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I appeared for an interview in Jan 2017.
I am a dedicated and detail-oriented research associate with a strong background in data analysis and project management.
Completed a Master's degree in Biology with a focus on genetics
Experience conducting research projects and analyzing data using statistical software
Managed multiple research studies simultaneously and presented findings at conferences
Skilled in literature review and writing scientific reports
I appeared for an interview in Jan 2017.
Seeking new challenges and opportunities for growth.
Looking for new challenges and opportunities to learn and grow professionally.
Interested in expanding my skill set and gaining new experiences.
Seeking a more supportive work environment or better work-life balance.
Want to explore different research areas or industries.
Current job lacks opportunities for advancement or development.
Top trending discussions
I appeared for an interview in Nov 2020.
P2P cycle refers to the process of procuring goods or services from a supplier and making payments for them.
The cycle starts with identifying the need for goods or services.
The next step is to create a purchase order (PO) and send it to the supplier.
The supplier then delivers the goods or services and sends an invoice to the buyer.
The buyer verifies the invoice and matches it with the PO and goods received.
If everythin...
I appeared for an interview in May 2017.
posted on 19 Dec 2019
I applied via Referral and was interviewed before Dec 2018. There were 3 interview rounds.
The Ich limit for methanol is 0.6% and it is classified as a class 3 solvent.
The Ich limit for methanol refers to the maximum allowable amount of methanol in a pharmaceutical product.
The Ich limit for methanol is set at 0.6%, meaning that the concentration of methanol should not exceed 0.6% in the product.
Methanol is classified as a class 3 solvent according to the International Council for Harmonisation of Technical R...
The specification limit for known and unknown impurities varies depending on the specific substance being tested.
The specification limit for known impurities is typically set by regulatory agencies or pharmacopoeias.
For example, the United States Pharmacopeia (USP) sets limits for known impurities in pharmaceutical substances.
The specification limit for unknown impurities is usually determined through method validation...
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 applied via Referral and was interviewed in May 2022. There were 3 interview rounds.
I applied via Approached by Company and was interviewed in Dec 2022. There were 3 interview rounds.
I applied via Referral and was interviewed in Feb 2024. There were 2 interview rounds.
Change is required to adapt to evolving market trends, improve efficiency, and stay competitive.
Adapt to evolving market trends to meet customer demands
Improve efficiency by implementing new technologies or processes
Stay competitive by staying ahead of competitors and offering innovative solutions
I appeared for an interview before Apr 2024, where I was asked the following questions.
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