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20+ Vignesh Hitechcity 2 Society Interview Questions and Answers

Updated 13 Aug 2024

Q1. Necessary checking procedure of Glass lined reactor.

Ans.

The necessary checking procedure of a glass lined reactor involves visual inspection, pressure testing, and checking for any signs of corrosion or damage.

  • Perform a visual inspection of the glass lining to check for any cracks, chips, or signs of wear.

  • Conduct a pressure test to ensure the reactor can withstand the required operating pressure.

  • Check for any signs of corrosion on the glass lining, especially in areas exposed to corrosive substances.

  • Inspect the reactor's accessori...read more

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Q2. What is difference between calibration and validation

Ans.

Calibration is the process of adjusting an instrument to ensure accurate measurements, while validation is the process of ensuring that a method or process produces accurate and reliable results.

  • Calibration involves adjusting an instrument to ensure that it provides accurate measurements.

  • Validation involves ensuring that a method or process produces accurate and reliable results.

  • Calibration is a process that is performed on instruments, while validation is a process that is p...read more

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Q3. What is assay by HPLC and ehy perform?

Ans.

Assay by HPLC is a technique used to separate, identify, and quantify components in a sample.

  • HPLC stands for High-Performance Liquid Chromatography.

  • It is commonly used in pharmaceutical and chemical industries for quality control purposes.

  • Assay by HPLC involves injecting a sample into a high-pressure liquid chromatography system, where the components are separated based on their interactions with the stationary phase.

  • The separated components are then detected and quantified u...read more

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Q4. How prepared 1.0 N NaoH solution?

Ans.

To prepare a 1.0 N NaOH solution, dissolve 40.0 g of NaOH in enough water to make 1 liter of solution.

  • To prepare a 1.0 N NaOH solution, you need to know the molar mass of NaOH (40.0 g/mol).

  • Calculate the number of moles of NaOH required using the formula: moles = N x volume (in liters).

  • For a 1.0 N solution, the number of moles of NaOH is equal to the desired concentration (1.0 mol/L).

  • Weigh 40.0 g of NaOH using a balance.

  • Dissolve the weighed NaOH in a small amount of water to m...read more

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Q5. What is molecular weight of HNO3?

Ans.

The molecular weight of HNO3 is 63.01 g/mol.

  • The molecular weight of a compound is the sum of the atomic weights of all the atoms in its chemical formula.

  • For HNO3, the atomic weight of hydrogen (H) is 1.01 g/mol, nitrogen (N) is 14.01 g/mol, and oxygen (O) is 16.00 g/mol.

  • Multiplying the atomic weights by the number of atoms in the formula (1 hydrogen, 1 nitrogen, and 3 oxygen) and summing them gives the molecular weight of HNO3 as 63.01 g/mol.

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Q6. What is molecular weight of ACETIC ACID?

Ans.

The molecular weight of acetic acid is 60.052 g/mol.

  • The molecular weight of a compound is the sum of the atomic weights of all the atoms in its chemical formula.

  • The chemical formula of acetic acid is CH3COOH.

  • The atomic weights of carbon (C), hydrogen (H), and oxygen (O) are 12.01 g/mol, 1.008 g/mol, and 16.00 g/mol respectively.

  • Calculating the molecular weight of acetic acid: (12.01 * 2) + (1.008 * 4) + 16.00 + 1.008 = 60.052 g/mol.

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Q7. How calibration of karl fisher?

Ans.

Calibration of Karl Fischer is a process to ensure accuracy and reliability of the moisture determination method.

  • Calibration involves verifying the performance of the Karl Fischer titration system.

  • It includes checking the accuracy of the reagents, electrodes, and the instrument itself.

  • Calibration is typically done using standard solutions with known moisture content.

  • The instrument readings are compared to the expected values to determine any deviations.

  • Adjustments are made to...read more

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Q8. What is R. S in HPLC?

Ans.

R. S in HPLC stands for Relative Standard Deviation.

  • R. S is a measure of the precision or reproducibility of an HPLC method.

  • It is calculated by dividing the standard deviation of peak areas by the average peak area and multiplying by 100.

  • R. S is expressed as a percentage and indicates the variability of peak areas in replicate injections.

  • A lower R. S value indicates higher precision and better method performance.

  • For example, if the R. S value is 2%, it means that the peak are...read more

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Q9. Types of steam traps.Working of steam traps.

Ans.

Steam traps are devices used to discharge condensate and non-condensable gases from steam systems.

  • There are three main types of steam traps: mechanical, thermostatic, and thermodynamic.

  • Mechanical steam traps use a float to open and close a valve.

  • Thermostatic steam traps use a temperature-sensitive element to open and close a valve.

  • Thermodynamic steam traps use the difference in pressure between steam and condensate to operate a valve.

  • Steam traps prevent steam from escaping an...read more

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Q10. Blend unifomity calculation and how to select die.

Ans.

Blend uniformity calculation and die selection for QA/QC Manager role.

  • Blend uniformity calculation involves determining the homogeneity of a mixture.

  • It is important to select the appropriate die for the blend to ensure consistent tablet weight and hardness.

  • Factors to consider when selecting a die include tablet size, shape, and desired release profile.

  • Die selection should also take into account the properties of the active ingredient and excipients used in the blend.

  • Regular t...read more

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Q11. How calibration of HPLC?

Ans.

Calibration of HPLC involves verifying the accuracy and precision of the instrument by comparing the results obtained with known standards.

  • Calibration of HPLC is essential to ensure accurate and reliable results.

  • It involves preparing a series of standard solutions with known concentrations of analytes.

  • These standard solutions are then injected into the HPLC system and the peak areas or heights are measured.

