Teva Pharmaceuticals Quality Executive Interview Questions and Answers

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. Based on reviews, how to review, preparation documentation
Add your answer
Q2. How to reviews of pvr& pqrs
Ans. 
Reviews of PVR and PQRS can be conducted through a systematic process involving data analysis and evaluation.
• Collect and analyze data related to PVR and PQRS

• Evaluate the performance and quality based on established criteria

• Identify areas of improvement and develop action plans

• Implement changes and monitor the impact

• Continuously review and update the process to ensure ongoing quality assurance
Answered by AI
Add your answer

Q1. Basics of analytical
Add your answer

Q1. What is NDT testing
Ans. 
NDT testing stands for Non-Destructive Testing, a method of testing materials without causing damage to them.
• NDT testing is used to detect flaws or defects in materials or products

• It is commonly used in industries such as aerospace, automotive, and construction

• Examples of NDT testing methods include ultrasonic testing, radiography, and magnetic particle testing
Answered by AI
Add your answer
Q2. What is process audit
Ans. 
Process audit is a systematic examination of a process to ensure it is meeting its objectives and requirements.
• Process audit involves reviewing the process documentation, observing the process in action, and interviewing process stakeholders.

• The goal of a process audit is to identify areas for improvement and ensure the process is efficient, effective, and compliant with standards and regulations.

• Examples of processes ...read more
Answered by AI
Add your answer
Q3. What is product audit
Ans. 
Product audit is a systematic examination of a product to ensure it meets the specified requirements and standards.
• Product audit is a quality control process that involves examining a product to ensure it meets the required specifications.

• It involves checking the product's design, manufacturing process, and final output.

• Product audit helps to identify defects, non-conformities, and areas for improvement.

• Examples of pro...read more
Answered by AI
Add your answer
Q4. Capa ,Rca,Incoming
Add your answer

Q1. Your salary expectation
Add your answer

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

Q1. Describe out of specification flow
Ans. 
Out of specification flow occurs when a product or process does not meet the required standards or specifications.
• Occurs when a product or process deviates from the specified requirements

• Can result in defects, rework, or product recalls

• Requires investigation to identify root cause and corrective actions

• May involve adjusting processes or making changes to the product design

• Can impact product quality, customer satisfacti
Answered by AI
View 1 more amswer
Q2. System suitability criteria
Ans. 
System suitability criteria are established parameters to ensure that an analytical method is suitable for its intended use.
• System suitability criteria are typically based on precision, accuracy, linearity, and robustness of the analytical method.

• These criteria are set by regulatory agencies or internal quality control standards.

• Examples of system suitability criteria include %RSD for peak area, retention time, and res...read more
Answered by AI
View 1 more amswer
Q3. Uniformity of dossage unit
Add your answer
Q4. Describe the ALCOA
Add your answer
Q5. Describe the investigation guidelines
Ans. 
Investigation guidelines outline the steps to follow when conducting an investigation.
• Clearly define the scope and objectives of the investigation

• Gather relevant evidence and information

• Interview witnesses and involved parties

• Analyze the collected data to identify root causes

• Document findings and recommendations

• Follow up on corrective actions taken
Answered by AI
View 3 more amswers

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

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
Add your answer
Q2. Line clearance details, End point in granulation, critical points in RMG.
Add your answer
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
Add your answer