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Great Pacific Exports Officer QC & QA Interview Questions and Answers

Updated 7 Jun 2023

Great Pacific Exports Officer QC & QA Interview Experiences

1 interview found

Interview experience
3
Average
Difficulty level
Moderate
Process Duration
2-4 weeks
Result
Selected Selected

I applied via Naukri.com and was interviewed before Jun 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 - Technical 

(2 Questions)

  • Q1. What is your past experinece
  • Q2. How much package do you expect

Interview Preparation Tips

Interview preparation tips for other job seekers - Be confident

Interview questions from similar companies

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

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

Round 1 - Technical 

(2 Questions)

  • Q1. What is Quality Assurance?
  • Ans. 

    Quality Assurance is a process that ensures products or services meet specified requirements and standards.

    • Quality Assurance involves creating and implementing quality control processes.

    • It focuses on preventing defects and errors rather than detecting them after production.

    • QA includes activities like planning, designing, and executing tests to ensure product quality.

    • It also involves monitoring and analyzing data to ide...

  • Answered by AI
  • Q2. Responsibilities of QA person
  • Ans. 

    The responsibilities of a QA person include ensuring the quality of products or services, identifying and reporting defects, and implementing quality control processes.

    • Developing and implementing quality assurance policies and procedures

    • Conducting tests and inspections to identify defects and ensure product or service quality

    • Documenting and reporting test results and defects

    • Collaborating with cross-functional teams to ...

  • Answered by AI
Interview experience
4
Good
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
Not Selected

I was interviewed in Nov 2024.

Round 1 - Technical 

(5 Questions)

  • Q1. What are the current Good Manufacturing Practice (cGMP) guidelines?
  • Q2. What software do you use?
  • Ans. 

    I primarily use Microsoft Excel for data analysis and reporting.

    • Microsoft Excel for data analysis

    • Quality management software for documentation and tracking

    • Statistical software for data interpretation

  • Answered by AI
  • Q3. Teell me about urself
  • Q4. Why u want chage company
  • Q5. What are ur goals
  • Ans. 

    My goal is to ensure high quality standards are met in all aspects of QA QC processes, leading to improved efficiency and customer satisfaction.

    • Implementing and maintaining quality control procedures

    • Continuous improvement of quality assurance processes

    • Training and developing team members to uphold quality standards

    • Collaborating with other departments to address quality issues

    • Achieving ISO certification for quality mana

  • Answered by AI
Interview experience
5
Excellent
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
Selected Selected

I applied via Walk-in and was interviewed before Jan 2024. There were 2 interview rounds.

Round 1 - Technical 

(2 Questions)

  • Q1. Can you describe the critical surface sampling locations for a filling line?
  • Q2. How will you prepare the surface of the glove port?
Round 2 - HR 

(1 Question)

  • Q1. Salary discussion
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

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

I applied via Campus Placement and was interviewed in Apr 2024. There were 2 interview rounds.

Round 1 - HR 

(1 Question)

  • Q1. Discuss about your project?
Round 2 - HR 

(2 Questions)

  • Q1. Discuss about subject related like disease and drugs
  • Q2. Discuss about Quality management system and Data integrity

Interview Preparation Tips

Interview preparation tips for other job seekers - So I given reply to him then he was satisfied with my answer then he selected me.
Interview experience
4
Good
Difficulty level
Moderate
Process Duration
Less than 2 weeks
Result
No response

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

Round 1 - HR 

(5 Questions)

  • Q1. HPLC principal, Gas chromatography principal, what is stationary phase Types of clinical trial Self introduction
  • Q2. What is Gas chromatography
  • Q3. What is the stationary phase inHPLC
  • Q4. Self introduction
  • Q5. How do you manage stress in job

Interview Preparation Tips

Interview preparation tips for other job seekers - Prepare for the analysis using instruments such as HPLC and gas chromatography.
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 Sep 2023. 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. Different ranges of UV visible Spectroscopy?
  • Ans. 

    UV visible spectroscopy ranges from 190 to 800 nm, with UV region being 190-400 nm and visible region being 400-800 nm.

    • UV visible spectroscopy covers a range from 190 to 800 nm.

    • The UV region ranges from 190 to 400 nm, while the visible region ranges from 400 to 800 nm.

    • UV visible spectroscopy is commonly used in analytical chemistry to determine the presence of certain compounds based on their absorption of UV or visibl

  • Answered by AI
  • Q2. What are the different dosage forms ?
  • Q3. Why should we hire you for a role as a pharma QA?
  • Q4. Why do you want to work with us?

I applied via Walk-in and was interviewed in May 2022. There were 2 interview rounds.

Round 1 - Technical 

(2 Questions)

  • Q1. Based on CV, and based on experience in the Work
  • Q2. Real time work experience is enough.
Round 2 - HR 

(1 Question)

  • Q1. Why do you change job.

Interview Preparation Tips

Interview preparation tips for other job seekers - Be prepared. There is no complicate. They will more negotiate in salary.
Interview experience
4
Good
Difficulty level
Moderate
Process Duration
More than 8 weeks
Result
Selected Selected

I applied via Naukri.com and was interviewed before Oct 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 tips
Round 2 - One-on-one 

(2 Questions)

  • Q1. TGA Guidelines Sterilization QMS
  • Q2. All mentioned in CV

Interview Preparation Tips

Interview preparation tips for other job seekers - Be prepared as per job role & JD

Great Pacific Exports Interview FAQs

How many rounds are there in Great Pacific Exports Officer QC & QA interview?
Great Pacific Exports interview process usually has 2 rounds. The most common rounds in the Great Pacific Exports interview process are Resume Shortlist and Technical.

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Great Pacific Exports Officer QC & QA Interview Process

based on 1 interview

Interview experience

3
  
Average
View more

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