Production Chemist
90+ Production Chemist Interview Questions and Answers
Q1. What is the caps and change control
Caps and change control are processes used in production to ensure quality and consistency.
Caps refers to the specifications and limitations placed on a product or process.
Change control is a system for managing and documenting changes to a product or process.
Caps and change control help maintain quality, regulatory compliance, and consistency in production.
Examples of caps include maximum allowable impurity levels in a pharmaceutical product.
Examples of change control includ...read more
Q2. Lewis acid, pH, acid and base and 5 examples, what is organic chemistry, periodic table, chemical formulas, how to know pH without pH meter.
The interview question covers topics such as Lewis acid, pH, acid and base, organic chemistry, periodic table, chemical formulas, and pH measurement without a pH meter.
Lewis acid is an electron acceptor, examples include AlCl3 and FeCl3
pH is a measure of acidity or basicity, with a range of 0-14
Acids donate H+ ions, bases accept H+ ions
Organic chemistry deals with carbon-based compounds, examples include ethanol and glucose
The periodic table organizes elements by atomic numbe...read more
Production Chemist Interview Questions and Answers for Freshers
Q3. What is vaccum distillation and why is used to vacuum in distillation column?
Vacuum distillation is a process used in distillation columns to lower the boiling point of substances and separate them based on their volatility.
Vacuum distillation is a type of distillation that operates under reduced pressure.
It is used to separate substances with high boiling points or heat-sensitive compounds.
By lowering the pressure, the boiling point of the substances is reduced, allowing for separation at lower temperatures.
Vacuum distillation is commonly used in the...read more
Q4. What is hydrogenation. Which catalyst use How to vent hydrogen gas What do you know about PRV What is vacuum What is vacuum distillation What is capacity of cooling tower and chilling plants
Hydrogenation is a chemical reaction that adds hydrogen to a molecule. Catalysts like nickel, palladium, and platinum are commonly used. Hydrogen gas is vented through a pressure relief valve (PRV). Vacuum distillation is a process that separates components based on their boiling points under reduced pressure. Cooling tower and chilling plant capacity depends on the specific application.
Hydrogenation adds hydrogen to a molecule
Nickel, palladium, and platinum are common cataly...read more
Q5. What is GMP ?,what is change control system ?
GMP stands for Good Manufacturing Practice. Change control system is a process to manage changes in a controlled manner.
GMP is a set of guidelines that ensure the quality and safety of pharmaceutical products.
It covers all aspects of production, from raw materials to finished products.
Change control system is a process to manage changes in a controlled manner.
It involves documenting and reviewing proposed changes, assessing their impact, and implementing them in a controlled ...read more
Q6. How will handle chlorine gas if certainaly increase pressure?
To handle increased pressure of chlorine gas, follow safety protocols, use appropriate equipment, and ensure proper ventilation.
Follow safety protocols and guidelines for handling chlorine gas
Use appropriate personal protective equipment (PPE) such as gloves, goggles, and a respirator
Ensure proper ventilation in the area to prevent the accumulation of chlorine gas
If pressure increases, avoid sudden release and slowly release the pressure using a controlled method
Consider usin...read more
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Q7. Do you know how to use EDMs and Trackwise??
Yes, I am familiar with using EDMs and Trackwise.
I have experience using EDMs (Electronic Document Management Systems) to store and manage production-related documents.
I am proficient in using Trackwise, a software used for tracking and managing quality and compliance processes.
I can navigate through EDMs to retrieve and update documents as needed.
I can utilize Trackwise to initiate and track production-related workflows, such as change control or deviation management.
I am co...read more
Q8. WASHING AREA DOOR OPEN SIDE AND WHY ? Humidity limits ? Critical parameter of process? Universal solute
The washing area door should open towards the outside to prevent contamination and improve air circulation.
Opening the door towards the outside prevents contamination from entering the washing area.
It also improves air circulation and reduces humidity levels, which can be critical parameters for some processes.
Universal solute is not relevant to the washing area door orientation.
Production Chemist Jobs
Q9. What is the BMS and bpr
BMS stands for Batch Manufacturing Record and BPR stands for Batch Production Record.
