Add office photos
Zydus Lifesciences logo
Engaged Employer

Zydus Lifesciences

Verified
4.1
based on 6k Reviews
Video summary
Filter interviews by
Designation
Fresher
Experienced
Clear (1)

40+ Zydus Lifesciences Interview Questions and Answers for Freshers

Updated 13 Sep 2024
Popular Designations

Q1. 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

View 1 answer
right arrow

Q2. 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

View 1 answer
right arrow

Q3. 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

Add your answer
right arrow

Q4. 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.

Add your answer
right arrow
Discover Zydus Lifesciences interview dos and don'ts from real experiences

Q5. 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

Add your answer
right arrow

Q6. 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

Add your answer
right arrow
Are these interview questions helpful?

Q7. 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

Add your answer
right arrow

Q8. 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

Add your answer
right arrow
Share interview questions and help millions of jobseekers 🌟
man with laptop

Q9. 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

Add your answer
right arrow

Q10. 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

Add your answer
right arrow

Q11. 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

Add your answer
right arrow

Q12. 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

Add your answer
right arrow

Q13. 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

Add your answer
right arrow

Q14. 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)

View 2 more answers
right arrow

Q15. 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

Add your answer
right arrow

Q16. What is density

Ans.

Density is the measure of mass per unit volume of a substance.

  • Density is calculated by dividing the mass of a substance by its volume.

  • It is a physical property that can be used to identify substances.

  • The density of a substance can change with temperature and pressure.

  • Water has a density of 1 gram per cubic centimeter.

  • The density of air is much lower than the density of water.

Add your answer
right arrow

Q17. What is Cleaning Validation?

Ans.

Cleaning validation is the process of ensuring that a cleaning procedure effectively removes residues from equipment used in the manufacturing process.

  • Cleaning validation is essential in industries such as pharmaceuticals, food and beverage, and cosmetics.

  • It involves establishing documented evidence that the cleaning process consistently removes residues to predetermined levels.

  • Validation typically includes developing a cleaning procedure, conducting cleaning trials, analyzin...read more

Add your answer
right arrow

Q18. What is Film coating?

Ans.

Film coating is a process in which a thin layer of coating material is applied to a solid dosage form to improve appearance, taste, and stability.

  • Film coating helps protect the drug from moisture, light, and air

  • It can also mask the taste of the drug to improve patient compliance

  • Examples of film-coated tablets include Advil and Tylenol

Add your answer
right arrow

Q19. 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.

View 1 answer
right arrow

Q20. 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

View 1 answer
right arrow

Q21. What is LOD ?

Ans.

LOD stands for Level of Detail. It refers to the amount of detail present in a model or visualization.

  • LOD is commonly used in computer graphics to optimize performance by displaying less detail when objects are far away.

  • It can also refer to the level of detail in data analysis, where different levels of granularity are used for different purposes.

  • For example, in a 3D video game, LOD may be used to switch between high-detail and low-detail models based on distance from the cam...read more

Add your answer
right arrow

Q22. 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

Add your answer
right arrow

Q23. 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.

View 2 more answers
right arrow

Q24. 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

View 2 more answers
right arrow

Q25. 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

View 1 answer
right arrow

Q26. 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

View 1 answer
right arrow

Q27. IP USP weight variation

Ans.

IP USP weight variation refers to the acceptable range of weight variation in a pharmaceutical product.

  • IP and USP are regulatory bodies that set standards for pharmaceutical products.

  • Weight variation refers to the acceptable range of weight difference among individual units of a product.

  • The acceptable range of weight variation depends on the type of product and its intended use.

  • For example, tablets may have a weight variation limit of +/- 5% while capsules may have a limit of...read more

Add your answer
right arrow

Q28. Type of tablet

Ans.

There are various types of tablets available in the market, including standard tablets, mini tablets, and convertible tablets.

  • Standard tablets are the most common type and come in various sizes.

  • Mini tablets are smaller in size and are more portable.

  • Convertible tablets can be used as both a tablet and a laptop.

  • Examples of popular tablets include the iPad, Samsung Galaxy Tab, and Microsoft Surface.

Add your answer
right arrow

Q29. What is Disintegration ot tablet

Ans.

Disintegration of tablet refers to the breakdown of a tablet into smaller particles when exposed to a liquid medium.

  • Disintegration is an important parameter in pharmaceutical industry to ensure the tablet will release the drug properly in the body.

  • It is typically measured in minutes and should meet the specifications set by regulatory authorities.

  • Factors affecting disintegration include formulation, manufacturing process, and storage conditions.

  • Example: A tablet disintegrates...read more

Add your answer
right arrow

Q30. 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

View 1 answer
right arrow

Q31. What is the Name of Current PM of India

Ans.

Narendra Modi is the current Prime Minister of India.

  • Narendra Modi is a member of the Bharatiya Janata Party (BJP).

  • He has been serving as the Prime Minister of India since May 2014.

  • Modi previously served as the Chief Minister of the Indian state of Gujarat from 2001 to 2014.

Add your answer
right arrow

Q32. All IPQA activities with cGMP Norms

Ans.

IPQA activities refer to In-Process Quality Assurance activities that ensure compliance with cGMP norms.

  • IPQA activities involve monitoring and inspecting the manufacturing process to ensure quality standards are met

  • Examples of IPQA activities include in-process checks, sampling, and documentation review

  • IPQA activities are essential for maintaining product quality and compliance with cGMP norms

Add your answer
right arrow

Q33. MML line operation

Ans.

MML line operation involves managing and overseeing the production process of a specific product line.

