
Aurobindo Pharma


10+ Aurobindo Pharma Executive Interview Questions and Answers
Q1. What are the type of sensor used in your company?
We use a variety of sensors including temperature, pressure, humidity, and motion sensors.
Temperature sensors are used to monitor the temperature of equipment and environments.
Pressure sensors are used to measure pressure in systems such as pipelines and tanks.
Humidity sensors are used to measure the amount of moisture in the air.
Motion sensors are used to detect movement in areas where security is a concern.
Other sensors we use include light sensors, proximity sensors, and g...read more
Q2. Abbreviations of all equipment and data entegrete and procedures
It is not possible to provide abbreviations for all equipment, data integration, and procedures in a single answer.
Abbreviations vary by industry and field
Equipment and data integration abbreviations may include acronyms such as ERP, CRM, and IoT
Medical field abbreviations may include EKG, MRI, and CT
Procedures may have abbreviations such as CPR, ACLS, and PALS
Q3. How vaccum pumps are used and process
Vacuum pumps are used to create a vacuum by removing gas molecules from a sealed chamber or container.
Vacuum pumps are used in various industries such as food packaging, semiconductor manufacturing, and medical research.
The process involves creating a low-pressure environment by removing air or gas molecules from a sealed container.
There are different types of vacuum pumps such as rotary vane pumps, diaphragm pumps, and scroll pumps.
Examples of vacuum pump applications includ...read more
Q4. What is RTD?
RTD stands for Resistance Temperature Detector.
RTD is a type of temperature sensor that measures temperature by detecting changes in electrical resistance.
It is commonly used in industrial and scientific applications where accuracy and stability are important.
Platinum is a common material used in RTDs due to its high accuracy and stability.
RTDs can be found in various forms such as wire-wound, thin-film, and coiled elements.
They are often used in conjunction with temperature ...read more
Q5. why always c letter small in cGMP Guidelines ?
The 'c' in cGMP guidelines is always lowercase because it stands for 'current', not a proper noun.
The 'c' in cGMP stands for 'current', not a proper noun.
Lowercase 'c' emphasizes that the guidelines are constantly evolving and being updated.
It distinguishes cGMP guidelines from other specific guidelines or regulations.
Example: cGMP guidelines are designed to ensure the quality and safety of pharmaceutical products.
Q6. What is the cleaning validation?
Cleaning validation is the process of ensuring that equipment and facilities used in manufacturing are properly cleaned to prevent contamination.
Cleaning validation is a critical part of Good Manufacturing Practices (GMP) in industries such as pharmaceuticals, biotechnology, and medical devices.
It involves testing and verifying that the cleaning process effectively removes any residues or contaminants from the equipment or facility.
Validation protocols must be developed and e...read more
Q7. The working principles of air conditioning
Air conditioning works by removing heat and moisture from the air, and then circulating cool, dry air back into the room.
Air is drawn into the unit through a filter
The air is cooled by passing over evaporator coils filled with refrigerant
The cooled air is then circulated back into the room through ducts or vents
Moisture is removed from the air through condensation
The warm, moist air is then expelled outside through a separate vent or duct
Q8. What action you take when Media Fail ?
When media fails, I assess the situation, communicate with stakeholders, and take appropriate corrective actions.
Assess the impact of the media failure on the organization
Communicate transparently with stakeholders about the situation
Identify the root cause of the failure and take corrective actions
Implement measures to prevent similar failures in the future
Q9. Ehs key role play as a safety hod
The safety head plays a crucial role in ensuring the safety of employees and compliance with safety regulations.
Developing and implementing safety policies and procedures
Conducting safety training for employees
Performing safety audits and inspections
Investigating accidents and incidents and implementing corrective actions
Ensuring compliance with safety regulations and standards
Collaborating with management and employees to promote a culture of safety
Q10. Difference between API, BULK, and Formulation ?
API is the active ingredient in a drug, BULK is the raw material used to make the drug, and Formulation is the final product with the API and other ingredients.
API stands for Active Pharmaceutical Ingredient, it is the main ingredient in a drug responsible for its therapeutic effect (e.g. acetaminophen in Tylenol)
BULK refers to the raw materials used to manufacture the drug, such as excipients, binders, and fillers
Formulation is the final product that contains the API along w...read more
Q11. Explain about ALCOA ++. and GDP.?
ALCOA++ is a data integrity framework used in regulated industries, while GDP refers to Gross Domestic Product.
ALCOA++ is a framework used in regulated industries to ensure data integrity, standing for Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, and Enduring.
GDP is a measure of a country's economic performance, representing the total value of all goods and services produced over a specific time period within a country's borders.
ALCOA++ is...read more
Q12. What is the CAPA?
CAPA stands for Corrective and Preventive Action. It is a process used to identify and address problems in a systematic way.
CAPA is a quality management system used in various industries to identify and address problems.
It involves investigating the root cause of a problem and implementing corrective and preventive actions to prevent it from happening again.
CAPA is often used in the medical field to ensure patient safety and compliance with regulations.
Examples of CAPA includ...read more
Q13. Types of Validation
Validation is the process of checking the accuracy and integrity of data or information.
Data validation ensures that data is accurate, complete, and consistent.
There are different types of validation, including format validation, range validation, and logic validation.
Format validation checks if data follows a specific format, such as a valid email address or phone number.
Range validation verifies if data falls within a specified range, like checking if an age is between 18 a...read more
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