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Enaltec Labs QA Executive Interview Questions and Answers

Updated 9 Feb 2024

Enaltec Labs QA Executive Interview Experiences

1 interview found

QA Executive Interview Questions & Answers

user image Mukesh Verma

posted on 9 Feb 2024

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

I applied via Referral and was interviewed before Feb 2023. There was 1 interview round.

Round 1 - Technical 

(1 Question)

  • Q1. Describe the APQR. OOS, Process Validation. And many more
  • Ans. 

    APQR is a quality document that summarizes the results of an annual product quality review.

    • APQR stands for Annual Product Quality Review.

    • It is a quality document required by regulatory authorities.

    • APQR summarizes the results of an annual review of product quality.

    • It includes data on manufacturing processes, analytical results, complaints, deviations, and other quality-related information.

    • APQR helps identify trends, pot...

  • Answered by AI

Interview Preparation Tips

Interview preparation tips for other job seekers - No comments

Interview questions from similar companies

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

(2 Questions)

  • Q1. What are all the in process carried out in oral solids
  • Ans. 

    In the process of manufacturing oral solids, various steps are carried out to ensure quality and efficacy.

    • Raw material testing and selection

    • Granulation or blending of active ingredients and excipients

    • Compression or encapsulation of the mixture into tablets or capsules

    • Coating of tablets for protection and ease of swallowing

    • Packaging and labeling of the final product

    • Quality control testing at different stages

    • Documentatio

  • Answered by AI
  • Q2. What are cleaning validation process
  • Ans. 

    Cleaning validation process ensures that cleaning procedures effectively remove residues from equipment and surfaces.

    • Cleaning validation is a documented process to demonstrate that cleaning procedures are effective in removing residues.

    • It involves establishing acceptance criteria, selecting appropriate sampling methods, and performing analytical testing.

    • The process includes cleaning verification, which confirms that cl...

  • Answered by AI
Round 2 - HR 

(1 Question)

  • Q1. What is your positive and negative
Interview experience
4
Good
Difficulty level
-
Process Duration
-
Result
-
Round 1 - Technical 

(2 Questions)

  • Q1. Related job profile (QMS)
  • Q2. ICH guidelines
Round 2 - HR 

(1 Question)

  • Q1. Salary structure
Interview experience
4
Good
Difficulty level
-
Process Duration
-
Result
-
Round 1 - One-on-one 

(1 Question)

  • Q1. Tell me about yourself
Interview experience
5
Excellent
Difficulty level
Easy
Process Duration
-
Result
Selected Selected
Round 1 - Technical 

(2 Questions)

  • Q1. What are all the in process carried out in oral solids
  • Ans. 

    In the process of manufacturing oral solids, various steps are carried out to ensure quality and efficacy.

    • Raw material testing and selection

    • Granulation or blending of active ingredients and excipients

    • Compression or encapsulation of the mixture into tablets or capsules

    • Coating of tablets for protection and ease of swallowing

    • Packaging and labeling of the final product

    • Quality control testing at different stages

    • Documentatio

  • Answered by AI
  • Q2. What are cleaning validation process
  • Ans. 

    Cleaning validation process ensures that cleaning procedures effectively remove residues from equipment and surfaces.

    • Cleaning validation is a documented process to demonstrate that cleaning procedures are effective in removing residues.

    • It involves establishing acceptance criteria, selecting appropriate sampling methods, and performing analytical testing.

    • The process includes cleaning verification, which confirms that cl...

  • Answered by AI
Round 2 - HR 

(1 Question)

  • Q1. What is your positive and negative
Interview experience
4
Good
Difficulty level
-
Process Duration
-
Result
-
Round 1 - One-on-one 

(2 Questions)

  • Q1. Personal Details
  • Q2. Company Details
Interview experience
4
Good
Difficulty level
Easy
Process Duration
Less than 2 weeks
Result
Selected Selected

I applied via Job Portal and was interviewed in Dec 2022. There were 3 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 - Group Discussion 

Normal question related to your resume or department

Round 3 - HR 

(2 Questions)

  • Q1. Salary related and also relocate , are confirmed to joining
  • Q2. What's expected to your salary

I applied via Walk-in and was interviewed in Dec 2021. There were 4 interview rounds.

Interview Questionnaire 

5 Questions

  • Q1. 1.Define QMS In Pharma.
  • Q2. 2. Define Life Cycle of change control.
  • Ans. 

