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Intas Pharmaceuticals Senior Office Executive Interview Questions and Answers

Updated 7 Apr 2023

Intas Pharmaceuticals Senior Office Executive Interview Experiences

1 interview found

Interview experience
5
Excellent
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
Selected Selected

I applied via Naukri.com and was interviewed in Mar 2023. There were 2 interview rounds.

Round 1 - Resume Shortlist 
Pro Tip by AmbitionBox:
Keep your resume crisp and to the point. A recruiter looks at your resume for an average of 6 seconds, make sure to leave the best impression.
View all tips
Round 2 - Behavioral 

(2 Questions)

  • Q1. What is the management
  • Ans. 

    Management is the process of planning, organizing, directing, and controlling resources to achieve organizational goals.

    • Management involves setting goals and objectives for the organization

    • It includes organizing resources such as people, finances, and materials

    • Directing involves leading and motivating employees to achieve goals

    • Controlling involves monitoring progress and making adjustments as necessary

    • Examples of manag...

  • Answered by AI
  • Q2. Management is the art of responsibility

Interview Preparation Tips

Interview preparation tips for other job seekers - I wish that and eagerly waiting for your response against my CV and I waiting for interview

Interview questions from similar companies

Interview experience
5
Excellent
Difficulty level
-
Process Duration
-
Result
-
Round 1 - Technical 

(6 Questions)

  • Q1. Handling of Validation
  • Ans. 

    Validation in production involves ensuring that processes and products meet quality standards.

    • Validation involves verifying that equipment, processes, and systems are operating correctly and consistently.

    • Validation also includes confirming that products meet specifications and quality standards.

    • Documentation of validation activities is essential for regulatory compliance and continuous improvement.

    • Examples of validatio...

  • Answered by AI
  • Q2. Operations of reactors, centrifuge, sparker filters, anfds, ejectors.
  • Q3. Handling of Qualifications
  • Q4. Handling of Safety permits
  • Ans. 

    Safety permits are essential for ensuring compliance with regulations and maintaining a safe work environment.

    • Safety permits are required for certain activities or equipment to ensure they meet safety standards.

    • Production officers must be familiar with the types of safety permits needed in their industry.

    • They are responsible for obtaining and renewing safety permits as needed.

    • Failure to comply with safety permit requir...

  • Answered by AI
  • Q5. Operation of Distillation
  • Ans. 

    Distillation is a process used to separate components of a liquid mixture based on differences in boiling points.

    • Distillation involves heating the liquid mixture to create vapor, then cooling the vapor to condense it back into liquid form.

    • The components with lower boiling points will vaporize first and be collected as the distillate, while the components with higher boiling points remain in the original container.

    • Commo...

  • Answered by AI
  • Q6. Handling of Deviations
  • Ans. 

    Deviations in production processes must be promptly identified, investigated, and documented to ensure product quality and compliance.

    • Deviation should be reported immediately to the appropriate personnel

    • Investigate the root cause of the deviation

    • Document all findings and actions taken

    • Implement corrective and preventive actions to prevent recurrence

    • Review and approve deviation reports before closure

  • Answered by AI
Round 2 - One-on-one 

(5 Questions)

  • Q1. Handling of CAPA
  • Ans. 

    CAPA refers to Corrective and Preventive Actions taken to address non-conformities and prevent recurrence.

    • Identify the root cause of the issue

    • Develop a corrective action plan to address the issue

    • Implement the corrective action plan

    • Monitor the effectiveness of the corrective action

    • Implement preventive actions to prevent recurrence

  • Answered by AI
  • Q2. What is DATA INTIGRIY
  • Ans. 

    Data integrity refers to the accuracy, consistency, and reliability of data throughout its lifecycle.

    • Ensuring data is accurate and reliable

    • Maintaining consistency of data

    • Preventing unauthorized access or modifications

    • Implementing data validation processes

    • Regularly backing up data to prevent loss

  • Answered by AI
  • Q3. Handling Solvents
  • Q4. Handling of Batch failures
  • Ans. 

    Batch failures should be analyzed to identify root causes and prevent future occurrences.

    • Investigate the root cause of the batch failure

    • Implement corrective actions to prevent future failures

    • Document the findings and actions taken for future reference

    • Communicate with relevant stakeholders about the batch failure and resolution

    • Conduct a review of the production process to identify potential areas for improvement

  • Answered by AI
  • Q5. Handling of Deviations
  • Ans. 

    Handling of deviations involves identifying, investigating, and resolving any deviations from standard procedures or specifications.

    • Deviation should be documented and reported immediately

    • Investigate root cause of deviation

    • Implement corrective and preventive actions

    • Review and update procedures to prevent future deviations

  • Answered by AI
Round 3 - HR 

(3 Questions)

  • Q1. Current Role and responsibilities
  • Q2. Personal information
  • Q3. Salary discussion

Interview Preparation Tips

Interview preparation tips for other job seekers - : 1. Daily activity you are handling on daily basis.
2. Safety and MSD
3.why shifting is required
4.What is the importance of blending
5 type of GMP practices you are following
6. Information from BMR
How dis lation happen
7. About MSDS
8. Why work permit system is required
9. Difference between incident and accident:
10.Work permits

*1)* What is GMP/cGMP as per your understanding? OR What do you know about GMP/cGMP?
*2)* What is Data Integrity?
Explain it with Examples.
*3)* What is Data Manipulation?
Explain with Examples.
*4)* What is meaning of Plant Capacity / Bottleneck / Equipment / Stage..?
*5)* Safety or Process Safety related to your Products.
What/Which kind of Safety Policy do you have in your current company?
*6)* ALCOA
PPE
PH
Chilled water temp
Deviation
GMP
EHS
Process
Operations
Current role and responsibilities
Solvent
Batch fail
CAPA
Validation, qualifications

Skills evaluated in this interview

Interview experience
5
Excellent
Difficulty level
Moderate
Process Duration
-
Result
Selected Selected

I applied via Company Website

Round 1 - Technical 

(2 Questions)

  • Q1. Knowledge of HPL
  • Q2. Knowledge of Trouble shooting

Interview Preparation Tips

Interview preparation tips for other job seekers - Good communication skills, knowledge of HPLC,GC and troubleshooting.
Interview experience
4
Good
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
Selected Selected

I applied via Walk-in and was interviewed in Nov 2024. There were 2 interview rounds.

