Senior Quality Executive

40+ Senior Quality Executive Interview Questions and Answers

Updated 28 Oct 2024
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Q1. Your qualification is in different area and work experience/ career is in different area, Why?

Ans.

My education provided me with a strong foundation in quality management principles, which I have applied in my work experience.

  • My education in quality management principles has given me a strong foundation for this role

  • I have applied these principles in my previous work experience

  • My diverse background allows me to bring a unique perspective to the role

  • I am confident that my skills and experience make me a strong candidate for this position

Q2. What is the process to identify the issue and how to resolve complete process

Ans.

The process to identify and resolve issues involves root cause analysis, corrective actions, and preventive measures.

  • Conduct a root cause analysis to determine the underlying issue

  • Implement corrective actions to address the identified problem

  • Develop preventive measures to avoid similar issues in the future

  • Monitor the effectiveness of the solutions implemented

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Q3. What is Experince ? What is Bet ,? Total pharma experince )? Validation product Salary acceptation ? Last experince? Things that learnt ?

Ans.

Experience refers to the knowledge, skills, and understanding gained through practical involvement in a particular field or activity.

  • Experience is acquired through hands-on involvement in a specific field or activity.

  • It includes knowledge, skills, and understanding gained over time.

  • Experience can be gained through work, education, training, or personal involvement.

  • It helps individuals develop expertise and proficiency in their chosen field.

  • Experience is valuable for problem-s...read more

Q4. What do you know the raw material and FG product testing process.

Ans.

The raw material and FG product testing process involves thorough analysis to ensure quality standards are met.

  • Raw material testing involves checking for purity, composition, and potential contaminants.

  • Finished goods testing includes physical, chemical, and microbiological analysis.

  • Testing methods may include chromatography, spectroscopy, and microbial testing.

  • Quality control measures are implemented to ensure compliance with regulations and standards.

  • Results are documented a...read more

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Q5. How to handle large no. of centres quality part?

Ans.

Develop a systematic approach to monitor and evaluate quality across all centres.

  • Establish clear quality standards and guidelines for all centres.

  • Develop a comprehensive quality assurance program.

  • Conduct regular audits and inspections to ensure compliance with standards.

  • Provide training and support to centre staff to improve quality.

  • Implement a system for collecting and analyzing data on quality performance.

  • Use technology to streamline quality monitoring and reporting.

  • Establi...read more

Q6. How to implement Lean Manufacturing in line

Ans.

Implementing Lean Manufacturing involves identifying waste, streamlining processes, and continuous improvement.

  • Identify and eliminate waste in the production process

  • Streamline processes to improve efficiency and reduce lead times

  • Implement visual management tools such as Kanban boards to track progress

  • Encourage employee involvement and empowerment to drive continuous improvement

  • Utilize tools like 5S to organize the workplace and standardize processes

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Q7. What you know about Quality assurance?

Ans.

Quality assurance is a process of ensuring that products or services meet the desired level of quality.

  • It involves creating and implementing quality standards and procedures.

  • It includes monitoring and evaluating the quality of products or services.

  • It aims to identify and correct any defects or issues in the production process.

  • It helps to improve customer satisfaction and loyalty.

  • Examples include conducting quality audits, implementing quality control measures, and providing t...read more

Q8. What is DDU-GKY SOP for quality part?

Ans.

DDU-GKY SOP for quality part is a set of guidelines and procedures to ensure high standards of quality in the program.

  • DDU-GKY SOP for quality part outlines the steps to be followed to maintain quality in the program

  • It includes guidelines for monitoring and evaluation of training programs

  • It defines the criteria for assessing the quality of training providers

  • It specifies the process for conducting quality audits and inspections

  • It provides a framework for addressing quality issu...read more

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Q9. Different between method validation and method development

Ans.

Method validation is confirming that a method is suitable for its intended use, while method development is creating a new method.

  • Method validation ensures that a method is reliable, accurate, and consistent for its intended use.

  • Method development involves creating a new method from scratch or modifying an existing one to improve its performance.

  • Validation is a necessary step before a method can be used for routine testing, while development is done to improve the method's pe...read more

Q10. How to calculate Out of trends

Ans.

