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LEVIM BIOTECH LLP Production Associate Interview Questions and Answers

Updated 28 Dec 2023

LEVIM BIOTECH LLP Production Associate Interview Experiences

1 interview found

Interview experience
4
Good
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
Selected Selected

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

Round 1 - Aptitude Test 

13 questions about laboratory related aptitudes

Round 2 - One-on-one 

(1 Question)

  • Q1. Questions about your profile

Interview questions from similar companies

Interview experience
4
Good
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
Selected Selected

I applied via Naukri.com and was interviewed before Oct 2022. There were 4 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 - One-on-one 

(4 Questions)

  • Q1. How does vaccination work?
  • Q2. What is CRISPR technology?
  • Q3. Genetically modified microorganisms' examples?
  • Ans. 

    Genetically modified microorganisms are organisms whose genetic material has been altered using genetic engineering techniques.

    • Bt corn, which produces a protein toxic to certain insects

    • Golden rice, which is engineered to produce beta-carotene

    • Yeast engineered to produce insulin

    • E. coli bacteria engineered to produce human growth hormone

  • Answered by AI
  • Q4. Basics of fermentation and parts of a fermentor?
Round 3 - Aptitude Test 

General math, English proficiency, logic and reasoning

Round 4 - Technical 

(1 Question)

  • Q1. Master's degree project summary, basic biology questions

Interview Preparation Tips

Topics to prepare for Sanofi Production Associate interview:
  • Microbiology
  • Fermentation Technology
  • Biotechnology
  • Protein Purification
Interview preparation tips for other job seekers - learn/refresh dead basics, good communication is important
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
Less than 2 weeks
Result
Selected Selected

I applied via Company Website and was interviewed in Jul 2024. There was 1 interview round.

Round 1 - Technical 

(1 Question)

  • Q1. Unit operations and transport phenomena
  • Ans. 

    Unit operations and transport phenomena are essential concepts in chemical engineering, involving processes like distillation, filtration, and heat transfer.

    • Unit operations refer to individual processes in chemical engineering, such as distillation, filtration, and crystallization.

    • Transport phenomena involve the movement of mass, energy, and momentum in chemical processes.

    • Examples of transport phenomena include heat tr...

  • Answered by AI
Interview experience
3
Average
Difficulty level
Moderate
Process Duration
4-6 weeks
Result
No response

I applied via Approached by Company and was interviewed in Mar 2024. There was 1 interview round.

Round 1 - Technical 

(2 Questions)

  • Q1. What is ALCOA ++
  • Q2. What is data integrety
  • Ans. 

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

    • Ensures data is accurate and reliable

    • Prevents unauthorized access or changes to data

    • Maintains consistency of data across systems

    • Examples: checksums, encryption, access controls

  • Answered by AI

Skills evaluated in this interview

Interview experience
4
Good
Difficulty level
Easy
Process Duration
Less than 2 weeks
Result
Selected Selected

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

Round 1 - Technical 

(2 Questions)

  • Q1. Job production operator
  • Q2. Job production myself

Interview Preparation Tips

Interview preparation tips for other job seekers - Job production
Interview experience
5
Excellent
Difficulty level
Easy
Process Duration
Less than 2 weeks
Result
Selected Selected

I applied via Walk-in and was interviewed in Nov 2023. There were 2 interview rounds.

Round 1 - Resume Shortlist 
Pro Tip by AmbitionBox:
Don’t add your photo or details such as gender, age, and address in your resume. These details do not add any value.
View all tips
Round 2 - One-on-one 

(3 Questions)

  • Q1. What is your work Experience.
  • Q2. How many years in Work Experience
  • Q3. What is your Opportunity

Interview Preparation Tips

Interview preparation tips for other job seekers - 1 years Experience at Kopran Pharmaceutical.
Interview experience
5
Excellent
Difficulty level
Easy
Process Duration
Less than 2 weeks
Result
Selected Selected

I was interviewed in Oct 2023.

Round 1 - Resume Shortlist 
Pro Tip by AmbitionBox:
Properly align and format text in your resume. A recruiter will have to spend more time reading poorly aligned text, leading to high chances of rejection.
View all tips
Round 2 - HR 

(4 Questions)

  • Q1. Self Introduction
  • Ans. My name is shubham Shukla My father's name is Mr Rakesh Shukla I am belong to Arai arhauli Dhata Fatehpur up. I have to completed my b pharmacy from Chandrashekhar Singh College of pharmacy Puramufti Kaushambi Up.
  • Answered Anonymously
  • Q2. What is Tablets.
  • Ans. 

    Tablets are portable computing devices that feature a touchscreen display and are primarily used for browsing the internet, watching videos, playing games, and running various applications.

    • Tablets are similar to smartphones but with larger screens.

    • They are lightweight and easy to carry around.

    • They typically have Wi-Fi or cellular connectivity for internet access.

    • Tablets often have built-in cameras for taking photos and...

  • Answered by AI
  • Q3. Types of tablets
  • Ans. There are to types of tablets. 1 Coated tablets 2 Uncoted tablets
  • Answered Anonymously
  • Q4. What is capsule.
  • Ans. Capsule is a very small tube containing powder and liquid medicines which you swallow.
  • Answered Anonymously
Round 3 - HR 

(2 Questions)

  • Q1. Types of capsule
  • Ans. Two types of capsule 1 Soft gelatin 2 hard gelatin
  • Answered Anonymously
  • Q2. What is the Process of drug administration.
  • Ans. There are four types of drug administration A absorption D distribution M metabolism E excretion
  • Answered Anonymously

Skills evaluated in this interview

Interview experience
4
Good
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
Selected Selected

I applied via Referral and was interviewed in Sep 2022. There were 2 interview rounds.

Round 1 - Resume Shortlist 
Pro Tip by AmbitionBox:
Double-check your resume for any spelling mistakes. The recruiter may consider spelling mistakes as careless behavior or poor communication skills.
View all tips
Round 2 - Technical 

(2 Questions)

  • Q1. Issues and inprocess checks of manufacturing and packaging QMS technical skills
  • Q2. Introduction FDA APPROVAL

Interview Preparation Tips

Interview preparation tips for other job seekers - company need low cost employees if he is not having internal link
Interview experience
5
Excellent
Difficulty level
-
Process Duration
-
Result
-
Round 1 - Resume Shortlist 
Pro Tip by AmbitionBox:
Do not use an unprofessional email address such as cool_boy@email.com. It shows a lack of professionalism by the candidate.
View all tips
Round 2 - Technical 

(2 Questions)

  • Q1. Autoclave validation
  • Q2. QMS documentation

Interview Preparation Tips

Interview preparation tips for other job seekers - Read guidelines

LEVIM BIOTECH LLP Interview FAQs

How many rounds are there in LEVIM BIOTECH LLP Production Associate interview?
LEVIM BIOTECH LLP interview process usually has 3 rounds. The most common rounds in the LEVIM BIOTECH LLP interview process are Resume Shortlist, Aptitude Test and One-on-one Round.

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LEVIM BIOTECH LLP Production Associate Salary
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₹1.9 L/yr - ₹3.3 L/yr
50% less than the average Production Associate Salary in India
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