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Biodeal Pharmaceuticals Limited Quality Assurance Officer Interview Questions and Answers

Updated 8 Aug 2023

Biodeal Pharmaceuticals Limited Quality Assurance Officer Interview Experiences

1 interview found

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

I applied via Walk-in and was interviewed in Jul 2023. 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 - Aptitude Test 

Pharmacy realeted any questions

Round 3 - Technical 

(5 Questions)

  • Q1. Crosin tab details any information
  • Q2. This tab is uncoated tablets. They are mostly used in painciller relese fever. Also used in headache.
  • Q3. Nimoslide tab Cetrizine hydro cholaride
  • Q4. Telmisartam and Amlodipibe uncoated tab
  • Q5. Amlodopine and Glimpse uncoated tablet

Interview Preparation Tips

Interview preparation tips for other job seekers - Quality Assurance department

Interview questions from similar companies

Interview experience
4
Good
Difficulty level
-
Process Duration
-
Result
Selected Selected
Round 1 - Technical 

(4 Questions)

  • Q1. What is Tablet inprocess
  • Q2. Need of line clearance
  • Ans. 

    Line clearance is necessary to prevent cross-contamination and ensure product quality by verifying that the production area is clean and ready for the next batch.

    • Prevents cross-contamination between different products or batches

    • Verifies that the production area is clean and free of any residues

    • Ensures that equipment is properly sanitized before starting a new batch

    • Confirms that all materials and components are in the c

  • Answered by AI
  • Q3. Purpose of stability study
  • Ans. 

    Stability studies are conducted to evaluate the shelf life and storage conditions of a product.

    • Stability studies help determine how long a product can be stored without significant changes in quality or efficacy.

    • They are important for establishing expiration dates and storage instructions.

    • Factors such as temperature, humidity, light exposure, and packaging materials are considered in stability studies.

    • Results of stabil...

  • Answered by AI
  • Q4. What is validation
  • Ans. 

    Validation is the process of ensuring that a product or system meets the requirements and specifications set for it.

    • Validation confirms that the product meets the customer's needs and expectations

    • It involves testing the product under real-world conditions

    • Validation is often done at the end of the development process to ensure the product is ready for release

  • Answered by AI

Skills evaluated in this interview

Interview experience
4
Good
Difficulty level
-
Process Duration
-
Result
Selected Selected
Round 1 - Technical 

(4 Questions)

  • Q1. What is Tablet inprocess
  • Q2. Need of line clearance
  • Ans. 

    Line clearance is necessary to prevent cross-contamination and ensure product quality by verifying that the production area is clean and ready for the next batch.

    • Prevents cross-contamination between different products or batches

    • Verifies that the production area is clean and free of any residues

    • Ensures that equipment is properly sanitized before starting a new batch

    • Confirms that all materials and components are in the c

  • Answered by AI
  • Q3. Purpose of stability study
  • Ans. 

    Stability studies are conducted to evaluate the shelf life and storage conditions of a product.

    • Stability studies help determine how long a product can be stored without significant changes in quality or efficacy.

    • They are important for establishing expiration dates and storage instructions.

    • Factors such as temperature, humidity, light exposure, and packaging materials are considered in stability studies.

    • Results of stabil...

  • Answered by AI
  • Q4. What is validation
  • Ans. 

    Validation is the process of ensuring that a product or system meets the requirements and specifications set for it.

    • Validation confirms that the product meets the customer's needs and expectations

    • It involves testing the product under real-world conditions

    • Validation is often done at the end of the development process to ensure the product is ready for release

  • Answered by AI

Skills evaluated in this interview

I applied via Naukri.com and was interviewed in Jun 2021. There was 1 interview round.

Interview Questionnaire 

1 Question

  • Q1. Related to job profile

Interview Preparation Tips

Interview preparation tips for other job seekers - Basic knowledge in ipqa

Biodeal Pharmaceuticals Limited Interview FAQs

How many rounds are there in Biodeal Pharmaceuticals Limited Quality Assurance Officer interview?
Biodeal Pharmaceuticals Limited interview process usually has 3 rounds. The most common rounds in the Biodeal Pharmaceuticals Limited interview process are Resume Shortlist, Aptitude Test and Technical.
What are the top questions asked in Biodeal Pharmaceuticals Limited Quality Assurance Officer interview?

Some of the top questions asked at the Biodeal Pharmaceuticals Limited Quality Assurance Officer interview -

  1. This tab is uncoated tablets. They are mostly used in painciller relese fever. ...read more
  2. Crosin tab details any informat...read more
  3. Nimoslide tab Cetrizine hydro cholar...read more

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Biodeal Pharmaceuticals Limited Quality Assurance Officer Interview Process

based on 1 interview

Interview experience

4
  
Good
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Biodeal Pharmaceuticals Limited Quality Assurance Officer Reviews and Ratings

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5.0

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5.0

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4.0

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5.0

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5.0

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