  • Ensure smooth operation of the MML line by coordinating with production staff and addressing any issues that arise

  • Monitor production output and quality to meet targets and standards

  • Implement improvements to increase efficiency and reduce waste

  • Train and develop team members to enhance their skills and performance

Add your answer
right arrow

Q34. How does temperature control?

Ans.

Temperature control is achieved through the use of HVAC systems that regulate the flow of air and heat.

  • HVAC systems use sensors to detect the temperature in a room or building

  • The system then adjusts the flow of air and heat to maintain a desired temperature

  • This is achieved through the use of thermostats, dampers, and fans

  • For example, if the temperature is too high, the system will increase the flow of cool air and decrease the flow of warm air

  • If the temperature is too low, th...read more

Add your answer
right arrow

Q35. Defect of tablet

Ans.

Defect of tablet can be due to issues in formulation, manufacturing process, or packaging.

  • Possible defects include chipping, cracking, discoloration, or improper dissolution.

  • Causes can range from incorrect ingredient ratios to inadequate compression during manufacturing.

  • Quality control measures such as visual inspection, hardness testing, and dissolution testing can help identify defects.

  • Proper storage conditions and packaging materials are also important to prevent defects.

View 1 answer
right arrow

Q36. How does RH control?

Ans.

RH control refers to the regulation of relative humidity levels in a given space.

  • RH control is important for maintaining indoor air quality and preventing mold growth.

  • It can be achieved through the use of HVAC systems, dehumidifiers, and ventilation.

  • RH levels should ideally be kept between 30-50% to ensure comfort and health.

  • Factors such as temperature, air flow, and moisture sources can affect RH levels.

  • Monitoring RH levels regularly is crucial for effective control.

View 1 answer
right arrow

Q37. Types of clean rooms?

Ans.

Clean rooms are classified based on the level of cleanliness required for specific applications.

  • Clean rooms are classified into different classes based on the maximum allowable number of particles per cubic meter of air.

  • The classification system is defined by international standards such as ISO 14644-1.

  • Some common types of clean rooms include ISO Class 1, ISO Class 5, and ISO Class 8.

  • Clean rooms are used in various industries such as pharmaceuticals, electronics, and biotechn...read more

View 2 more answers
right arrow

Q38. What is DT and Disso

Ans.

DT stands for Decision Tree, a predictive modeling technique used in machine learning. Disso likely refers to dissolution testing in pharmaceuticals.

  • DT (Decision Tree) is a supervised learning algorithm used for classification and regression tasks.

  • Decision Trees split the dataset into smaller subsets based on the most significant attribute.

  • Disso (Dissolution Testing) is a process used in pharmaceutical industry to determine how quickly a drug dissolves in a solution.

  • Dissoluti...read more

View 1 answer
right arrow

Q39. Explain Tablets

Ans.

Tablets are portable electronic devices with touchscreens used for various purposes such as browsing, gaming, and productivity.

  • Tablets are lightweight and portable, making them convenient for on-the-go use.

  • They typically have touchscreens for easy navigation and interaction.

  • Tablets can be used for a variety of purposes such as browsing the internet, playing games, watching videos, and productivity tasks.

  • Examples of popular tablets include the Apple iPad, Samsung Galaxy Tab, a...read more

Add your answer
right arrow

Q40. Formula of Water

Ans.

Chemical formula of water is H2O.

  • Chemical formula is H2O

  • Consists of 2 hydrogen atoms and 1 oxygen atom

  • Molecular weight is 18.01528 g/mol

Add your answer
right arrow

More about working at Zydus Lifesciences

Back
Awards Leaf
AmbitionBox Logo
#1 Best Pharma Company - 2021
Awards Leaf
HQ - Ahmedabad, India, India
Contribute & help others!
Write a review
Write a review
Share interview
Share interview
Contribute salary
Contribute salary
Add office photos
Add office photos

Interview Process at Zydus Lifesciences for Freshers

based on 13 interviews
Interview experience
4.0
Good
View more
interview tips and stories logo
Interview Tips & Stories
Ace your next interview with expert advice and inspiring stories

Top Interview Questions from Similar Companies

BYJU'S Logo
3.1
 • 686 Interview Questions
Mahindra & Mahindra Logo
4.1
 • 403 Interview Questions
Qualcomm Logo
3.8
 • 257 Interview Questions
Intas Pharmaceuticals Logo
4.1
 • 162 Interview Questions
FactSet Logo
3.9
 • 157 Interview Questions
Statestreet HCL Services Logo
3.3
 • 142 Interview Questions
View all
Recently Viewed
SALARIES
Zydus Lifesciences
SALARIES
Zydus Lifesciences
INTERVIEWS
Optum Global Solutions
200 top interview questions
INTERVIEWS
Zydus Lifesciences
No Interviews
INTERVIEWS
Hexaware Technologies
300 top interview questions
INTERVIEWS
Eicher Motors
No Interviews
REVIEWS
Optum Global Solutions
No Reviews
INTERVIEWS
Tata Motors
No Interviews
INTERVIEWS
Zydus Lifesciences
200 top interview questions
INTERVIEWS
Optum Global Solutions
No Interviews
Top Zydus Lifesciences Interview Questions And Answers
Share an Interview
Stay ahead in your career. Get AmbitionBox app
play-icon
play-icon
qr-code
Helping over 1 Crore job seekers every month in choosing their right fit company
75 Lakh+

Reviews

5 Lakh+

Interviews

4 Crore+

Salaries

1 Cr+

Users/Month

Contribute to help millions

Made with ❤️ in India. Trademarks belong to their respective owners. All rights reserved © 2024 Info Edge (India) Ltd.

Follow us
  • Youtube
  • Instagram
  • LinkedIn
  • Facebook
  • Twitter