Granules India Quality Assurance Officer Interview Questions and Answers

Q1. Job responsibilities
Add your answer
Q2. Quality assurance questions
Add your answer

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
Answered by AI
Add your answer
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
Answered by AI
Add your answer
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
Answered by AI
Add your answer
Q4. Asking about APQR
Add your answer
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
Answered by AI
Add your answer

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
Answered by AI
Add your answer
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
Answered by AI
Add your answer
Q3. USP chapters of Microbial tesing of API and water
Add your answer
Q4. Growth Pramotion tests
Add your answer
Q5. Horizontal Autoclave validation
Add your answer
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
Answered by AI
Add your answer

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

Q1. Discuss about your project?
Add your answer

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

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...read more
Answered by AI
Add your answer
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...read more
Answered by AI
Add your answer
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...read more
Answered by AI
Add your answer
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
Add your answer

Q1. Salary discussion and company policies
Add your answer

Q1. Your salary expectation
Add your answer

Q1. Questions about your profile mentioned in your resume
Add your answer

Q1. Selection of die ,Aql,alc,ccp,cqa, stratified sampling,data integrity,GMP,GDP etc
Add your answer
Q2. Stratified sampling
Add your answer

Q1. Self introduction
Add your answer
Q2. Personal profile previous experience etc
Add your answer

Q1. Experience related, personal experience,
Add your answer
Q2. Job role,teem leadership experience.
Add your answer

Q1. Different between QA and QC
Ans. 
QA focuses on preventing defects in the process, while QC focuses on identifying defects in the product.
• QA is process oriented, focusing on preventing defects by establishing processes and standards.

• QC is product oriented, focusing on identifying defects through testing and inspection.

• QA involves activities like process audits, training, and documentation.

• QC involves activities like product testing, inspections, and sa...read more
Answered by AI
Add your answer
Q2. Types of defect
Ans. 
Types of defects include functional, performance, cosmetic, and compatibility issues.
• Functional defects affect the core functionality of the product or system.

• Performance defects impact the speed, response time, or resource usage.

• Cosmetic defects are related to the appearance or aesthetics of the product.

• Compatibility defects arise when the product does not work well with other systems or devices.
Answered by AI
Add your answer

Standard of coding and defect of coding