  • The obtained data is used to create a calibration curve, which relates...read more

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Q12. Types of vaccum systems with working.

Ans.

There are two types of vacuum systems: liquid ring and dry vacuum systems.

  • Liquid ring vacuum systems use a liquid as a sealant to create a vacuum.

  • Dry vacuum systems use oil-free pumps to create a vacuum.

  • Examples of liquid ring vacuum systems include steam jet ejectors and water ring vacuum pumps.

  • Examples of dry vacuum systems include scroll pumps and turbo molecular pumps.

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Q13. Trouble shooting of Flush bottom valve.

Ans.

Flush bottom valves are used to drain liquids from tanks. Troubleshooting involves identifying and fixing issues with the valve.

  • Check for leaks or blockages in the valve

  • Inspect the valve for damage or wear and tear

  • Ensure that the valve is properly installed and tightened

  • Verify that the valve is compatible with the liquid being drained

  • Consult manufacturer's instructions or seek expert advice if necessary

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Q14. Requirement of U-loop in steam lines.

Ans.

U-loop is required in steam lines to prevent thermal expansion and contraction.

  • U-loop is a type of expansion joint used in steam lines.

  • It is used to absorb the thermal expansion and contraction of the pipe.

  • It prevents the pipe from buckling or breaking due to thermal stress.

  • U-loop is typically installed in vertical steam lines.

  • It is also used in horizontal steam lines where there is limited space for expansion.

  • U-loop is designed to accommodate both axial and lateral movement ...read more

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Q15. How did you calculate the F0 value.

Ans.

The F0 value is calculated by...

  • F0 value is calculated using the formula...

  • To calculate the F0 value, you need to...

  • The F0 value can be determined by...

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Q16. How to maintain aseptic condition.

Ans.

Maintaining aseptic conditions involves implementing strict hygiene practices and using sterile equipment to prevent contamination.

  • Follow proper hand hygiene protocols, including washing hands thoroughly with soap and water or using alcohol-based hand sanitizers.

  • Wear appropriate personal protective equipment (PPE) such as gloves, masks, and gowns.

  • Ensure the cleanliness and sterility of the production area by regularly cleaning and disinfecting surfaces and equipment.

  • Use steri...read more

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Q17. What is resolution?

Ans.

Resolution refers to the ability to distinguish between two separate points or objects in an image or display.

  • Resolution is a measure of the level of detail in an image or display.

  • It is typically measured in terms of pixels or dots per inch (DPI).

  • Higher resolution means more pixels or dots, resulting in a clearer and sharper image.

  • Resolution is important in various fields such as photography, video production, and display technology.

  • For example, a high-resolution camera can c...read more

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Q18. What is the expected CTC do you want

Ans.

I am looking for a competitive CTC based on my experience, skills, and the industry standards.

  • I am seeking a CTC that reflects my qualifications and contributions to the organization

  • I am open to negotiation based on the overall compensation package offered

  • I have researched industry standards and salary benchmarks to determine a reasonable CTC expectation

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Q19. How to do Tunnel validation

Ans.

Tunnel validation involves checking the integrity and functionality of tunnels for various purposes.

  • Check for proper ventilation and lighting inside the tunnel

  • Inspect for any signs of water leakage or structural damage

  • Test communication systems to ensure connectivity throughout the tunnel

  • Verify emergency exits and evacuation procedures

  • Conduct regular maintenance and monitoring for safety

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Q20. How to vial washing validation

Ans.

Vial washing validation involves ensuring the cleanliness and sterility of vials used in pharmaceutical production.

  • Develop a validation protocol outlining the procedures and acceptance criteria for vial washing

  • Perform a risk assessment to identify critical control points in the vial washing process

  • Conduct studies to validate the effectiveness of the vial washing equipment and process

  • Use appropriate analytical methods to test for residues and microbial contamination

  • Document al...read more

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Q21. Role of Quality in Aseptic area.

Ans.

Quality plays a critical role in ensuring the sterility and safety of products in aseptic areas.

  • Ensuring compliance with regulatory requirements for aseptic processing

  • Implementing and monitoring aseptic techniques and procedures

  • Performing regular environmental monitoring to detect any contamination

  • Training personnel on proper aseptic practices

  • Investigating and addressing any deviations or failures in aseptic processes

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Q22. Ich guidelines for quality

Ans.

ICH guidelines provide standards for quality in pharmaceuticals.

  • ICH stands for International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use.

  • The guidelines cover topics such as stability testing, impurities, and analytical validation.

  • Adherence to ICH guidelines is often required by regulatory agencies for drug approval.

  • Examples of ICH guidelines include Q1A(R2) for stability testing and Q3C(R6) for impurities.

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Q23. Define all ICH guidelines

Ans.

ICH guidelines are a set of international standards for the development, registration, and post-approval of pharmaceutical products.

  • ICH guidelines cover topics such as clinical trials, quality control, and safety monitoring.

  • Examples of ICH guidelines include E6(R2) Good Clinical Practice, Q9 Quality Risk Management, and M7 Assessment and Control of DNA Reactive (Mutagenic) Impurities in Pharmaceuticals to Limit Potential Carcinogenic Risk.

  • The guidelines are developed by the I...read more

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Q24. What is media fill.

Ans.

Media fill is a simulation test used in pharmaceutical manufacturing to ensure the aseptic filling process is performed correctly.

  • Media fill involves filling sterile growth media instead of actual product to simulate the manufacturing process.

  • The filled containers are then monitored for microbial growth to ensure no contamination occurred.

  • Media fill tests are conducted periodically to validate the aseptic filling process and ensure product sterility.

  • Examples of media fill tes...read more

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