    The life cycle of change control involves planning, implementing, reviewing, and approving changes to a system or process.

    • Planning: Identify the need for change and create a plan.

    • Implementation: Make the necessary changes and document them.

    • Review: Evaluate the effectiveness of the changes and identify any issues.

    • Approval: Obtain approval from stakeholders before implementing the changes.

    • Examples: Updating software, cha...

  • Answered by AI
  • Q3. 3. Define deviation. unplanned & planned deviation with example.
  • Q4. 4. How to check Artwork . Steps. Rules.
  • Ans. 

    Artwork should be checked for accuracy and compliance with regulations.

    • Verify all text is accurate and matches the approved copy

    • Ensure all required elements are present and in the correct location

    • Check for proper color usage and consistency

    • Confirm compliance with regulatory requirements

    • Perform a final proofread for any errors or inconsistencies

  • Answered by AI
  • Q5. Guidelines for QMS, Change control, Stability, Artwork etc.
  • Ans. 

    Guidelines for QMS, change control, stability, artwork etc.

    • QMS guidelines should cover all aspects of quality management, including documentation, training, and audits.

    • Change control guidelines should outline the process for making changes to products or processes, including documentation and approval requirements.

    • Stability guidelines should cover the testing and monitoring of product stability over time, including sto...

  • Answered by AI

Interview Preparation Tips

Interview preparation tips for other job seekers - Always be confidence with your ans., they test both technical as well as communication skills. At least you have knowledge of updated guidelines for pharma.
you can explain your Ans with the help of examples.
They checked your presence of mind.

I applied via Referral and was interviewed in Dec 2020. There was 1 interview round.

Interview Questionnaire 

4 Questions

  • Q1. What is tha pH?
  • Ans. 

    pH is a measure of the acidity or alkalinity of a solution.

    • pH stands for 'potential of hydrogen'.

    • It is a logarithmic scale ranging from 0 to 14.

    • A pH of 7 is considered neutral, below 7 is acidic, and above 7 is alkaline.

    • pH is determined by the concentration of hydrogen ions in a solution.

    • Examples: Lemon juice has a pH of around 2, while baking soda has a pH of around 9.

  • Answered by AI
  • Q2. PH presens of hydrogen in sample .
  • Ans. 

    PH represents the concentration of hydrogen ions in a sample.

    • PH is measured on a scale of 0-14, with 7 being neutral.

    • A lower PH indicates higher acidity, while a higher PH indicates higher alkalinity.

    • PH can be measured using a PH meter or through chemical indicators.

    • The PH of a sample can affect its chemical properties and reactions.

  • Answered by AI
  • Q3. What is lod and difference between lod and water.
  • Ans. 

    LOD stands for Limit of Detection. It is the lowest concentration of a substance that can be reliably detected.

    • LOD is used to determine the sensitivity of an analytical method.

    • It is usually expressed as a concentration or mass.

    • Water is a chemical compound composed of hydrogen and oxygen, while LOD is a term used in analytical chemistry.

    • LOD is important in environmental testing to determine the presence of contaminants ...

  • Answered by AI
  • Q4. Lod is loss on drying to determine the volatile impurities and the water is dtermination of presens of moisture and water molecules in sample

Interview Preparation Tips

Interview preparation tips for other job seekers - Take Normally interviewe and behavior is positive then good voice .

Enaltec Labs Interview FAQs

How many rounds are there in Enaltec Labs QA Executive interview?
Enaltec Labs interview process usually has 1 rounds. The most common rounds in the Enaltec Labs interview process are Technical.
How to prepare for Enaltec Labs QA Executive interview?
Go through your CV in detail and study all the technologies mentioned in your CV. Prepare at least two technologies or languages in depth if you are appearing for a technical interview at Enaltec Labs. The most common topics and skills that interviewers at Enaltec Labs expect are Capa, Change Control, Production, Validation and API.

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Enaltec Labs QA Executive Interview Process

based on 1 interview

Interview experience

4
  
Good
View more

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Enaltec Labs QA Executive Salary
based on 4 salaries
₹4 L/yr - ₹5.7 L/yr
At par with the average QA Executive Salary in India
View more details

Enaltec Labs QA Executive Reviews and Ratings

based on 2 reviews

1.5/5

Rating in categories

1.0

Skill development

1.0

Work-life balance

1.5

Salary

1.0

Job security

1.0

Company culture

1.0

Promotions

1.0

Work satisfaction

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