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I applied via Naukri.com and was interviewed in Jun 2024. There were 3 interview rounds.
Yes, sugar syrup can be filtered through Sivtec filter instead of filter press.
Sivtec filter can be used for filtering sugar syrup as it is designed to handle various types of liquids and slurries.
Sivtec filter offers a more efficient and cost-effective filtration process compared to filter press.
Sivtec filter can provide a higher throughput and better filtration quality for sugar syrup.
Using Sivtec filter for sugar sy...
Product failure in quality can be attributed to various factors such as inadequate resources, poor quality control measures, lack of skilled workforce, and outdated technology.
Inadequate resources such as insufficient funding for quality control measures or lack of access to high-quality materials can lead to product failure.
Poor quality control measures, such as lack of regular inspections or testing, can result in de...
Manpower handling and manufacturing packing process mapping involves organizing and optimizing the workforce and packaging procedures.
Analyze current manpower allocation and packaging processes
Identify areas for improvement in efficiency and productivity
Create a detailed map of manpower roles and responsibilities in the packing process
Implement changes to streamline operations and reduce waste
Regularly review and updat
Yes, deviations occasionally occur during operations and are promptly addressed through effective communication and problem-solving.
Identify the root cause of the deviation
Communicate the deviation to relevant team members
Collaborate with team to develop a solution
Implement corrective actions to prevent future deviations
Validation batches are planned based on regulatory requirements and company standards. Quality and micro testing are conducted to ensure product safety and efficacy.
Validation batches are planned according to regulatory guidelines and company protocols.
Quality testing is performed to assess the product's physical, chemical, and biological properties.
Micro testing is conducted to detect and quantify microorganisms prese...
Reducing manpower can be achieved through automation, streamlining processes, and outsourcing.
Implement automation for repetitive tasks
Streamline processes to eliminate inefficiencies
Consider outsourcing non-core functions
Cross-train employees to handle multiple roles
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posted on 20 May 2024
I applied via Naukri.com and was interviewed in Apr 2024. There were 2 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
posted on 23 Mar 2022
I applied via Recruitment Consulltant and was interviewed in Feb 2022. There were 2 interview rounds.
posted on 5 Sep 2021
I applied via Recruitment Consultant and was interviewed in Aug 2021. There was 1 interview round.
I applied via Referral and was interviewed in May 2021. There were 5 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
Cqa and cpp are critical quality attributes and critical process parameters respectively used in oral manufacturing.
Cqa refers to the physical, chemical, biological, or microbiological property or characteristic that should be within an appropriate limit, range, or distribution to ensure the desired product quality.
Cpp refers to the process parameter that must be maintained within a narrow range to ensure the desired p...
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