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Renault-Nissan Production Trainee Interview Questions and Answers

Updated 11 Nov 2021

Renault-Nissan Production Trainee Interview Experiences

1 interview found

Interview Questionnaire 

1 Question

  • Q1. They asked about subject knowledge and they tested my communication skills and spoken English.

Interview Preparation Tips

Interview preparation tips for other job seekers - One should speak with confidence is the most important thing. Whatever you could know you should speak with confidence

Interview questions from similar companies

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

3 test were their technical, aptitude (verbal and non verbal reasoning) , human behavior.

Round 2 - Technical 

(2 Questions)

  • Q1. Regarding pre-treatment
  • Q2. Ed defects and mechanisms
Interview experience
4
Good
Difficulty level
Easy
Process Duration
2-4 weeks
Result
Selected Selected

I applied via Walk-in and was interviewed in Oct 2024. There were 5 interview rounds.

Round 1 - Aptitude Test 

Written exam with 15 to 30 minutes

Round 2 - Group Discussion 

Topic will be given or asked

Round 3 - HR 

(2 Questions)

  • Q1. Personal Interview questions
  • Q2. What do you expect in the job?
  • Ans. 

    I expect a challenging role where I can utilize my production skills to improve efficiency and quality.

    • Opportunities to implement process improvements

    • Collaboration with cross-functional teams

    • Training and development opportunities

    • Clear communication of expectations and goals

    • Support from management in achieving targets

  • Answered by AI
Round 4 - One-on-one 

(2 Questions)

  • Q1. With Manager/HOD
  • Q2. Simple Technical questions from your educational backgrounds
Round 5 - One-on-one 

(2 Questions)

  • Q1. Plant Head/ Cluster head
  • Q2. Generally asking about questions to evaluate
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
4
Good
Difficulty level
-
Process Duration
-
Result
-
Round 1 - Technical 

(1 Question)

  • Q1. What is uptime in detail

Interview Preparation Tips

Interview preparation tips for other job seekers - Technical knowledge of improvement of uptime
Interview experience
5
Excellent
Difficulty level
-
Process Duration
-
Result
-
Round 1 - Technical 

(5 Questions)

  • Q1. Tell me about DCS HMI
  • Q2. How to manage manpower &cost reduction
  • Ans. 

    Manpower can be managed by proper planning, training, and delegation. Cost reduction can be achieved through efficiency improvements, waste reduction, and negotiation with suppliers.

    • Develop a detailed manpower plan based on workload and skill requirements

    • Invest in training and development programs to upskill existing employees

    • Delegate tasks effectively to ensure optimal use of manpower

    • Implement efficiency improvements ...

  • Answered by AI
  • Q3. About documentation
  • Q4. Production planning
  • Q5. Batchprocess with safety
  • Ans. 

    Batch process with safety involves ensuring that production processes are carried out in a safe and controlled manner.

    • Implementing safety protocols and procedures for each step of the batch process

    • Regularly conducting safety audits and inspections to identify potential hazards

    • Providing proper training to employees on safety measures and emergency procedures

    • Using appropriate personal protective equipment (PPE) when hand...

  • Answered by AI

Production Manager Interview Questions & Answers

MSN Laboratories user image chilakala Venkateswara reddy

posted on 23 Jun 2024

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

Handling of trouble shooting, block maintain capabilities, processes related documents, and forms which are handled in manufacturing

Round 2 - Technical 

(3 Questions)

  • Q1. Process related impurities,
  • Q2. Safety precautions at manufacturing
  • Ans. 

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

    • Provide comprehensive safety training to all employees

    • Ensure proper use of personal protective equipment (PPE)

    • Regularly inspect and maintain equipment to prevent accidents

    • Develop and implement emergency response plans for various scenarios

  • Answered by AI
  • Q3. Achievement at career

Interview Preparation Tips

Interview preparation tips for other job seekers - Very good organization, , I am feel great
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 Apr 2024. There was 1 interview round.

Round 1 - One-on-one 

(5 Questions)

  • Q1. Mfg Machine opereating
  • Q2. Production .mfg
  • Q3. Filling machine
  • Q4. Tablet Cotting department
  • Q5. Granulation department

Interview Preparation Tips

Topics to prepare for Cipla Production Operator interview:
  • Hr Fresher
Interview preparation tips for other job seekers - Fresher
Interview experience
5
Excellent
Difficulty level
Easy
Process Duration
Less than 2 weeks
Result
Selected Selected

I applied via Company Website and was interviewed in Mar 2024. There were 2 interview rounds.

Round 1 - Product Management 

(2 Questions)

  • Q1. PMR(paint mixing room),SAM( reservation, booking,PR, PO,BOM
  • Q2. Preventive maintenance,
Round 2 - Technical 

(3 Questions)

  • Q1. Production planning
  • Q2. Gun flow ret check
  • Q3. Oracle software, paint shop production
Interview experience
5
Excellent
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
Not Selected

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

Round 1 - One-on-one 

(5 Questions)

  • Q1. Disinfectant used in fumigation
  • Ans. 

    Common disinfectants used in fumigation include formaldehyde, hydrogen peroxide, and chlorine dioxide.

    • Formaldehyde is a widely used disinfectant in fumigation due to its effectiveness in killing a variety of pathogens.

    • Hydrogen peroxide is another common disinfectant used in fumigation, known for its broad spectrum antimicrobial properties.

    • Chlorine dioxide is also used in fumigation as a disinfectant, particularly for i...

  • Answered by AI
  • Q2. No of doors of autoclave
  • Ans. 

    The autoclave typically has one or two doors, depending on the design and size of the equipment.

    • Autoclaves can have either one or two doors for loading and unloading of materials.

    • Single-door autoclaves are more common in smaller models, while larger autoclaves may have two doors for easier access.

    • Having multiple doors can also allow for separate chambers within the autoclave for different sterilization processes.

  • Answered by AI
  • Q3. Parts of Schedule M
  • Q4. Which media is used in media fill validation
  • Ans. 

    The media used in media fill validation is typically a sterile growth medium.

    • Sterile growth medium is used to simulate the conditions of a real production run

    • Common media used include tryptic soy broth (TSB) or tryptic soy agar (TSA)

    • Media fill validation is important for ensuring the sterility of the production process

  • Answered by AI
  • Q5. What is aseptic filling
  • Ans. 

    Aseptic filling is a process of filling sterile products into containers under sterile conditions to prevent contamination.

    • Involves filling containers with sterile products

    • Done under sterile conditions to prevent contamination

    • Commonly used in pharmaceutical and food industries

    • Requires specialized equipment and trained personnel

  • Answered by AI

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Renault-Nissan Production Trainee Salary
based on 4 salaries
₹1.6 L/yr - ₹2.5 L/yr
At par with the average Production Trainee Salary in India
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based on 2 reviews

4.8/5

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4.8

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4.0

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