Celon Laboratories Senior Executive QA Interview Questions and Answers

Q1. About ur self with current job profile
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Q2. Currently handling critical category change control in ur current job
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Yes, I am currently responsible for handling critical category change control in my current job.
• I am responsible for reviewing and approving change controls for critical categories such as manufacturing processes, equipment, and raw materials.

• I ensure that all changes are properly documented, assessed for impact, and implemented in a timely manner to minimize any potential risks.

• I work closely with cross-functional tea...read more
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Q3. What's Alcoa++ principal
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Alcoa++ principal is a quality management principle focusing on continuous improvement and prevention of defects.
• Continuous improvement is achieved through ongoing monitoring and evaluation of processes.

• Prevention of defects involves identifying root causes and implementing corrective actions.

• Alcoa++ is a variation of the original Alcoa principle, which stands for 'Accident Loss Control Over All'.
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Q4. Current schedule M in plant and R&D
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Q5. What's is process to prepare Pv with reference gaidlince
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Preparing Process Validation with reference to guidelines involves following a structured approach.
• Understand the guidelines provided by regulatory authorities or industry standards

• Identify the critical process parameters and validation criteria

• Develop a validation protocol outlining the validation approach, acceptance criteria, and testing methods

• Execute the validation protocol by conducting tests, collecting data, an...read more
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Q6. Q14 current updates with briefly details
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Current updates in quality assurance include implementation of new software tools, training on updated regulations, and continuous improvement initiatives.
• Implementation of new software tools to streamline quality assurance processes

• Training on updated regulations to ensure compliance with industry standards

• Continuous improvement initiatives to enhance quality control measures

• Integration of automation and AI technologi
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Q1. Senior person taken interview
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Q2. What's is rol in current company
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My role in the current company is to ensure quality assurance processes are followed to maintain high standards of products and services.
• Leading a team of QA professionals to conduct testing and inspections

• Developing and implementing quality assurance policies and procedures

• Collaborating with other departments to address quality issues and improve processes

• Analyzing data and reports to identify areas for improvement

• Tra...read more
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Q3. Stability in current company
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I have been with my current company for 5 years and have consistently demonstrated stability through my dedication and commitment to my role.
• I have been with my current company for 5 years

• I have received positive feedback from my supervisors on my stability and reliability

• I have consistently met or exceeded performance expectations

• I have not had any significant gaps in my employment history
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Q4. Currently handling total team.
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Q5. QMs tools and risk assessment briefly details
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Q6. Cleaning validation calculation and Worst condition selection criteria
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Q1. Salary details with all previous company documents
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Q2. Notes periods for previous company
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Notes periods for previous company
• Worked at XYZ Company from Jan 2015 to Mar 2018

• Promoted to Senior QA Analyst in May 2016

• Took a 3-month sabbatical in 2017 for personal reasons
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Test related of my subject knowledge

Q1. Quality head ask questions about pharmacy act and schedules in pharmacy.
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Q1. General introduction
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Q1. Related job profile and experience related your own work
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Q2. What is your job profile current and how u can handle your work and previous company work experience
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Q3. What is validation and types of validation
Ans. 
Validation is the process of ensuring that a system or product meets the specified requirements and standards.
• Types of validation include: functional validation, performance validation, security validation, usability validation, and compliance validation.

• Functional validation ensures that the system or product meets the functional requirements.

• Performance validation ensures that the system or product meets the performa...read more
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Q1. What is gmp in pharma
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Q2. What is ALCOA principle
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ALCOA principle is a guideline for ensuring data integrity in regulated industries, emphasizing data should be attributable, legible, contemporaneous, original, and accurate.
• Attributable - Data should be traceable to its source.

• Legible - Data should be clear and easy to read.

• Contemporaneous - Data should be recorded at the time of observation.

• Original - Data should be the first recording of the information.

• Accurate - D...read more
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Q1. Balance calibration record
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Q2. Current profile and work
Ans. Give answer as per your current profile in confident way
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Q3. Balance calibration how it is done
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Balance calibration is done by comparing the readings of the balance with known weights.
• Balance calibration involves comparing the readings of the balance with known weights.

• Known weights are placed on the balance and the readings are recorded.

• The readings are then compared to the expected values to determine if the balance is accurate.

• Adjustments can be made to the balance if necessary to ensure accurate readings.

• Regu...read more
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Q1. Are you able to relocate
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Q2. This has to be asked
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Q1. Previous KRA and job role
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Q1. Previous experience
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Related job roles and work culture