BMS is a document that contains detailed instructions for the production of a specific batch of a product.
It includes information about the raw materials, equipment, manufacturing steps, and quality control tests.
BPR is a record that documents the actual production data and results obtained during the manufacturing process.
It provides a detailed account of the batch production, including devi...read more
Q10. What is the gmp and cgmp
GMP stands for Good Manufacturing Practice, which ensures that products are consistently produced and controlled according to quality standards.
GMP is a set of guidelines and regulations that ensure the quality and safety of pharmaceutical and healthcare products.
GMP covers various aspects of production, including facilities, equipment, personnel, documentation, and processes.
GMP emphasizes the importance of quality control, traceability, and risk management.
CGMP specifically...read more
Q11. Do you know how to prepare BMR & BCR?
Yes, I know how to prepare BMR & BCR.
BMR stands for Batch Manufacturing Record, which is a document that provides detailed instructions for the production of a specific batch of a product.
BCR stands for Batch Control Record, which is a document that records the actual production data and results obtained during the manufacturing process.
Preparing BMR involves gathering all the necessary information and instructions for the production process, including formulation, equipment,...read more
Q12. What is the production
Production refers to the process of creating goods or services through various stages of manufacturing or assembly.
Production involves transforming raw materials or components into finished products.
It includes activities such as planning, sourcing, manufacturing, quality control, and distribution.
Production chemists play a crucial role in developing and optimizing chemical processes for manufacturing pharmaceuticals, chemicals, or other products.
They ensure the production pr...read more
Q13. Define about heat transfer, mass transfer, Heat exchanger, viscosity, pH scale, temperature based questions, fluid flow and types of flow, dryer, resins.
Explanation of heat transfer, mass transfer, heat exchanger, viscosity, pH scale, fluid flow, dryer, and resins.
Heat transfer is the movement of thermal energy from one object to another.
Mass transfer is the movement of a substance from one location to another.
Heat exchanger is a device used to transfer heat between two or more fluids.
Viscosity is a measure of a fluid's resistance to flow.
pH scale is a measure of the acidity or basicity of a solution.
Fluid flow can be laminar...read more
Q14. Why is acid stored in glass container not in iron container ?
Acid is stored in glass containers instead of iron containers to prevent chemical reactions that could contaminate the acid or cause dangerous reactions.
Glass is non-reactive with most acids, preventing contamination of the acid.
Iron containers can react with acids, leading to the formation of potentially dangerous byproducts.
Glass containers are more chemically inert and do not corrode when in contact with acids.
Using glass containers helps maintain the purity and stability ...read more
Q15. How many types of reactors followed.
There are several types of reactors used in production chemistry.
Batch reactors
Continuous stirred-tank reactors (CSTR)
Plug flow reactors (PFR)
Fixed-bed reactors
Fluidized-bed reactors
Membrane reactors
Photochemical reactors
Electrochemical reactors
Q16. How will you make the document if no product is prepared correctly
I would thoroughly review the production process, identify the root cause of the errors, and implement corrective actions to ensure correct product preparation in the future.
Conduct a detailed review of the production procedures and protocols
Identify any deviations or mistakes in the preparation process
Investigate the root cause of the errors, such as equipment malfunction or human error
Implement corrective actions to prevent similar mistakes in the future, such as additional...read more
Q17. What is DT and Dissolution test
DT stands for Dissolution Test, which is a method used to determine the rate at which a drug substance dissolves in a specific medium.
DT is an abbreviation for Dissolution Test.
It is a standard method used in the pharmaceutical industry to evaluate the release of active pharmaceutical ingredients from solid dosage forms.
The test involves placing a dosage form in a dissolution medium and measuring the amount of drug substance that dissolves over time.
The results of the test he...read more
Q18. What is sterilization and it's type?
Sterilization is the process of killing or eliminating all forms of microorganisms, including bacteria, viruses, and fungi.
Sterilization is essential in various industries, including healthcare, pharmaceuticals, and food production.
There are different types of sterilization methods, such as heat sterilization, chemical sterilization, and radiation sterilization.
Heat sterilization involves using high temperatures to kill microorganisms. Autoclaving is a common heat sterilizati...read more
Q19. Difference between disintegration test and dissolution test?
