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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...
I applied via Referral and was interviewed in Feb 2021. There were 3 interview rounds.
Problems during tablet manufacturing and equipment/process qualification/validation.
Common problems during tablet manufacturing include issues with tablet compression, coating, and packaging.
Equipment and process qualification/validation is necessary to ensure consistent quality and compliance with regulations.
Examples of equipment validation include calibration of instruments and testing of equipment performance.
Proce...
Change control & deviation are critical aspects of project management. Proper handling ensures project success.
Establish a change control board to review and approve changes
Document all changes and deviations
Assess the impact of changes on project scope, schedule, and budget
Communicate changes to all stakeholders
Implement changes only after approval
Monitor and control changes to ensure they do not negatively impact the...
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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...
I applied via Approached by Company and was interviewed before Jun 2021. There were 2 interview rounds.
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 applied via Recruitment Consulltant and was interviewed before Jul 2023. There were 3 interview rounds.
I use a variety of tools such as project management software, communication tools, and data analysis tools to effectively manage tasks and teams.
Project management software (e.g. Trello, Asana)
Communication tools (e.g. Slack, Microsoft Teams)
Data analysis tools (e.g. Excel, Google Analytics)
I applied via Walk-in and was interviewed before Aug 2023. There were 2 interview rounds.
Through investigation case
I have high expectations for the Assistant Manager position and am seeking a change to further develop my leadership skills and contribute to a dynamic team.
Seeking new challenges and opportunities for growth
Desire to take on more responsibilities and lead a team
Passion for driving results and making a positive impact
Looking to apply previous experience and skills in a new environment
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