Alembic Pharmaceuticals
Aye Finance Interview Questions and Answers
Q1. Which type packing is batter in distillation continue?
The type of packing that is better in distillation depends on the specific application and desired outcome.
Structured packing is better for high efficiency and low pressure drop
Random packing is better for high capacity and fouling resistance
Trays are better for high turndown ratio and easy maintenance
Factors to consider include composition of the mixture, desired separation efficiency, pressure drop limitations, and cost
Common types of packing include metal, plastic, and cer...read more
Q2. What is vacuum distillation? How to create vacuum?
Vacuum distillation is a process of separating components of a mixture by boiling it under reduced pressure.
It is used to separate components with high boiling points.
The process involves heating the mixture in a vacuum to lower the boiling point.
The lower pressure also reduces the risk of thermal decomposition.
Vacuum can be created using a vacuum pump or aspirator.
Examples include the separation of crude oil into different fractions and the purification of solvents.
Q3. What is critical process parameter during granulation.
The critical process parameter during granulation is the moisture content of the granules.
Moisture content affects the flowability and compressibility of the granules.
It also impacts the final product quality and stability.
Examples of critical moisture content ranges are 2-4% for wet granulation and 1-3% for dry granulation.
Q4. What will you do if power interruption during wet granulation.
I will immediately stop the wet granulation process, secure the equipment, and address the power interruption before resuming production.
Stop the wet granulation process immediately to prevent any damage to the equipment or product
Secure the equipment to ensure safety and prevent accidents during the power interruption
Address the power interruption by checking the power source, circuit breakers, and contacting maintenance if needed
Resume production only after ensuring that th...read more
Q5. What are yours keys functionality to grow urs organization.
Effective communication, strategic planning, talent development, innovation
Implementing clear communication channels to ensure all team members are aligned with organizational goals
Developing and executing strategic plans to drive growth and achieve objectives
Investing in talent development programs to nurture and retain top performers
Fostering a culture of innovation to stay ahead of competitors and adapt to market changes
Q6. Type of distillation?
There are various types of distillation methods such as simple distillation, fractional distillation, steam distillation, vacuum distillation, etc.
Simple distillation is used to separate liquids with different boiling points
Fractional distillation is used to separate liquids with similar boiling points
Steam distillation is used to extract essential oils from plants
Vacuum distillation is used to distill high boiling point compounds at lower temperatures
Other types of distillat...read more
Q7. Boiling point of solvent
The boiling point of a solvent depends on its chemical composition.
The boiling point of a solvent is the temperature at which it changes from a liquid to a gas.
Solvents with stronger intermolecular forces have higher boiling points.
For example, water has a boiling point of 100°C, while acetone has a boiling point of 56°C.
The boiling point can also be affected by external factors such as pressure.
Knowing the boiling point of a solvent is important for various industrial proces...read more
Q8. What is gmp explain
GMP stands for Good Manufacturing Practice, a set of guidelines ensuring products are consistently produced and controlled according to quality standards.
GMP is a system for ensuring that products are consistently produced and controlled according to quality standards.
It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.
Examples of GMP guidelines include proper sanitation, validation of equi...read more
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