Out of trends can be calculated by analyzing data points and identifying deviations from expected trends.

  • Collect data points over a period of time

  • Plot the data points on a graph

  • Identify the expected trend based on historical data

  • Analyze the data points to identify any deviations from the expected trend

  • Calculate the percentage of data points that fall outside the expected trend

  • Investigate the reasons for the deviations and take corrective actions

Q11. What do you understand by test plan?

Ans.

A test plan is a document outlining the approach, resources, schedule, and scope of testing activities.

  • Test plan defines the testing activities to be conducted, such as test objectives, test strategies, and test deliverables.

  • It includes details on test environment setup, test cases to be executed, and the criteria for entry and exit from testing.

  • Test plan also outlines the roles and responsibilities of team members involved in testing.

  • It serves as a roadmap for the testing pr...read more

Q12. Hplc principle and it's comparison with other technology

Ans.

HPLC is a chromatography technique used to separate, identify, and quantify components in a mixture based on their interactions with a stationary phase and a mobile phase.

  • HPLC stands for High Performance Liquid Chromatography.

  • It is commonly used in pharmaceutical, environmental, and food industries for quality control and research purposes.

  • HPLC is more sensitive and provides higher resolution compared to other chromatography techniques like TLC (Thin Layer Chromatography) and...read more

Q13. Lean Six Sigma Black Belt Project describe

Ans.

A Lean Six Sigma Black Belt project involves using data-driven methods to improve processes and reduce waste.

  • Identify a problem or inefficiency in a process

  • Collect and analyze data to understand the root cause

  • Implement solutions to improve the process

  • Measure the impact of the changes to ensure improvement

  • Certification as a Lean Six Sigma Black Belt is required to lead these projects

Q14. Tell me about expected package?

Ans.

The expected package for the Senior Quality Executive position will depend on factors such as experience, qualifications, and industry standards.

  • The expected package will be competitive and in line with industry standards.

  • It will be based on the candidate's qualifications, experience, and skills.

  • Additional benefits such as health insurance, retirement plans, and performance bonuses may also be included.

  • The package may vary depending on the company's size, location, and financ...read more

Q15. how do INLINE , MID , FINAL INSPECTION

Ans.

INLINE, MID, and FINAL INSPECTION are three stages of quality control in manufacturing.

  • INLINE INSPECTION is done during the manufacturing process to ensure that each step is completed correctly.

  • MID INSPECTION is done after a certain percentage of the manufacturing process is completed to catch any issues early on.

  • FINAL INSPECTION is done at the end of the manufacturing process to ensure that the final product meets all quality standards.

  • These inspections help to identify and ...read more

Q16. Types of compressor and process

Ans.

Compressors are categorized into positive displacement and dynamic types. Processes include compression, cooling, and transportation.

  • Types of compressors: positive displacement (reciprocating, rotary screw, rotary vane) and dynamic (centrifugal, axial flow)

  • Processes: compression (increasing pressure of gas), cooling (removing heat from gas), transportation (moving gas from one location to another)

Q17. What Product knowledge ?

Ans.

Product knowledge refers to the understanding and familiarity with the features, functions, and benefits of a particular product or range of products.

  • Understanding the product's specifications and technical details

  • Knowing the product's target market and customer needs

  • Being aware of the product's competitive advantages and unique selling points

  • Understanding the product's lifecycle and any potential issues or limitations

  • Being familiar with the product's pricing, packaging, and ...read more

Q18. What is the p2p cycle ?

Ans.

The p2p cycle refers to the procure-to-pay cycle, which is the process of obtaining and paying for goods and services.

  • The cycle starts with the need for goods or services, followed by the selection of suppliers and negotiation of terms.

  • Purchase orders are then created, goods or services are received, and invoices are processed for payment.

  • The final step involves reconciling invoices with purchase orders and receiving reports to ensure accuracy and completion of the transactio...read more

Q19. What is conflict management

Ans.

Conflict management is the process of handling disputes or disagreements in a constructive way to reach a resolution.

  • Identifying the source of conflict

  • Listening to all parties involved

  • Finding common ground and understanding each other's perspectives

  • Collaboratively working towards a solution

  • Implementing strategies to prevent future conflicts

Q20. how to control Quality

Ans.

