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I applied via Naukri.com and was interviewed in Jul 2023. There were 3 interview rounds.
Assessing new product introduction for cleaning validation involves evaluating the cleaning process, potential residues, and ensuring compliance with regulatory requirements.
Evaluate the cleaning process to ensure it effectively removes any residues from the new product.
Identify potential residues that may be left behind and determine the appropriate cleaning methods to address them.
Ensure that the cleaning validation ...
Critical process parameters for wet granulation include binder type, binder concentration, granulation liquid amount, mixing time, and drying temperature.
Binder type: Determines the binding strength of the granules.
Binder concentration: Affects the granule size and strength.
Granulation liquid amount: Influences the wet massing and granule formation.
Mixing time: Determines the uniformity of the granule size.
Drying tempe
I applied via Referral and was interviewed in May 2021. There were 5 interview rounds.
I applied via Referral and was interviewed before Sep 2021. There were 4 interview rounds.
posted on 25 Feb 2024
I applied via Referral and was interviewed before Feb 2023. There were 2 interview rounds.
CPP parameters refer to Critical Process Parameters which have a significant impact on Critical Quality Attributes (CQA) in manufacturing processes.
CPP parameters are specific process variables that must be controlled within a certain range to ensure product quality.
Examples of CPP parameters include temperature, pressure, flow rate, and mixing speed.
The impact of CPP parameters on CQA can be seen in the final product ...
The annual report submission procedure for USFDA approved products involves compiling data on product performance, safety, and compliance with regulations.
Compile data on product performance, safety, and compliance with USFDA regulations
Submit the annual report to the USFDA within the specified deadline
Include information on any changes in manufacturing processes or product labeling
Ensure all data submitted is accurate
I appeared for an interview in Feb 2022.
Qualification of machine in packing and flow process
Qualification of machine in packing involves testing and validating the machine's performance and capabilities
Flow process includes steps like installation, operational testing, performance testing, and documentation
In my previous company, we followed a qualification protocol that included IQ, OQ, and PQ stages
We also conducted periodic requalification to ensure the m
I applied via Naukri.com and was interviewed before Aug 2021. There were 2 interview rounds.
posted on 20 May 2024
I applied via Naukri.com and was interviewed in Apr 2024. There were 2 interview rounds.
I applied via Naukri.com and was interviewed in Nov 2023. There was 1 interview round.
Recovered amount in accuracy parameter validations is calculated by comparing the actual amount with the expected amount.
Calculate the difference between the actual amount and the expected amount
Verify if the recovered amount falls within an acceptable range of error
Adjust the recovered amount based on any discrepancies found
Document the process and findings for future reference
posted on 29 Sep 2024
Real world evidence case study for Diabetes drug market launch
Systematic literature review
Some of the top questions asked at the Ind-Swift Laboratories Assistant Manager interview -
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Chemist
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