ICS Instrumentation & Control Solution
10+ Kalyan Toll Infrastructure Interview Questions and Answers
Q1. Do you know about discrepancy and how to use.
Discrepancy refers to a difference or inconsistency between two or more pieces of information. It is used to identify and resolve errors or inconsistencies in data.
Discrepancy is commonly used in quality control and validation processes.
It can be identified through comparing data from different sources or through manual review.
Examples of discrepancies include mismatched data, missing information, or conflicting data.
Discrepancies should be resolved before finalizing data or ...read more
Q2. Do you perform any validation activity.
Yes, I perform validation activities as part of my job responsibilities.
I am responsible for ensuring that all processes and systems meet regulatory requirements.
I conduct validation tests and document the results.
I work closely with cross-functional teams to identify and address any issues that arise during the validation process.
Examples of validation activities I have performed include software validation, equipment validation, and process validation.
Q3. What is 21 CFR Part 11.
21 CFR Part 11 is a regulation by the FDA that defines the criteria under which electronic records and electronic signatures are considered trustworthy, reliable, and equivalent to paper records.
21 CFR Part 11 applies to electronic records and electronic signatures used in FDA-regulated industries, such as pharmaceuticals, medical devices, and biologics.
It requires that electronic records be secure, accurate, and accessible, and that electronic signatures be unique, verifiabl...read more
Q4. Tell me the Validation deliverables.
Validation deliverables include validation plan, protocols, reports, and summary.
Validation Plan: outlines the scope, approach, and resources for validation
Validation Protocols: documents the testing procedures and acceptance criteria
Validation Reports: summarizes the results of testing and any deviations from acceptance criteria
Validation Summary: provides an overall assessment of the validation process and results
Q5. Tell me about GAMP 5 category.
GAMP 5 is a category for software validation in the pharmaceutical and biotech industries.
GAMP 5 stands for Good Automated Manufacturing Practice 5.
It provides guidelines for the validation of automated systems in the pharmaceutical and biotech industries.
It categorizes software based on its impact on product quality and patient safety.
The categories range from Category 1 (low impact) to Category 5 (high impact).
Examples of Category 5 software include systems that control cri...read more
Q6. Why are we perform validation.
Validation ensures that a product or process meets the required standards and specifications.
To ensure safety and efficacy of products
To comply with regulatory requirements
To minimize risks and errors
To improve quality and reliability
To gain customer trust and confidence
Q7. What is difference between DCS and SCADA?
DCS is used for controlling processes in industries, while SCADA is used for monitoring and controlling processes in real-time.
DCS stands for Distributed Control System, used for controlling processes in industries.
SCADA stands for Supervisory Control and Data Acquisition, used for monitoring and controlling processes in real-time.
DCS is typically used in industries such as oil and gas, power plants, and manufacturing.
SCADA is commonly used in industries like water treatment ...read more
Q8. What is the working principle of relay?
Relays work on the principle of electromagnetic attraction and repulsion to control the flow of current in a circuit.
Relays have an electromagnet which attracts an armature to make or break electrical contacts.
When current flows through the coil of the relay, it creates a magnetic field that pulls the armature towards it, closing the contacts.
When the current stops, the magnetic field disappears, and the spring returns the armature to its original position, opening the contac...read more
Q9. GAMP 5 software categories
GAMP 5 software categories are defined by the level of impact on product quality and patient safety.
Category 1: Infrastructure software
Category 2: Non-configured software
Category 3: Configured software
Category 4: Bespoke software
Category 5: Legacy software
Each category has different requirements for validation and testing.
Examples of software in each category include operating systems, off-the-shelf software, and custom-built applications.
Q10. Restricting edit of data and modifications
Q11. What is the RTD and working
RTD stands for Resistance Temperature Detector, which is a temperature sensor that operates on the principle that the electrical resistance of a metal changes with temperature.
RTD is commonly used in industrial applications for temperature measurement.
It provides accurate and stable temperature readings.
RTDs are made of pure metals like platinum, nickel, or copper.
The resistance of the RTD changes linearly with temperature, allowing for precise temperature measurements.
RTDs a...read more
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