Eugia Pharma Specialities Interview Questions, Process, and Tips

Q1. Calibration of Analytical Instruments
Ans. 
Calibration of analytical instruments is essential to ensure accurate and reliable results.
• Regular calibration is necessary to maintain accuracy and precision of analytical instruments.

• Calibration involves comparing the measurements of the instrument to known standards.

• Adjustments are made to the instrument if discrepancies are found during calibration.

• Calibration records should be maintained for traceability and quali...read more
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Q2. Previous roles and responsibilities
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Handled reservations, managed bookings, provided customer service, processed payments
• Managed incoming reservations via phone, email, and online platforms

• Assisted customers with booking inquiries and changes

• Processed payments and issued refunds as needed

• Maintained accurate records of bookings and availability

• Collaborated with other departments to ensure smooth guest experience
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Q3. Troubleshooting of HPLC
Ans. 
Troubleshooting of HPLC involves identifying and resolving issues with the high-performance liquid chromatography system.
• Check for leaks in the system and tighten connections if necessary.

• Inspect the column for blockages or contamination and replace if needed.

• Calibrate the detector and ensure proper flow rate of the mobile phase.

• Troubleshoot error messages on the HPLC software by referring to the user manual.

• Consult wi...read more
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Q4. Calibration of HPLC
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Calibration of HPLC involves adjusting the settings and parameters of the equipment to ensure accurate and reliable results.
• Calibration involves checking and adjusting the flow rate, detector sensitivity, and column efficiency.

• Regular calibration helps maintain the accuracy and precision of the HPLC system.

• Calibration standards are used to verify the performance of the HPLC system.

• Calibration should be performed before...read more
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Q5. Operation of KF and Potentiometer
Ans. 
KF and Potentiometer are used in analytical chemistry for titration and pH measurements.
• KF (Karl Fischer) is used for measuring moisture content in samples.

• Potentiometer is used for measuring pH levels in solutions.

• Both instruments are essential for accurate analysis in chemistry labs.
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Q6. Why we perform standardization in KF
Ans. 
Standardization in KF is performed to ensure consistency and accuracy in measurements and results.
• Standardization helps in comparing results across different labs or studies.

• It reduces variability and improves reliability of the data.

• Standardization involves using known reference materials or methods to calibrate instruments or procedures.

• For example, in medical testing, standardization ensures that test results are ac
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Q7. Operation of Uv
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Operation of Uv involves using ultraviolet light to kill bacteria and viruses.
• Ultraviolet light is a type of electromagnetic radiation with a wavelength shorter than visible light.

• UV light can be used for disinfection purposes in water treatment, air purification, and surface sterilization.

• UV light works by damaging the genetic material of microorganisms, preventing them from reproducing.

• Examples of UV disinfection dev...read more
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Q8. If you are selected here how many days you want take leave for your marriage
Ans. 
I would like to take 5 days of leave for my marriage.
• I believe taking 5 days off would allow me to properly celebrate and enjoy my wedding.

• I will ensure all my work is up to date before taking leave.

• I can provide more details on how I plan to manage my workload during my absence if needed.
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Q9. Why you left your previous organization
Ans. 
Seeking new challenges and growth opportunities
• Desire for career advancement

• Looking for a more challenging role

• Seeking better work-life balance

• Relocation to a different city

• Company downsizing or restructuring

• Conflict with management or colleagues
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Good and very polite

Q1. Difference between DNA and RNA
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Q2. Gram's staining
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Q3. Difference between aerobic and non aerobic bacteria
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Q4. Bacterial endotoxin test
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Q5. Wather contamination test
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Q1. Aseptic practices
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Q2. QMS tools in depth
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QMS tools refer to software applications used to manage quality processes and documentation within an organization.
• QMS tools help streamline quality management processes

• Examples include ISOtrain, MasterControl, and TrackWise

• They often include features for document control, corrective actions, audits, and training management
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Q3. Media simulation
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Q4. Field alert report
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Q5. Guidelines gap assessment
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Trouble shooting, sampling

Q1. Difference between gmp and cgmp
Ans. 
GMP stands for Good Manufacturing Practices, while cGMP stands for Current Good Manufacturing Practices.
• GMP is a set of guidelines for ensuring products are consistently produced and controlled according to quality standards.

• cGMP is an updated version of GMP that includes current technologies and processes.

• cGMP is required by regulatory agencies like the FDA for pharmaceutical manufacturing.

• GMP is more general and can ...read more
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Q2. What is validation
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Validation is the process of ensuring that a product, service, or system meets the requirements and specifications set forth.
• Validation involves checking if a product meets the intended use requirements

• It ensures that the product is consistent with user needs and expectations

• Validation can include testing, inspection, and review processes

• Examples of validation include software testing to ensure it functions correctly a...read more
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Q3. What do you mean smoke study
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A smoke study is a test conducted to evaluate the airflow patterns within a cleanroom or controlled environment.
• Smoke is released into the environment to visualize the airflow patterns.

• The study helps identify areas of turbulence or dead spots where contaminants may accumulate.

• Results of the study can be used to optimize the layout of equipment and ventilation systems.

• Smoke studies are commonly used in pharmaceutical m...read more
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Q4. What is cleaning validation
Ans. 
Cleaning validation is the process of ensuring that cleaning procedures effectively remove residues from equipment used in production.
• Cleaning validation involves establishing documented evidence that cleaning procedures consistently remove residues to predetermined levels.

• It is important for ensuring product quality, preventing cross-contamination, and maintaining regulatory compliance.

• Validation typically includes sa...read more
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