Quality can be controlled through a systematic approach that involves planning, monitoring, and continuous improvement.

  • Establish clear quality standards and objectives

  • Implement quality control measures at every stage of the production process

  • Regularly monitor and measure quality performance

  • Identify and address quality issues promptly

  • Continuously improve quality through feedback and analysis

  • Train and educate employees on quality control and improvement

  • Use technology and automa...read more

Q21. Work ability in fixed work time

Ans.

Work ability in fixed work time refers to the ability of an individual to effectively perform their job responsibilities within a set schedule.

  • Efficient time management skills are essential for maximizing work ability in fixed work time.

  • Setting clear priorities and deadlines can help improve work ability within a fixed schedule.

  • Regular breaks and proper rest are important for maintaining work ability throughout the work day.

  • Utilizing tools and technology to streamline tasks c...read more

Q22. Lean Six Sigma project describe

Ans.

A Lean Six Sigma project is a process improvement initiative that aims to reduce waste and improve efficiency by using data-driven methodologies.

  • Identify the problem or opportunity for improvement

  • Define the project scope and goals

  • Measure current process performance using data

  • Analyze the data to identify root causes of issues

  • Implement solutions to address the root causes

  • Control and monitor the improved process to sustain the gains

  • Examples: reducing defects in manufacturing, st...read more

Q23. How know about weblink ?

Ans.

Weblink is a hyperlink or URL that directs to a webpage or website.

  • A weblink is a clickable link that takes you to a webpage or website.

  • Weblinks can be found in emails, documents, social media posts, and websites.

  • Weblinks can be shortened using services like bit.ly or TinyURL.

  • Weblinks can be used for various purposes such as sharing information, promoting products, or directing traffic to a website.

Q24. PHE's catalogue type and troubleshooting

Ans.

PHE's catalogue type and troubleshooting

  • PHE stands for Public Health England

  • Catalogue type refers to the classification and organization of products or services offered by PHE

  • Troubleshooting involves identifying and resolving issues or problems with PHE's catalogue

Q25. How to manage work?

Ans.

Managing work involves setting priorities, delegating tasks, staying organized, and communicating effectively.

  • Set clear goals and priorities

  • Create a schedule and stick to it

  • Delegate tasks to team members based on their strengths

  • Use tools like project management software to stay organized

  • Communicate regularly with team members to ensure everyone is on the same page

Q26. What is accuracy?

Ans.

Accuracy refers to the degree of closeness between a measured value and the true value of a quantity being measured.

  • Accuracy is a measure of how correct a result is compared to the true value.

  • It is often expressed as a percentage or a fraction.

  • For example, if a scale is accurate to within 0.1 grams, it means that the measured weight is within 0.1 grams of the actual weight.

Q27. What is calibration?

Ans.

Calibration is the process of comparing measurements of an instrument or device with a known standard to ensure accuracy.

  • Calibration involves adjusting the instrument or device to align with the standard.

  • It is essential for maintaining accuracy and reliability in measurements.

  • Examples include calibrating thermometers, scales, and pressure gauges.

  • Calibration certificates are often provided as proof of accuracy.

Q28. What is uncertainty?

Ans.

Uncertainty refers to the lack of knowledge or information about a situation, leading to unpredictability or doubt.

  • Uncertainty can arise from incomplete information or conflicting data.

  • It can lead to indecision or hesitation in making decisions.

  • Uncertainty is a common factor in risk assessment and management.

  • Examples include uncertain market conditions, ambiguous test results, or unpredictable outcomes.

Q29. SOP of food products preparation

Ans.

SOP for food product preparation involves a set of guidelines to ensure consistency and safety in the production process.

  • SOP should include detailed instructions for each step of the process

  • It should cover aspects such as hygiene, equipment usage, and ingredient handling

  • Regular training and monitoring should be conducted to ensure adherence to SOP

  • Examples of SOPs include HACCP and GMP

  • SOPs should be regularly reviewed and updated to reflect changes in regulations or best pract...read more

Q30. Work feasibility at remote locations

Ans.

Remote work feasibility depends on infrastructure, communication tools, and employee discipline.