Disintegration test measures the time it takes for a tablet to break down, while dissolution test measures the rate at which the drug is released from the tablet.
Disintegration test evaluates the physical breakdown of a tablet into smaller particles.
Dissolution test evaluates the release of the drug substance from the tablet.
Disintegration test is a measure of tablet disintegration time, while dissolution test is a measure of drug release rate.
Disintegration test is performed...read more
Q20. Do you know to formulate new ayurvedic medicines?
Yes, I have experience in formulating new ayurvedic medicines.
I have a deep understanding of Ayurvedic principles and herbs
I have formulated several ayurvedic medicines in my previous roles
I keep myself updated with the latest research and developments in Ayurveda
Q21. Heat stability of grade specific gravity of grade viscosity of the grader
The question is unclear and lacks context.
The interviewer needs to provide more information or rephrase the question.
It is unclear what is meant by 'grader' and what specific product or material is being referred to.
Without more information, it is difficult to provide a meaningful answer.
Q22. Tell me the name of all the strong acid and strong base
Strong acids and bases are substances that completely dissociate in water to release H+ or OH- ions.
Strong acids include hydrochloric acid (HCl), sulfuric acid (H2SO4), and nitric acid (HNO3)
Strong bases include sodium hydroxide (NaOH), potassium hydroxide (KOH), and calcium hydroxide (Ca(OH)2)
Q23. Full form of GMP, what is SOP?
GMP stands for Good Manufacturing Practice. SOP stands for Standard Operating Procedure.
GMP is a set of guidelines that ensure the quality and safety of pharmaceutical products.
SOP is a document that outlines the steps to be followed in a particular process to ensure consistency and quality.
GMP and SOP are both important in the pharmaceutical industry to maintain quality and safety standards.
Examples of SOPs include procedures for cleaning equipment, handling raw materials, a...read more
Q24. Which type of company and details of product and turnover of industries
I have experience working in the pharmaceutical industry with a focus on drug production and quality control.
Worked in pharmaceutical companies producing a range of drugs for various medical conditions
Experience in ensuring compliance with regulatory standards such as FDA guidelines
Involved in the production and testing of pharmaceutical products to ensure quality and efficacy
Q25. Boiling and melting point of water and other solvents.
Water has a boiling point of 100°C and a melting point of 0°C. Other solvents have varying boiling and melting points.
Water has a high boiling point due to its strong hydrogen bonding
Solvents like ethanol have lower boiling points than water
Melting points of solvents depend on their molecular structure
Some solvents like mercury are liquid at room temperature
Boiling and melting points are important in chemical reactions and purification processes
Q26. What is your current and expected CTC?
I am currently earning X amount and my expected CTC is Y amount.
Mention your current salary and expected CTC separately
Be honest and realistic about your expectations
Research the industry standards and salary range for the position
Consider other benefits and perks besides salary
Example: My current CTC is 5 lakhs per annum and I am expecting a hike of 15-20% in my next role.
Example: I am currently earning 8 lakhs per annum and after researching the industry standards, I am exp...read more
Q27. What is pump and principal working and pump part name
A pump is a device that moves fluids (liquids or gases) by mechanical action. The principal working involves creating a pressure difference to push the fluid through a system.
Pump parts include impeller, casing, shaft, bearings, and seals
Examples of pumps include centrifugal pumps, diaphragm pumps, and gear pumps
The principal working of a pump involves converting mechanical energy into fluid flow
Q28. How much vacuum build in Hyderabad
The vacuum build in Hyderabad varies depending on the location and time of measurement.
Vacuum levels in Hyderabad can range from 700 to 760 mmHg
Factors such as altitude, weather conditions, and equipment used can affect vacuum levels
For example, in a laboratory setting, a vacuum pump may be used to create a vacuum for experiments
Q29. Define narcotic and non alangesic substay
A narcotic is a drug that induces sleep or dulls the senses, while a non-analgesic substance does not provide pain relief.
Narcotics are often used as painkillers or sedatives.
Examples of narcotics include morphine, codeine, and heroin.
Non-analgesic substances do not have pain-relieving properties.
