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Raptakos Brett and Company

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10+ TalkingLands Interview Questions and Answers

Updated 2 Jan 2025

Q1. What is the first step for quality maintenance of product?

Ans.

The first step for quality maintenance of product is to establish a quality management system.

  • Establishing quality objectives and policies

  • Identifying and documenting processes and procedures

  • Implementing quality control measures

  • Training employees on quality standards

  • Regularly monitoring and evaluating the system

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Q2. Process of mfg. of your previous organization.

Ans.

The manufacturing process involved multiple stages including raw material procurement, quality checks, production, packaging, and final inspection.

  • Raw material procurement from approved vendors

  • Quality checks at every stage of production

  • Production process involved mixing, blending, and filling

  • Packaging of finished products in appropriate containers

  • Final inspection to ensure product meets quality standards

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Q3. What is the calibration process for UV and HPLC instruments?

Ans.

Calibration process for UV and HPLC instruments involves setting up reference standards, adjusting parameters, and verifying accuracy.

  • Prepare reference standards for UV and HPLC analysis

  • Adjust wavelength, detector sensitivity, and flow rate for UV instrument

  • Run standard solutions to verify accuracy and make necessary adjustments

  • Perform system suitability tests to ensure instrument performance meets requirements

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Q4. What HACCP? How to do hazard analysis?

Ans.

HACCP is a food safety management system. Hazard analysis involves identifying potential hazards and implementing controls to prevent them.

  • HACCP stands for Hazard Analysis and Critical Control Points

  • It is a systematic approach to identifying and controlling food safety hazards

  • Hazard analysis involves identifying potential hazards and assessing their likelihood and severity

  • Controls are then implemented to prevent or reduce the likelihood of hazards occurring

  • Examples of hazards...read more

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Q5. Reverse Phase vs Normal Phase Chromatography

Ans.

Reverse phase chromatography uses a non-polar stationary phase and a polar mobile phase, while normal phase chromatography uses a polar stationary phase and a non-polar mobile phase.

  • Reverse phase chromatography is more commonly used in analytical chemistry for separating non-polar compounds, while normal phase chromatography is used for polar compounds.

  • In reverse phase chromatography, the more non-polar compounds elute first, while in normal phase chromatography, the more pol...read more

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Q6. Hold on QMS

Ans.

QMS stands for Quality Management System.

  • QMS is a set of policies, processes, and procedures implemented to ensure that products and services meet quality standards.

  • It includes activities such as quality planning, quality control, quality assurance, and quality improvement.

  • QMS helps organizations achieve customer satisfaction, comply with regulations, and continuously improve their processes.

  • Examples of QMS frameworks include ISO 9001, Six Sigma, and Lean Manufacturing.

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Q7. What is tablet ?what is Qa ? Difference between Active and excipient?

Ans.

A tablet is a solid dosage form of medication that is compressed into a small, flat shape. QA stands for Quality Assurance.

  • A tablet is a pharmaceutical dosage form that contains an active ingredient and excipients.

  • It is a solid form of medication that is compressed into a small, flat shape.

  • Tablets are commonly used for oral administration.

  • QA (Quality Assurance) is a process that ensures the quality of a product or service.

  • In the context of pharmaceuticals, QA in tablet manufa...read more

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Q8. what is Tablet inprocess

Ans.

Tablet inprocess refers to the stage in pharmaceutical manufacturing where tablets are being produced but have not yet completed all necessary steps.

  • Tablet inprocess involves the mixing of active pharmaceutical ingredients with excipients.

  • Tablet inprocess includes the compression of the mixture into tablet form.

  • Tablet inprocess may also involve coating the tablets for aesthetic or functional purposes.

  • Examples: blending of ingredients, tablet compression, coating process.

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Q9. How to grow business.

Ans.

Growing business involves strategic planning, market research, customer engagement, and continuous improvement.

  • Develop a comprehensive business plan outlining goals, strategies, and tactics.

  • Conduct market research to identify opportunities, trends, and competition.

  • Engage with customers to understand their needs and preferences.

  • Invest in marketing and advertising to reach a wider audience.

  • Focus on product/service quality and customer satisfaction.

  • Implement feedback loops for c...read more

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Q10. What is RO System

Ans.

RO system is a water treatment process that uses a semi-permeable membrane to remove impurities from water.

  • RO stands for Reverse Osmosis

  • It uses a semi-permeable membrane to remove impurities from water

  • It is commonly used in water treatment plants to produce clean drinking water

  • RO systems can remove up to 99% of dissolved salts, minerals, and other impurities from water

  • Examples of impurities removed by RO systems include lead, arsenic, fluoride, and nitrates

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Q11. What is validation

Ans.

Validation is the process of ensuring that a product or system meets the requirements and specifications set for it.

  • Validation confirms that the product meets the customer's needs and expectations

  • It involves testing the product under real-world conditions

  • Validation is often done at the end of the development process to ensure the product is ready for release

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Q12. Need of line clearance

Ans.

Line clearance is necessary to prevent cross-contamination and ensure product quality by verifying that the production area is clean and ready for the next batch.

  • Prevents cross-contamination between different products or batches

  • Verifies that the production area is clean and free of any residues

  • Ensures that equipment is properly sanitized before starting a new batch

  • Confirms that all materials and components are in the correct place and properly labeled

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Q13. Purpose of stability study

Ans.

Stability studies are conducted to evaluate the shelf life and storage conditions of a product.

  • Stability studies help determine how long a product can be stored without significant changes in quality or efficacy.

  • They are important for establishing expiration dates and storage instructions.

  • Factors such as temperature, humidity, light exposure, and packaging materials are considered in stability studies.

  • Results of stability studies are used to support product registration and r...read more

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