USV Manager Quality Assurance Interview Questions and Answers

Q1. What is Ppap and should do ppap
Ans. 
PPAP stands for Production Part Approval Process. It is a standardized process in the automotive industry to ensure suppliers meet quality standards.
• PPAP is a set of guidelines developed by the Automotive Industry Action Group (AIAG) to establish a common understanding between suppliers and manufacturers.

• It involves submitting documentation such as design records, process flow diagrams, control plans, and measurement s...read more
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Q2. How many types of compressor
Ans. 
There are two main types of compressors: positive displacement compressors and dynamic compressors.
• Positive displacement compressors include reciprocating, rotary screw, and rotary vane compressors.

• Dynamic compressors include centrifugal and axial compressors.

• Each type of compressor has its own advantages and disadvantages based on the application and requirements.
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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...read more
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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...read more
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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...read more
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Q4. Asking about APQR
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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...read more
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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...read more
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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...read more
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Q3. USP chapters of Microbial tesing of API and water
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Q4. Growth Pramotion tests
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Q5. Horizontal Autoclave validation
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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...read more
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Q1. Tell me about your self
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Q2. Are you willing to shift Vizag
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Q3. Salary discussion
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Q1. Food safety related questions
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Q2. Related to process like OPRP,PRP,HACCP,5S
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Quality assurance analysis

Q1. My bio data any my sesum
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Q2. My introduction my experience
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Q1. 7q 4m 5s ppm iqc in meson my resume
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Maend test

Group discussion

Q1. 7 Qc tool ,4m ,3R,5s,
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Q1. Change control , deviation , market complaints
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Q1. Instrument and food safety related questions
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Ask about basic maths