Examples of non-analgesic substances include antibiotics, antacids, and vitamins.
Q30. how can handle all query ?
Handling all queries requires effective communication, organization, and problem-solving skills.
Develop good communication skills to understand and address queries effectively.
Stay organized by keeping track of queries and prioritizing them based on urgency.
Utilize problem-solving skills to find solutions and provide accurate information.
Be proactive in seeking help or guidance when needed.
Maintain a positive and professional attitude while handling queries.
Examples: Respondi...read more
Q31. How to handle the safety
To handle safety in production, it is important to follow safety protocols, conduct regular inspections, provide proper training, and maintain a clean and organized work environment.
Follow safety protocols and guidelines provided by the company and regulatory bodies.
Conduct regular inspections to identify and address any potential safety hazards.
Provide proper training to all employees on safety procedures and protocols.
Maintain a clean and organized work environment to minim...read more
Q32. What is a different between acid and basic
Acids have a pH less than 7 and can donate protons, while bases have a pH greater than 7 and can accept protons.
Acids have a pH less than 7, while bases have a pH greater than 7
Acids can donate protons, while bases can accept protons
Acids taste sour, while bases taste bitter
Examples of acids include hydrochloric acid (HCl) and sulfuric acid (H2SO4)
Examples of bases include sodium hydroxide (NaOH) and ammonia (NH3)
Q33. How to use manpower utility.
Manpower utility is used to effectively manage and utilize the workforce in production operations.
Identify the required manpower for each task or operation
Allocate the manpower based on their skills and availability
Monitor and track the performance and productivity of the workforce
Optimize the utilization of manpower by adjusting schedules and workload
Ensure proper training and development of the workforce
Implement strategies to motivate and engage the workforce
Regularly revi...read more
Q34. What are the safety equipment you will be used?
Safety equipment used includes gloves, goggles, lab coat, and closed-toe shoes.
Gloves are used to protect hands from chemicals and other hazards.
Goggles are worn to protect eyes from splashes and fumes.
Lab coat is worn to protect clothing from spills and splashes.
Closed-toe shoes are important to protect feet from spills and falling objects.
Q35. How to open vacuum tray dryer.
To open a vacuum tray dryer, follow these steps carefully.
Ensure the vacuum tray dryer is turned off and disconnected from power source.
Release any pressure inside the dryer by slowly opening the vent valve.
Unlock and open the door of the vacuum tray dryer.
Carefully remove the trays one by one, starting from the top.
Inspect the trays for any residue or product buildup and clean if necessary.
Close the door securely after removing or loading trays.
Reconnect the power source and...read more
Q36. Preparation method of chyawanprash Compression of tablet hardness d.t. And composition of products
Chyawanprash is prepared by mixing various herbs and spices with a base of amla fruit pulp and honey.
Chyawanprash is a traditional Ayurvedic herbal jam
Ingredients include amla fruit pulp, ghee, honey, and a variety of herbs and spices
The mixture is cooked over low heat for several hours
Tablet hardness is determined by the compression force applied during manufacturing
Composition of products may vary depending on the manufacturer
Q37. What is reactor and it's function?
A reactor is a vessel used for chemical reactions, where reactants are converted into products under controlled conditions.
Reactor is used in chemical and pharmaceutical industries for various processes such as synthesis, fermentation, and polymerization.
It can be of different types such as batch, continuous, and semi-batch reactors.
The function of a reactor is to provide a controlled environment for the chemical reaction to take place, such as temperature, pressure, and mixi...read more
Q38. Work permit system types of permitts
Work permit system includes hot work, confined space, electrical, excavation, and others.
Hot work permit is required for any work involving open flames or sparks
Confined space permit is required for work in enclosed spaces with limited entry and exit points
Electrical permit is required for work on electrical systems or equipment
Excavation permit is required for any work involving digging or excavation
Other types of permits may include working at heights, hazardous materials, ...read more
Q39. How to operate reactors
Reactors are operated by following standard operating procedures, monitoring key parameters, adjusting conditions as needed, and ensuring safety protocols are followed.