  • Ensure reliable internet connection is available at remote locations.

  • Provide necessary communication tools like video conferencing software.

  • Establish clear expectations and guidelines for remote work.

  • Monitor productivity and performance regularly.

  • Encourage regular communication and collaboration among remote team members.

Q31. Kind of hplc detector

Ans.

The kind of HPLC detector used in chromatography analysis.

  • Common types include UV-Vis, fluorescence, refractive index, and conductivity detectors

  • Choice of detector depends on the analyte being measured and the sensitivity required

  • UV-Vis detectors are widely used for general purpose analysis

  • Fluorescence detectors are more sensitive and selective for certain compounds

Q32. What do you mean spc

Ans.

SPC stands for Statistical Process Control.

  • SPC is a method used to monitor and control processes to ensure they are operating within acceptable limits.

  • It involves collecting and analyzing data to identify and reduce variation in a process.

  • SPC uses statistical techniques such as control charts to visualize and interpret data.

  • It helps in identifying and addressing process issues, improving quality, and reducing defects.

  • Example: SPC can be used in manufacturing to monitor the di...read more

Q33. Ich full form in the form

Ans.

The full form of 'ICH' is 'International Conference on Harmonisation'.

  • ICH is a global initiative to standardize regulations for pharmaceuticals.

  • It aims to ensure the safety, quality, and efficacy of pharmaceutical products.

  • Examples of ICH guidelines include Q1A (Stability Testing) and Q2 (Validation of Analytical Procedures).

Q34. Problem solving techniques

Ans.

Problem solving techniques involve identifying the root cause, brainstorming solutions, evaluating options, and implementing the best solution.

  • Identify the problem and its root cause

  • Brainstorm potential solutions

  • Evaluate each solution based on feasibility and impact

  • Select the best solution and create an action plan

  • Implement the solution and monitor its effectiveness

Q35. Classification of deviations

Ans.

Deviations are classified based on their impact on product quality and regulatory compliance.

  • Deviations are typically classified as critical, major, or minor based on their severity.

  • Critical deviations have a significant impact on product quality and regulatory compliance.

  • Major deviations have a moderate impact on product quality and regulatory compliance.

  • Minor deviations have a minimal impact on product quality and regulatory compliance.

  • Examples of critical deviations includ...read more

Q36. Examples of deviations

Ans.

Deviations are instances where a process or product does not meet specified requirements or standards.

  • Incorrect labeling on a product

  • Equipment malfunction during production

  • Failure to follow standard operating procedures

  • Out-of-specification test results

  • Non-conformance to regulatory requirements

Q37. Gdp full form elaborate

Ans.

GDP stands for Gross Domestic Product, which is a measure of a country's economic performance.

  • GDP is the total value of all goods and services produced within a country's borders in a specific time period.

  • It is used to gauge the economic health and growth of a country.

  • GDP can be calculated using three different approaches: production, income, and expenditure.

  • For example, if a country's GDP is $1 trillion, it means that the country produced $1 trillion worth of goods and servi...read more

Q38. Review of Analytical data

Ans.

Reviewing analytical data is crucial for ensuring quality and identifying any issues.

  • Analytical data should be reviewed regularly to ensure accuracy and consistency.

  • Any discrepancies or outliers should be investigated and addressed.

  • Reviewing analytical data can help identify trends and areas for improvement.

  • Examples of analytical data include test results, product specifications, and process parameters.

Q39. Explain examples

Ans.

Examples are specific instances or cases that illustrate a concept or idea.

  • Examples help to clarify complex concepts and make them easier to understand.

  • They provide real-world context and practical applications for theoretical knowledge.

  • Using examples can enhance learning and retention of information.

  • For instance, in quality management, examples of successful quality improvement projects can demonstrate best practices to follow.

Q40. Gmp full form elaborate

Ans.

GMP stands for Good Manufacturing Practice, which is a set of guidelines and regulations ensuring the quality and safety of pharmaceutical products.

  • GMP is a system for ensuring that products are consistently produced and controlled according to quality standards.

  • It covers all aspects of production from the starting materials, premises, and equipment to the training and personal hygiene of staff.

  • Examples of GMP requirements include proper documentation, validation of processes...read more

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