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Intas Pharmaceuticals
Proud winner of ABECA 2024 - AmbitionBox Employee Choice Awards
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I applied via Walk-in and was interviewed in Oct 2021. There were 4 interview rounds.
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I applied via Naukri.com and was interviewed before Jun 2022. There were 3 interview rounds.
posted on 16 May 2024
I applied via Company Website and was interviewed in Apr 2024. There were 2 interview rounds.
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I applied via Walk-in and was interviewed in Jun 2023. There were 3 interview rounds.
posted on 25 Mar 2024
I applied via LinkedIn and was interviewed before Mar 2023. There was 1 interview round.
Validation is the process of ensuring that a product or service meets the requirements and specifications. In-process sampling is a method of monitoring and testing a product during the manufacturing process.
Validation ensures that a product or service meets the requirements and specifications
In-process sampling is a method of monitoring and testing a product during the manufacturing process
Validation is done before th...
I applied via Naukri.com and was interviewed before Jun 2022. There were 3 interview rounds.
posted on 16 Aug 2021
I applied via Naukri.com and was interviewed in Jun 2022. There were 2 interview rounds.
Parameters of compressed air validation include purity, pressure, dew point, particle count, and microbial content.
Purity: Ensure absence of contaminants such as oil, water, and particles.
Pressure: Confirm air pressure meets specified requirements.
Dew Point: Measure moisture content to prevent corrosion and freezing.
Particle Count: Verify air cleanliness by counting particles of various sizes.
Microbial Content: Test fo...
Equipment qualification process ensures that equipment is suitable for its intended use by following a systematic approach.
Define equipment requirements and specifications
Select appropriate equipment based on requirements
Install and set up equipment according to manufacturer's guidelines
Perform operational and performance qualification tests
Document all qualification activities and results
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