Follow standard operating procedures provided by the manufacturer or company
Monitor key parameters such as temperature, pressure, flow rate, and pH regularly
Adjust conditions as needed to maintain desired reaction conditions
Ensure safety protocols are followed at all times to prevent accidents
Keep detailed reco...read more
Q40. What is exothermic reaction
An exothermic reaction is a chemical reaction that releases energy in the form of heat.
Exothermic reactions release heat to the surroundings
They have a negative change in enthalpy (ΔH)
Examples include combustion reactions, neutralization reactions, and some oxidation reactions
Q41. DT time of tablet and capsule
DT time refers to the disintegration time of tablets and capsules.
DT time is the time it takes for a tablet or capsule to disintegrate in the body.
It is an important parameter in pharmaceutical manufacturing to ensure proper drug release.
Different tablets and capsules may have different DT times depending on their formulation and design.
DT time can be influenced by factors such as the type of excipients used, the compression force during tablet manufacturing, and the coating ...read more
Q42. How many batch change in reactor
The number of batch changes in a reactor can vary depending on the production schedule and process requirements.
The number of batch changes in a reactor is typically determined by the production plan and the capacity of the reactor.
Factors such as reaction time, temperature, pressure, and product yield can also influence the frequency of batch changes.
For example, a reactor used for continuous production may have fewer batch changes compared to a reactor used for batch produc...read more
Q43. How many types of vacuum pump are there
There are two main types of vacuum pumps: gas transfer pumps and entrapment pumps.
Gas transfer pumps: move gas molecules through the pump using positive displacement or momentum transfer (e.g. rotary vane pump, diaphragm pump)
Entrapment pumps: capture gas molecules by adsorption or condensation on a solid surface (e.g. cryopump, ion pump)
Q44. How do you convert 750 ml water into kg
To convert 750 ml of water into kg, you need to know the density of water.
1 ml of water weighs approximately 1 gram
1 kg is equal to 1000 grams
Therefore, 750 ml of water is equal to 0.75 kg
Q45. What is specific gravity of water
Specific gravity of water is 1.0, indicating that it is denser than air and most other liquids.
Specific gravity of water is always 1.0 at standard conditions
It is a unitless quantity that compares the density of water to the density of a reference substance
Specific gravity of water is used in various industries including chemistry, engineering, and brewing
Q46. Which are poore solvents?
Poor solvents are those that cannot dissolve a wide range of solutes.
Poor solvents have low polarity and weak intermolecular forces.
Examples of poor solvents include hexane, benzene, and toluene.
Poor solvents are often used in chromatography to separate compounds based on their polarity.
They are also used in polymerization reactions to control the size and shape of the resulting polymer.
Poor solvents can be contrasted with good solvents, which have high polarity and strong in...read more
Q47. What is ALCOA ?
ALCOA is an acronym that stands for Attributable, Legible, Contemporaneous, Original, and Accurate.
ALCOA is a set of principles used in the pharmaceutical industry to ensure data integrity.
Attributable means that all data should be traceable to the person who generated it.
Legible means that the data should be clear and easy to read.
Contemporaneous means that the data should be recorded at the time of the activity.
Original means that the data should be the first recording of t...read more
Q48. In emercy swich vacation in form
The question is unclear and seems to contain a typo.
The question is not clear and may contain a typo.
It is difficult to provide a descriptive answer without understanding the question properly.
Please clarify the question or provide more context.
Q49. You know api plant and formulation plant different
API plant is where active pharmaceutical ingredients are manufactured, while formulation plant is where these ingredients are formulated into final products.
API plant focuses on manufacturing active pharmaceutical ingredients
Formulation plant focuses on formulating these ingredients into final products
API plant requires specialized equipment and processes for synthesis
Formulation plant requires equipment for blending, granulation, and tableting
Example: API plant may produce p...read more
Q50. Equipment standard operating procedure
Equipment standard operating procedure is a set of instructions for safe and efficient use of equipment.
Equipment SOP should include step-by-step instructions for operation, maintenance, and troubleshooting.
It should also include safety precautions and emergency procedures.
Regular training and updates should be provided to ensure compliance and effectiveness.
Examples of equipment SOPs include those for laboratory instruments, manufacturing machinery, and medical devices.
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