Tatva Chintan Pharma Chem
10+ J K Daga & Associates Interview Questions and Answers
Q1. 3) Method validation and Method development steps?
Method validation and development are crucial steps in ensuring accuracy and reliability of analytical methods.
Method validation involves testing the method to ensure it meets specific criteria for accuracy, precision, specificity, and sensitivity.
Method development involves designing and optimizing a new analytical method to meet specific requirements.
Validation steps include determining the limit of detection, limit of quantification, linearity, accuracy, precision, and spe...read more
Q2. 1) Do you know anything about ADL?
ADL stands for Anti-Defamation League.
ADL is an international Jewish non-governmental organization.
It is dedicated to fighting anti-Semitism and all forms of hate and bigotry.
ADL works to secure justice and fair treatment for all.
They provide education, advocacy, and resources to combat hate crimes and discrimination.
ADL also monitors and exposes extremist groups and activities.
Q3. 4) How to work in pressure or Work load?
To work in pressure or work load, one needs to prioritize tasks, delegate responsibilities, and take breaks when necessary.
Prioritize tasks based on urgency and importance
Delegate responsibilities to team members
Take breaks to avoid burnout and maintain productivity
Use time management techniques such as the Pomodoro technique
Stay organized and maintain clear communication with team members
Q4. 2) Pharma guidelines and Agency?
Pharma guidelines and Agency
Pharma guidelines refer to the set of rules and regulations that pharmaceutical companies must follow in order to ensure the safety and efficacy of their products.
These guidelines are established by regulatory agencies such as the Food and Drug Administration (FDA) in the United States or the European Medicines Agency (EMA) in Europe.
The guidelines cover various aspects including drug development, clinical trials, manufacturing practices, labeling,...read more
Q5. Leakage chemical Drum how much Handle and safely?
Leakage of chemical drums should be handled with caution and following safety protocols.
Assess the situation and identify the type of chemical leaking
Contain the leak by using appropriate materials such as absorbent pads or booms
Wear proper personal protective equipment (PPE) like gloves, goggles, and respirators
Transfer the leaking chemical to a secure container if possible
Dispose of the contaminated materials according to hazardous waste regulations
Q6. Name of chemical in used your company and Unloading Processing?
The chemical used in our company for unloading processing is sulfuric acid.
Sulfuric acid is commonly used in various industries for tasks such as metal cleaning, ore processing, and fertilizer production.
It is a strong mineral acid with the chemical formula H2SO4.
Proper safety measures must be followed when handling sulfuric acid due to its corrosive nature.
Examples of safety measures include wearing appropriate protective gear, ensuring proper ventilation, and having neutral...read more
Q7. How to every working Quality control
Ensure every working quality control by implementing strict procedures, regular training, and continuous monitoring.
Establish clear quality control procedures and guidelines
Provide regular training to employees on quality control standards
Implement regular monitoring and audits to ensure compliance
Utilize quality control tools and software to streamline processes
Encourage feedback and suggestions for improvement from employees
Address any quality control issues promptly and ef...read more
Q8. What Emerson mass flow meter calibration
Emerson mass flow meters can be calibrated using the manufacturer's recommended procedures and tools.
Emerson provides detailed calibration instructions in the product manual or online resources.
Calibration typically involves adjusting the zero and span settings to ensure accurate measurement.
Specialized calibration equipment may be required, such as a reference flow meter or calibration software.
Regular calibration is important to maintain the accuracy and reliability of the ...read more
Q9. Boiling point of solvent
The boiling point of a solvent is the temperature at which it changes from a liquid to a gas.
Boiling point is influenced by factors such as atmospheric pressure and the presence of impurities.
Different solvents have different boiling points.
Boiling point can be used to separate mixtures through distillation.
For example, water has a boiling point of 100 degrees Celsius at sea level.
Q10. PFD &P&ID? Troubleshooting over the process
PFD stands for Process Flow Diagram and P&ID stands for Piping and Instrumentation Diagram. They are essential tools for understanding and troubleshooting processes.
PFD provides a visual representation of the process flow, including equipment and control loops.
P&ID shows the piping, equipment, instrumentation, and control systems in a process.
Both documents are crucial for understanding the process design and identifying potential issues.
Troubleshooting involves analyzing the...read more
Q11. What is gmp
GMP stands for Good Manufacturing Practice. It is a set of guidelines and regulations that ensure the quality and safety of pharmaceutical products.
GMP is a quality management system that covers all aspects of production, from raw materials to finished products.
It includes guidelines for manufacturing processes, equipment, facilities, personnel, documentation, and quality control.
GMP is enforced by regulatory agencies such as the FDA and EMA to ensure that pharmaceutical prod...read more
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