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20+ DMart Interview Questions and Answers

Updated 17 Dec 2024

Q1. Shop floor activities in Production, From Dispensing to packing

Ans.

Shop floor activities in production involve dispensing, manufacturing, packaging, and quality control.

  • Dispensing of raw materials

  • Manufacturing of products

  • Packaging of finished goods

  • Quality control checks throughout the process

  • Cleaning and maintenance of equipment

  • Documentation of all activities

  • Training of personnel

  • Adherence to safety protocols

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Q2. 1-What is machine tell me something about the machine.

Ans.

A machine is a device that uses power to perform a specific task or function.

  • Machines can be found in various industries and sectors, such as manufacturing, transportation, and healthcare.

  • They are designed to automate or assist in tasks that would be difficult or impossible for humans to do.

  • Examples of machines include cars, computers, robots, and medical equipment.

  • Machines can be powered by electricity, fuel, or other energy sources.

  • They often consist of multiple components ...read more

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Q3. Compression machine parameters , and defects identify

Ans.

Compression machine parameters and defects identification

  • Compression machine parameters include force, speed, and displacement

  • Defects can be identified through visual inspection and testing

  • Common defects include cracks, voids, and delamination

  • Testing methods include ultrasonic testing and dye penetrant inspection

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Q4. How are you handling the non moving stock

Ans.

I regularly analyze sales data and identify slow-moving products. I implement strategies to promote these products and reduce inventory.

  • Regularly analyze sales data to identify slow-moving products

  • Implement strategies to promote slow-moving products

  • Offer discounts or bundle deals to incentivize customers to purchase non-moving stock

  • Collaborate with marketing team to create targeted campaigns for slow-moving products

  • Consider returning or exchanging non-moving stock with suppli...read more

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Q5. Telling about types of tablet and it's disintegration limit

Ans.

Tablets can be classified as immediate release, extended release, chewable, effervescent, etc. Disintegration limit varies based on the type of tablet.

  • Immediate release tablets disintegrate within 30 minutes

  • Extended release tablets disintegrate over a longer period of time

  • Chewable tablets disintegrate quickly to aid in swallowing

  • Effervescent tablets disintegrate in water to form a solution

  • Disintegration limit is determined by pharmacopoeial standards

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Q6. What instruments did you handle?

Ans.

I have handled instruments such as calipers, micrometers, spectrophotometers, and pH meters in my previous role as a Quality Control Officer.

  • Calipers

  • Micrometers

  • Spectrophotometers

  • pH meters

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Q7. How to chose dissolution condition for non monograph drug product

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Q8. How u check the receipt of materials

Ans.

To check the receipt of materials, follow a systematic process that includes verifying quantities, inspecting for damages, and comparing with purchase orders.

  • Verify the quantities of materials received match the quantities mentioned in the purchase order.

  • Inspect the materials for any damages or defects.

  • Compare the received materials with the purchase order to ensure accuracy.

  • Check for any discrepancies or missing items and report them to the appropriate department.

  • Maintain pr...read more

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Q9. Various process optimization for pellets technology

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Q10. How to reviews of pvr& pqrs

Ans.

Reviews of PVR and PQRS can be conducted through a systematic process involving data analysis and evaluation.

  • Collect and analyze data related to PVR and PQRS

  • Evaluate the performance and quality based on established criteria

  • Identify areas of improvement and develop action plans

  • Implement changes and monitor the impact

  • Continuously review and update the process to ensure ongoing quality assurance

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Q11. Principle behind to determine the end point in granulation .

Ans.

The principle behind determining the end point in granulation is to achieve the desired particle size and distribution for optimal product performance.

  • The end point in granulation is typically determined by monitoring the particle size distribution using techniques such as sieve analysis or laser diffraction.

  • The desired end point may vary depending on the specific product requirements, such as flowability, compressibility, and dissolution rate.

  • Factors influencing the end poin...read more

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Q12. What is meaning of MHRA

Ans.

MHRA stands for Medicines and Healthcare products Regulatory Agency.

  • MHRA is a regulatory body in the United Kingdom responsible for ensuring that medicines and medical devices are safe and effective.

  • It regulates the safety, quality, and efficacy of medicines and medical devices in the UK.

  • MHRA also monitors and assesses the safety of healthcare products after they have been placed on the market.

  • Examples of MHRA regulated products include prescription medicines, over-the-counte...read more

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Q13. AF 90 T mechanism

Ans.

AF 90 T mechanism is a production executive question.

  • AF 90 T mechanism refers to a specific mechanism used in production.

  • It is important for a production executive to understand and be familiar with this mechanism.

  • Examples of AF 90 T mechanisms could include automated assembly lines or robotic systems used in manufacturing processes.

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Q14. Tell me about tooling

Ans.

Tooling refers to the process of designing and manufacturing tools or equipment used in production.

  • Tooling is essential for manufacturing processes to create products efficiently and accurately.

  • It involves designing and producing molds, dies, jigs, fixtures, and other equipment.

  • Tooling can impact the quality, cost, and speed of production.

  • Examples include injection molds for plastic parts, stamping dies for metal components, and fixtures for assembly processes.

