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Unichem Laboratories Quality Assurance Officer Interview Questions, Process, and Tips for Experienced

Updated 13 Aug 2023

Unichem Laboratories Quality Assurance Officer Interview Experiences for Experienced

1 interview found

Interview experience
5
Excellent
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
Selected Selected

I applied via Approached by Company and was interviewed before Aug 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.
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Round 2 - Technical 

(4 Questions)

  • Q1. What is the role of IPQA.
  • Ans. 

    IPQA stands for In-Process Quality Assurance. It involves monitoring and inspecting the quality of products during the manufacturing process.

    • IPQA ensures that products meet quality standards at every stage of production

    • It involves conducting inspections, tests, and audits to identify and address any quality issues

    • IPQA helps in preventing defects and ensuring compliance with regulations and standards

    • Examples include che...

  • Answered by AI
  • Q2. What is the ECR/BPR/BCR.
  • Ans. 

    ECR/BPR/BCR stands for Engineering Change Request/Business Process Reengineering/Business Case Reengineering.

    • ECR (Engineering Change Request) is a formal proposal to make a change to a product's design or manufacturing process.

    • BPR (Business Process Reengineering) is the analysis and redesign of workflows within and between enterprises to optimize end-to-end processes and eliminate non-value-added tasks.

    • BCR (Business Ca...

  • Answered by AI
  • Q3. How to perform area clearance or equipment clearance.
  • Ans. 

    Area or equipment clearance involves thorough cleaning and inspection to ensure safety and quality standards are met.

    • Start by removing all items from the area or equipment being cleared.

    • Clean the area or equipment using appropriate cleaning agents and tools.

    • Inspect the area or equipment for any damage, wear and tear, or contamination.

    • Document the clearance process and any findings for record-keeping purposes.

    • Ensure pro...

  • Answered by AI
  • Q4. Review point of BPR/BCR/ECR
  • Ans. 

    BPR/BCR/ECR are review points in business process management.

    • BPR stands for Business Process Reengineering, involves radical redesign of processes for improvement.

    • BCR stands for Business Continuity Review, ensures processes are in place to maintain operations during disruptions.

    • ECR stands for Engineering Change Review, evaluates proposed changes to products or processes for impact.

    • Review points help ensure efficiency,

  • Answered by AI
Round 3 - HR 

(1 Question)

  • Q1. Salary discussion and company policies

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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 May 2024. There was 1 interview round.

Round 1 - Technical 

(2 Questions)

  • Q1. Job responsibilities
  • Q2. Quality assurance questions

Interview Preparation Tips

Interview preparation tips for other job seekers - Thanks for opportunity
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Interview experience
4
Good
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
Selected Selected

I applied via Approached by Company and was interviewed in Aug 2023. There were 3 interview rounds.

Round 1 - Technical 

(5 Questions)

  • Q1. Tell me about change Control? And give me One Example?
  • Ans. 

    Change control is a process used to manage and document changes to a system or process.

    • Change control ensures that changes are properly reviewed, approved, and implemented.

    • It helps to minimize risks and ensure that changes do not negatively impact the quality or functionality of the system.

    • Change control typically involves documenting the change request, assessing its impact, obtaining necessary approvals, implementing...

  • Answered by AI
  • Q2. What are the ypes of Process validation?
  • Ans. 

    Process validation is the process of establishing documented evidence that a process consistently produces a product meeting predetermined specifications.

    • There are three types of process validation: prospective validation, concurrent validation, and retrospective validation.

    • Prospective validation is conducted before the process is put into routine use.

    • Concurrent validation is performed during routine production.

    • Retrosp...

  • Answered by AI
  • Q3. How you are doing Audit trail?
  • Ans. 

    Audit trail is maintained by documenting and tracking all activities and changes made to a system or process.

    • Audit trail is created by recording all actions, events, and transactions that occur within a system.

    • It helps in ensuring accountability, traceability, and compliance with regulations.

    • Audit trail can be established through the use of logs, timestamps, and version control.

    • It is important to capture relevant infor...

  • Answered by AI
  • Q4. Asking about APQR
  • Q5. Are you interested in Microbiology analytical review?
  • Ans. 

    Yes, I am interested in Microbiology analytical review.

    • I have a strong background in microbiology and enjoy analyzing data in this field.

    • I have experience conducting microbiological tests and interpreting the results.

    • I am familiar with various microbiological techniques and methodologies.

    • I am interested in staying updated with the latest advancements in microbiology research.

    • I believe that my knowledge and skills in mi...

  • Answered by AI
Round 2 - Technical 

(6 Questions)

  • Q1. Purified water specification?
  • Ans. 

    Purified water specification refers to the set of requirements and standards that purified water must meet.

    • Purified water should have a low level of impurities, such as minerals, chemicals, and microorganisms.

    • It should meet the specifications outlined by regulatory bodies, such as the United States Pharmacopeia (USP) or European Pharmacopoeia (EP).

    • The pH level of purified water should be within a specific range, typica...

  • Answered by AI
  • Q2. Purified water specification of Microbal
  • Ans. 

    The purified water specification for microbial quality assurance.

    • Microbial specification for purified water is crucial to ensure its safety and suitability for use.

    • The specification typically includes limits for various microorganisms, such as bacteria, fungi, and endotoxins.

    • Commonly used tests for microbial quality assessment include total viable count, microbial identification, and endotoxin testing.

    • The specification...