Round 1 - Technical 

(1 Question)

  • Q1. Department related questions..
Round 2 - HR 

(1 Question)

  • Q1. How much hike you want..?
Interview experience
5
Excellent
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
Selected Selected

I applied via Naukri.com and was interviewed in Jul 2024. There were 2 interview rounds.

Round 1 - One-on-one 

(1 Question)

  • Q1. Job role, work experience and past work achievements
Round 2 - One-on-one 

(1 Question)

  • Q1. In person discussion with the manager on work role and vertical knowledge

Interview Preparation Tips

Interview preparation tips for other job seekers - Revise well your work experience as your CV will be thoroughly discussed by the interviewers here.
Interview experience
5
Excellent
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
No response

I applied via Walk-in and was interviewed in Aug 2024. There were 2 interview rounds.

Round 1 - Aptitude Test 

Who is the father of your natuon

Round 2 - One-on-one 

(2 Questions)

  • Q1. Gth means what?
  • Ans. 

    Gth stands for Gross Tonnage and is a measurement of a ship's total internal volume.

    • Gross Tonnage is used to calculate fees, taxes, and regulatory requirements for ships.

    • It is a measurement of the total enclosed space within a ship, including cargo holds, engine rooms, and crew quarters.

    • Gross Tonnage does not directly relate to the weight of the ship or its cargo.

    • For example, a ship with a Gross Tonnage of 50,000 may w...

  • Answered by AI
  • Q2. Why sales people are cunning?
  • Ans. 

    Sales people are often perceived as cunning due to their ability to persuade and negotiate effectively.

    • Sales people need to be strategic and persuasive in order to close deals

    • They may use tactics like mirroring, scarcity, or social proof to influence customers

    • Cunning behavior can be a result of intense competition in the sales industry

    • Some sales people may resort to manipulation or deceit to achieve their targets

  • Answered by AI

Interview Preparation Tips

Interview preparation tips for other job seekers - Please ignore
Interview experience
3
Average
Difficulty level
Easy
Process Duration
Less than 2 weeks
Result
Not Selected

I applied via Walk-in and was interviewed in Apr 2024. There was 1 interview round.

Round 1 - Technical 

(5 Questions)

  • Q1. 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.

  • Answered by AI
  • Q2. 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 o

  • Answered by AI
  • Q3. 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 appara...

  • Answered by AI
  • Q4. 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...

  • Answered by AI
  • Q5. 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

  • Answered by AI

Interview Preparation Tips

Interview preparation tips for other job seekers - Learn from what you are working because Questions depending on Youre work.

Skills evaluated in this interview

Interview experience
5
Excellent
Difficulty level
-
Process Duration
-
Result
-
Round 1 - Technical 

(2 Questions)

  • Q1. Area qualifications
  • Q2. Equipment validation
Round 2 - Technical 

(2 Questions)

  • Q1. Manufacturing process
  • Q2. Trouble shooting
Interview experience
4
Good
Difficulty level
Easy
Process Duration
Less than 2 weeks
Result
Selected Selected

I applied via Campus Placement

Round 1 - HR 

(2 Questions)

  • Q1. What is the disintegration time of uncoated table
  • Q2. What is the role of vent filter in rmg
  • Ans. 

    Vent filter in RMG plays a crucial role in preventing contamination and maintaining the required air flow.

    • Vent filter helps in maintaining the required air flow in the RMG machine.

    • It prevents contamination by filtering out dust, particles, and other impurities from entering the machine.

    • Regular maintenance and replacement of vent filters are necessary to ensure optimal performance.

    • Vent filter also helps in maintaining t...

  • Answered by AI

Interview Preparation Tips

Interview preparation tips for other job seekers - Be confident
Interview experience
5
Excellent
Difficulty level
-
Process Duration
More than 8 weeks
Result
Selected Selected

I was interviewed in Aug 2024.

Round 1 - HR 

(5 Questions)

  • Q1. Office work Me working
  • Q2. Field me working
  • Q3. Field working me kaise hoga
  • Q4. Management office
  • Q5. Staff sath working ke office se fieldwork

Interview Preparation Tips

Interview preparation tips for other job seekers - Interview

Intas Pharmaceuticals Interview FAQs

How many rounds are there in Intas Pharmaceuticals Senior Office Executive interview?
Intas Pharmaceuticals interview process usually has 2 rounds. The most common rounds in the Intas Pharmaceuticals interview process are Resume Shortlist and Behavioral.
What are the top questions asked in Intas Pharmaceuticals Senior Office Executive interview?

Some of the top questions asked at the Intas Pharmaceuticals Senior Office Executive interview -

  1. What is the managem...read more
  2. Management is the art of responsibil...read more

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Intas Pharmaceuticals Senior Office Executive Salary
based on 4 salaries
₹3.6 L/yr - ₹5.9 L/yr
34% more than the average Senior Office Executive Salary in India
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Intas Pharmaceuticals Senior Office Executive Reviews and Ratings

based on 1 review

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4.0

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