Raptakos Brett and Company
10+ TalkingLands Interview Questions and Answers
Q1. What is the first step for quality maintenance of product?
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
Q2. Process of mfg. of your previous organization.
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
Q3. What is the calibration process for UV and HPLC instruments?
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
Q4. What HACCP? How to do hazard analysis?
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
Q5. Reverse Phase vs Normal Phase Chromatography
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
Q6. Hold on QMS
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.
Q7. What is tablet ?what is Qa ? Difference between Active and excipient?
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
Q8. what is Tablet inprocess
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.
Q9. How to grow business.
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
Q10. What is RO System
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
Q11. What is validation
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
Q12. Need of line clearance
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
Q13. Purpose of stability study
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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