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Biological E Quality Analyst Interview Questions and Answers for Experienced

Updated 19 Nov 2018

Biological E Quality Analyst Interview Experiences for Experienced

1 interview found

Interview Preparation Tips

Round: Resume Shortlist
Experience: Raw materila sampling
Water sampling and testing.
pH and conductivty calibration.
Balance calibration.
Volumetric and standard solutin.
And other lab work.
* Good Documentaion
* Chemical Managment
* Cleanning laboratory glasswares and cleanning of laboratory.

Interview questions from similar companies

I applied via Walk-in and was interviewed in Aug 2021. There was 1 interview round.

Interview Questionnaire 

1 Question

  • Q1. What is quality
  • Ans. 

    Quality is the degree of excellence of a product or service that meets or exceeds customer expectations.

    • Quality is meeting or exceeding customer expectations

    • It is the degree of excellence of a product or service

    • It involves meeting standards and specifications

    • It is achieved through continuous improvement

    • Examples include defect-free products, timely delivery, and excellent customer service

  • Answered by AI

Interview Preparation Tips

Interview preparation tips for other job seekers - Simple and technical and like a way impression

Interview Questionnaire 

1 Question

  • Q1. LOD.SOR.sampling programs. MR
Interview experience
3
Average
Difficulty level
-
Process Duration
-
Result
-
Round 1 - HR 

(2 Questions)

  • Q1. Personal details
  • Q2. Hobbies of you good

Interview Preparation Tips

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

I applied via Walk-in and was interviewed before Aug 2022. 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 - HR 

(4 Questions)

  • Q1. Carrier plan and strategy you have made.
  • Ans. 

    I have developed a carrier plan focused on continuous learning, skill development, and networking to advance in the field of quality analysis.

    • Continuously update skills through online courses and workshops

    • Network with industry professionals to stay updated on best practices

    • Set goals for career advancement and track progress regularly

  • Answered by AI
  • Q2. Long term as well as shot term goals
  • Q3. Where you want to see yourself after 3/4 years.
  • Q4. Are you hard working or smart working be very clear what you say with appropriate justification.

Interview Preparation Tips

Interview preparation tips for other job seekers - For freshers I would likhe to say be confident while speaking and You should be very clear about your long term life goal and streatgy. Because this is kind of question which is asked in every interview. For freshers they prefer basic questions related to industry and formulations , dosage forms and instruments likhe UV, HPLC, IR, FTIR, GC. their pricipal which you will study while pursuing B.pharm or B.sc and some chemical analysis such as limit test, arsenic, pH. Hope this will help you. Best wishes for your bright future.

Interview Questionnaire 

1 Question

  • Q1. PDA and Uv detector difference
  • Ans. 

    PDA and UV detector are both used in HPLC analysis but differ in their detection mechanism.

    • PDA detector measures the entire UV-Vis spectrum of the eluent while UV detector measures at a specific wavelength.

    • PDA detector can provide more information about the sample while UV detector is more sensitive and specific.

    • PDA detector is more expensive than UV detector.

    • PDA detector is useful for detecting impurities while UV det...

  • Answered by AI
Interview experience
4
Good
Difficulty level
-
Process Duration
-
Result
-
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 

(2 Questions)

  • Q1. Introduce yourself? Related to Cv?
  • Q2. Any past work experiences?
  • Ans. 

    Yes, I have past work experiences.

    • Worked as a Quality Analyst at XYZ Company for 2 years

    • Performed quality assurance testing on software applications

    • Identified and reported bugs and issues

    • Collaborated with development team to resolve issues

    • Conducted regression testing to ensure software stability

    • Created and executed test cases and test plans

    • Participated in requirement analysis and design reviews

  • Answered by AI

Interview Preparation Tips

Interview preparation tips for other job seekers - Be confident and share your experiences.
Stay humble in conversation

I appeared for an interview in May 2017.

Interview Preparation Tips

Round: Resume Shortlist
Experience: Query in detail as mentioned in my resume
Tips: please mention thing as you know very well

Round: HR Interview
Experience: asking for previous company any why I am intended to shift to new one
Tips: give proper reason or simply growth

Skills: Accounting

Assistant Manager Interview Questions & Answers

Micro Labs user image sunilkumar anumalasetty

posted on 19 Dec 2019

I applied via Referral and was interviewed before Dec 2018. There were 3 interview rounds.

Interview Questionnaire 

3 Questions

  • Q1. How many types of ICH guidance s
  • Q2. What is the Ich limit for methanol and class of solvent
  • Ans. 

    The Ich limit for methanol is 0.6% and it is classified as a class 3 solvent.

    • The Ich limit for methanol refers to the maximum allowable amount of methanol in a pharmaceutical product.

    • The Ich limit for methanol is set at 0.6%, meaning that the concentration of methanol should not exceed 0.6% in the product.

    • Methanol is classified as a class 3 solvent according to the International Council for Harmonisation of Technical R...

  • Answered by AI
  • Q3. What is the specification limit for known impurities and unknown impurities and which guideline explains
  • Ans. 

    The specification limit for known and unknown impurities varies depending on the specific substance being tested.

    • The specification limit for known impurities is typically set by regulatory agencies or pharmacopoeias.

    • For example, the United States Pharmacopeia (USP) sets limits for known impurities in pharmaceutical substances.

    • The specification limit for unknown impurities is usually determined through method validation...

  • Answered by AI

Interview Preparation Tips

Interview preparation tips for other job seekers - Learn about whatever topics covered in Resume and go through the current trends of guidance and deficiency received from agency's
Interview experience
5
Excellent
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
Selected Selected

I applied via Referral and was interviewed before Feb 2023. There were 2 interview rounds.

Round 1 - Technical 

(4 Questions)

  • Q1. Process Validation related.
  • Ans. Description of process validation and impact
  • Answered Anonymously
  • Q2. CPP parameters description and impact on which CQA
  • Ans. 

    CPP parameters refer to Critical Process Parameters which have a significant impact on Critical Quality Attributes (CQA) in manufacturing processes.

    • CPP parameters are specific process variables that must be controlled within a certain range to ensure product quality.

    • Examples of CPP parameters include temperature, pressure, flow rate, and mixing speed.

    • The impact of CPP parameters on CQA can be seen in the final product ...

  • Answered by AI
  • Q3. Stability studies for pharmaceutical products.
  • Q4. Annual report submission procedure for usfda approved products.
  • Ans. 

    The annual report submission procedure for USFDA approved products involves compiling data on product performance, safety, and compliance with regulations.

    • Compile data on product performance, safety, and compliance with USFDA regulations

    • Submit the annual report to the USFDA within the specified deadline

    • Include information on any changes in manufacturing processes or product labeling

    • Ensure all data submitted is accurate

  • Answered by AI
Round 2 - HR 

(1 Question)

  • Q1. Reason for leaving the job
  • Ans. For better opportunity and diversity in my career.
  • Answered Anonymously

Interview Preparation Tips

Interview preparation tips for other job seekers - Gain knowledge about the pharmaceutical industries.

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