  • Answered by AI
  • Q3. USP chapters of Microbial tesing of API and water
  • Q4. Growth Pramotion tests
  • Q5. Horizontal Autoclave validation
  • Q6. Types of validation
  • Ans. 

    Validation is the process of evaluating a system or component during or at the end of the development process to determine whether it satisfies specified requirements.

    • Functional Validation: Ensuring that the system meets the functional requirements.

    • Performance Validation: Verifying that the system performs as expected under different load conditions.

    • Security Validation: Checking the system for vulnerabilities and ensur...

  • Answered by AI
Round 3 - HR 

(3 Questions)

  • Q1. Tell me about your self
  • Q2. Are you willing to shift Vizag
  • Q3. Salary discussion

Skills evaluated in this interview

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Interview experience
2
Poor
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
No response

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

Round 1 - HR 

(2 Questions)

  • Q1. What u know about pcr?
  • Ans. 

    PCR stands for Polymerase Chain Reaction, a technique used in molecular biology to amplify a single or a few copies of a piece of DNA.

    • PCR is a common technique used in molecular biology to make multiple copies of a specific DNA segment.

    • It involves a series of temperature changes to denature, anneal, and extend DNA strands.

    • PCR is used in various applications such as DNA sequencing, gene cloning, and genetic testing.

    • Exam...

  • Answered by AI
  • Q2. How to prepare buffer?
  • Ans. 

    Buffer preparation involves mixing a weak acid and its conjugate base to maintain a stable pH.

    • Dissolve the weak acid in water

    • Add the conjugate base to the solution

    • Adjust the pH as needed with a strong acid or base

    • Use a pH meter to ensure the desired pH is achieved

    • Common buffers include phosphate buffer, acetate buffer, and Tris buffer

  • Answered by AI
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Interview experience
2
Poor
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
Selected Selected

I applied via Approached by Company and was interviewed in Sep 2023. 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 Resume tips
Round 2 - Group Discussion 

Discussion due to employees in the job rules meeting with officers

Round 3 - Case Study 

Discussion about the study

Round 4 - HR 

(3 Questions)

  • Q1. Self introduction
  • Q2. Work experience
  • Q3. How much salary in these job

Interview Preparation Tips

Interview preparation tips for other job seekers - Development of work
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I applied via Naukri.com and was interviewed in Jan 2022. 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 Resume tips
Round 2 - Technical 

(3 Questions)

  • Q1. Shop floor activities in Production, From Dispensing to packing
  • Ans. 

    Shop floor activities in production involve dispensing, manufacturing, packaging, and quality control.

    • Dispensing of raw materials

    • Manufacturing of products

    • Packaging of finished goods

    • Quality control checks throughout the process

    • Cleaning and maintenance of equipment

    • Documentation of all activities

    • Training of personnel

    • Adherence to safety protocols

  • Answered by AI
  • Q2. Line clearance details, End point in granulation, critical points in RMG.
  • Q3. Compression machine parameters , and defects identify
  • Ans. 

    Compression machine parameters and defects identification

    • Compression machine parameters include force, speed, and displacement

    • Defects can be identified through visual inspection and testing

    • Common defects include cracks, voids, and delamination

    • Testing methods include ultrasonic testing and dye penetrant inspection

  • Answered by AI

Interview Preparation Tips

Topics to prepare for Medreich Executive Quality Assurance interview:
  • All IPQA activities
Interview preparation tips for other job seekers - It's best way to learn lots of knowledge and in future what will learn we determine. Thank you for this opportunity
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I applied via Referral and was interviewed in Mar 2022. There was 1 interview round.

Round 1 - One-on-one 

(1 Question)

  • Q1. Lyophilisation validation, Hvac validation,

Interview Preparation Tips

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Interview Questionnaire 

1 Question

  • Q1. Regrading in process activities
  • Ans. 

    In process activities are crucial for ensuring quality throughout the production process.

    • In process activities include inspections, testing, and monitoring of production processes.

    • These activities help identify and address quality issues before they become major problems.

    • Examples of in process activities include visual inspections, statistical process control, and product testing.

    • In process activities should be documen...

  • Answered by AI
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Interview Questionnaire 

1 Question

  • Q1. PQR preparation
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Interview experience
4
Good
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
Selected Selected

I applied via Walk-in and was interviewed before Aug 2022. There was 1 interview round.

Round 1 - Technical 

(2 Questions)

  • Q1. Experience related, personal experience,
  • Q2. Job role,teem leadership experience.

Interview Preparation Tips

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Unichem Laboratories Interview FAQs

How many rounds are there in Unichem Laboratories Quality Assurance Officer interview for experienced candidates?
Unichem Laboratories interview process for experienced candidates usually has 3 rounds. The most common rounds in the Unichem Laboratories interview process for experienced candidates are Resume Shortlist, Technical and HR.
How to prepare for Unichem Laboratories Quality Assurance Officer interview for experienced candidates?
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 Unichem Laboratories. The most common topics and skills that interviewers at Unichem Laboratories expect are Quality Assurance, IPQA, Validation, Cleaning Validation and Documentation.
What are the top questions asked in Unichem Laboratories Quality Assurance Officer interview for experienced candidates?

Some of the top questions asked at the Unichem Laboratories Quality Assurance Officer interview for experienced candidates -

  1. How to perform area clearance or equipment clearan...read more
  2. What is the role of IP...read more
  3. What is the ECR/BPR/B...read more

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Unichem Laboratories Quality Assurance Officer Salary
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