Adept Pharma And Bioscience Senior Executive Interview Questions and Answers

Q1. What is common mutation in CFTR gene
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Q1. What are product and process related impurities?
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Q2. What are Method development parameters as per ICH
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Method development parameters as per ICH
• ICH guidelines provide recommendations for method development in the pharmaceutical industry

• Parameters include specificity, linearity, range, accuracy, precision, robustness, and system suitability

• Specificity ensures that the method measures only the analyte of interest

• Linearity determines the relationship between analyte concentration and response

• Range defines the concentration ...read more
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Q1. CSV Validation activities, It sop procedure, data backup, test script writing and review,
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Q2. What is CSV and how can you prepare the validation deliverables?
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CSV stands for Comma Separated Values and is a file format used to store data in a tabular form.
• CSV files can be created using spreadsheet software like Microsoft Excel or Google Sheets.

• Validation deliverables for CSV files include verifying the accuracy of data, ensuring proper formatting, and checking for any errors or inconsistencies.

• Validation can be done manually or through automated tools like scripts or software...read more
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Q1. Vaccine manufacturing
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Q2. Yourself about and planning batch
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Q1. My profile and my previous company profile details asking me.
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Q2. Job related and challenging work related growth in and development related asking me
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Q1. Qc microbiology specialization
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Q1. What is thee fill volume formula ?
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The fill volume formula calculates the volume of liquid or gas that can be held in a container.
• The fill volume formula is typically calculated by multiplying the area of the base of the container by its height.

• For example, the fill volume of a cylindrical tank can be calculated using the formula V = πr^2h, where r is the radius of the base and h is the height of the tank.

• Different shapes of containers will have differe...read more
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Q2. Difference between dynamic and static pass box ?
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Dynamic pass box allows for continuous transfer of materials while static pass box requires manual transfer.
• Dynamic pass box has a conveyor belt for continuous transfer of materials.

• Static pass box requires manual transfer of materials.

• Dynamic pass box is more efficient for high volume transfer.

• Static pass box is suitable for low volume transfer or when contamination risk is high.

• Examples: Pharmaceutical industry uses ...read more
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Q3. How we classified Clean Room Areas ?
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Clean room areas are classified based on the level of cleanliness required for the specific activities performed within them.
• Clean room areas are classified using ISO standards, with Class 1 being the cleanest and Class 9 being the least clean.

• The classification is based on the maximum allowable concentration of particles per cubic meter of air.

• Examples of clean room areas include semiconductor manufacturing facilities...read more
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Q4. What is BIO-SAFETY CABINET ?
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Genetic variants interpretation significance in diseases.

Q1. Details discussion of genetic variants significance in the assessment risk development and their role in development of genetic disorders.
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Q2. What is Mendelian disorders
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Q3. Sickle cell anemia, Cruzfelt Jacob disease, Lung fibrosis
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Q4. What is frame shift mutation, missense mutation
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Q5. What are ACMG and AMP guidelines
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