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Q15. How prepared for Leaktest

Ans.

Preparedness for Leaktest involves thorough understanding of procedures, equipment, and safety protocols.

  • Familiarize yourself with the equipment and procedures for conducting a leak test

  • Ensure you understand the safety protocols and precautions to be taken during the test

  • Practice conducting leak tests to become proficient in the process

  • Be prepared to troubleshoot any issues that may arise during the test

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Q16. Tell me about tablet defect

Ans.

Tablet defects are imperfections or issues that can occur during the manufacturing process, affecting the appearance, quality, or performance of the tablet.

  • Common tablet defects include chipping, capping, sticking, and mottling.

  • Chipping refers to the breaking off of small pieces of the tablet edges.

  • Capping occurs when the top or bottom of the tablet separates from the main body.

  • Sticking happens when the tablet material sticks to the punches or dies during compression.

  • Mottling...read more

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Q17. What is granulation end point.

Ans.

Granulation end point is the stage in the granulation process where the desired granule size and shape is achieved.

  • Granulation end point is determined by monitoring the granule size, shape, and moisture content.

  • It is important to reach the granulation end point to ensure uniformity and consistency in the final product.

  • Factors such as binder concentration, mixing time, and drying conditions can affect the granulation end point.

  • Examples of techniques used to determine the granu...read more

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Q18. How to teach camera

Ans.

Teaching camera involves explaining its functions, settings, and techniques for capturing quality photos.

  • Start by explaining the basic functions of the camera such as shutter speed, aperture, and ISO.

  • Demonstrate how to adjust settings to achieve desired effects like depth of field or motion blur.

  • Teach composition techniques like rule of thirds, leading lines, and framing to improve photo quality.

  • Encourage practice and experimentation to develop skills and creativity.

  • Provide f...read more

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Q19. Difference between GC and HPLC

Ans.

GC is used for volatile compounds, while HPLC is used for non-volatile compounds.

  • GC stands for Gas Chromatography, while HPLC stands for High Performance Liquid Chromatography.

  • GC is used for separating and analyzing volatile compounds, such as gases and liquids that can be vaporized without decomposition.

  • HPLC is used for separating and analyzing non-volatile compounds, such as pharmaceuticals, proteins, and carbohydrates.

  • GC typically uses a gas as the mobile phase and a solid...read more

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Q20. Working principle of IR,uv

Ans.

IR and UV spectroscopy are analytical techniques that utilize the absorption of infrared and ultraviolet-visible light to identify and quantify substances.

  • IR spectroscopy measures the absorption of infrared radiation by a sample to identify functional groups in organic molecules.

  • UV spectroscopy measures the absorption of ultraviolet-visible light by a sample to determine the presence of conjugated systems in organic compounds.

  • Both techniques rely on the principle of molecular...read more

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Q21. Expectations of sallay

Ans.

Salary expectations should be based on industry standards, experience, and qualifications.

  • Research industry standards for similar roles

  • Consider your level of experience and qualifications

  • Be prepared to negotiate based on job responsibilities and benefits

  • Provide a range rather than a specific number

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Q22. Saturation solubility process

Ans.

Saturation solubility is the maximum amount of solute that can dissolve in a solvent at a specific temperature.

  • Saturation solubility is influenced by temperature, pressure, and the chemical nature of the solute and solvent.

  • It is typically expressed in units of mass of solute per volume of solvent (e.g. g/L).

  • Factors affecting saturation solubility include the presence of impurities, pH of the solution, and the presence of other solutes.

  • Understanding saturation solubility is im...read more

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Q23. Full form of USFDA?

Ans.

United States Food and Drug Administration

  • USFDA stands for United States Food and Drug Administration

  • It is a federal agency of the Department of Health and Human Services

  • USFDA is responsible for protecting and promoting public health through the regulation and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs, vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emi...read more

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Q24. Capsule filling operation

Ans.

Capsule filling operation involves filling empty capsules with powdered or liquid medication.

  • Capsule filling machines are used to automate the process of filling capsules.

  • The capsules can be filled with various types of medications, such as antibiotics, vitamins, or herbal supplements.

  • Quality control measures are essential to ensure accurate dosing and proper sealing of the capsules.

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Q25. Difference between roi and lod

Ans.

ROI stands for Return on Investment, while LOD stands for Limit of Detection.

  • ROI is a financial metric used to evaluate the efficiency or profitability of an investment.

  • LOD is the lowest concentration of a substance that can be reliably detected by a particular analytical procedure.

  • ROI is typically expressed as a percentage, representing the ratio of net profit to the initial investment.

  • LOD is important in analytical chemistry to determine the sensitivity of an analytical met...read more

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Q26. Principles of hplc, gc, ir

Ans.

Principles of HPLC, GC, and IR involve separation of compounds based on different physical and chemical properties.

  • HPLC (High Performance Liquid Chromatography) separates compounds based on their affinity for the stationary phase and mobile phase.

  • GC (Gas Chromatography) separates compounds based on their boiling points and affinity for the stationary phase.

  • IR (Infrared Spectroscopy) identifies compounds based on their absorption of infrared radiation at specific wavelengths.

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