  • Check the damper's label for installation date and maintenance schedule

  • Record the results of the inspection and tests in a logbook

Add your answer

Q97. Complete wire diagram from PID to SSR to Heaters

Ans.

The wire diagram connects the PID controller to the Solid State Relay (SSR) and then to the heaters.

  • Connect the output of the PID controller to the input of the SSR.

  • Connect the output of the SSR to the heaters.

  • Ensure proper grounding and insulation for safety.

  • Use appropriate wire gauge based on the current requirements.

  • Label all connections for easy troubleshooting.

  • Consider using color-coded wires for easy identification.

Add your answer

Q98. SOP preparation.Features of the SOP.

Ans.

SOP preparation involves creating a document that outlines the standard procedures for a particular task or process.

  • SOPs should be clear and concise

  • They should include step-by-step instructions

  • They should be regularly reviewed and updated

  • They should be easily accessible to all relevant personnel

  • Examples of SOPs include those for safety procedures, quality control, and customer service

View 1 answer

Q99. Coupling constant C-F in aromatic compounds in13 C

Ans.

Coupling constant C-F in aromatic compounds in 13C is dependent on the distance between the carbon and fluorine atoms.

  • The coupling constant is a measure of the interaction between the carbon and fluorine atoms in an aromatic compound.

  • It is influenced by the distance between the carbon and fluorine atoms, as well as the electronic environment of the molecule.

  • A larger coupling constant indicates a stronger interaction between the carbon and fluorine atoms.

  • Examples of aromatic c...read more

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Q100. What is packed bed column?

Ans.

A packed bed column is a type of chemical reactor used for separation and purification processes.

  • Consists of a cylindrical column filled with a packing material

  • Fluid is passed through the column and interacts with the packing material

  • Used in various industries such as chemical, pharmaceutical, and food processing

  • Examples include distillation columns and gas absorption columns

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