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Annora Pharma
Filter interviews by
I applied via Walk-in and was interviewed before Sep 2021. There were 2 interview rounds.
Filter shock during filtration can be caused by sudden changes in pressure or flow rate, leading to filter damage or failure.
Immediately stop the filtration process to prevent further damage to the filter
Inspect the filter for any signs of damage or clogging
Replace the filter if necessary
Investigate the root cause of the filter shock to prevent future occurrences
I applied via Walk-in and was interviewed in Jan 2021. There were 3 interview rounds.
Change control is a process that ensures all changes to a system are documented, reviewed, approved, and implemented in a controlled manner.
Change control is essential for maintaining the stability and integrity of a system.
It involves documenting and tracking all proposed changes, including their impact and risks.
Changes are reviewed and approved by a designated change control board or committee.
Proper testing and val...
Risk management is the process of identifying, assessing, and prioritizing potential risks and taking measures to minimize or mitigate their impact.
Identifying potential risks
Assessing the likelihood and impact of each risk
Prioritizing risks based on their severity
Developing strategies to minimize or mitigate risks
Implementing risk management plans
Monitoring and reviewing risks regularly
Examples: financial risk, cybers
VMP stands for Vendor Master Plan. It is a strategic document that outlines the approach and activities for managing vendors in an organization.
VMP is a comprehensive plan that includes vendor selection, evaluation, and performance management.
It defines the criteria for selecting vendors and the process for evaluating their performance.
The plan also outlines the responsibilities and roles of various stakeholders involv...
Incident is an unexpected event that may or may not have an impact on product quality, while deviation is a planned or intentional change that may affect product quality.
Incident is unplanned, while deviation is planned
Incident may or may not have an impact on product quality, while deviation may affect product quality
Incident requires investigation to determine the root cause, while deviation requires investigation to...
HPLC and GC are analytical techniques used to separate, identify, and quantify components in a mixture.
HPLC (High Performance Liquid Chromatography) is used for separating compounds in a liquid mixture based on their interaction with a stationary phase and a mobile phase.
GC (Gas Chromatography) is used for separating compounds in a gas mixture based on their partitioning between a stationary phase and a mobile phase.
Bo...
HPLC is used to determine the presence and quantity of various substances in a sample.
HPLC stands for High Performance Liquid Chromatography.
It is commonly used in pharmaceutical, environmental, and food industries.
HPLC separates and analyzes compounds in a sample based on their interactions with a stationary phase and a mobile phase.
It is a powerful tool for identifying and quantifying components in complex mixtures.
E...
posted on 11 Feb 2024
I applied via Approached by Company and was interviewed in Aug 2023. There were 3 interview rounds.
Change control is a process used to manage and document changes to a system or process.
Change control ensures that changes are properly reviewed, approved, and implemented.
It helps to minimize risks and ensure that changes do not negatively impact the quality or functionality of the system.
Change control typically involves documenting the change request, assessing its impact, obtaining necessary approvals, implementing...
Process validation is the process of establishing documented evidence that a process consistently produces a product meeting predetermined specifications.
There are three types of process validation: prospective validation, concurrent validation, and retrospective validation.
Prospective validation is conducted before the process is put into routine use.
Concurrent validation is performed during routine production.
Retrosp...
Audit trail is maintained by documenting and tracking all activities and changes made to a system or process.
Audit trail is created by recording all actions, events, and transactions that occur within a system.
It helps in ensuring accountability, traceability, and compliance with regulations.
Audit trail can be established through the use of logs, timestamps, and version control.
It is important to capture relevant infor...
Yes, I am interested in Microbiology analytical review.
I have a strong background in microbiology and enjoy analyzing data in this field.
I have experience conducting microbiological tests and interpreting the results.
I am familiar with various microbiological techniques and methodologies.
I am interested in staying updated with the latest advancements in microbiology research.
I believe that my knowledge and skills in mi...
Purified water specification refers to the set of requirements and standards that purified water must meet.
Purified water should have a low level of impurities, such as minerals, chemicals, and microorganisms.
It should meet the specifications outlined by regulatory bodies, such as the United States Pharmacopeia (USP) or European Pharmacopoeia (EP).
The pH level of purified water should be within a specific range, typica...
The purified water specification for microbial quality assurance.
Microbial specification for purified water is crucial to ensure its safety and suitability for use.
The specification typically includes limits for various microorganisms, such as bacteria, fungi, and endotoxins.
Commonly used tests for microbial quality assessment include total viable count, microbial identification, and endotoxin testing.
The specification...
Validation is the process of evaluating a system or component during or at the end of the development process to determine whether it satisfies specified requirements.
Functional Validation: Ensuring that the system meets the functional requirements.
Performance Validation: Verifying that the system performs as expected under different load conditions.
Security Validation: Checking the system for vulnerabilities and ensur...
I applied via Walk-in and was interviewed in Dec 2023. There was 1 interview round.
Reviews of PVR and PQRS can be conducted through a systematic process involving data analysis and evaluation.
Collect and analyze data related to PVR and PQRS
Evaluate the performance and quality based on established criteria
Identify areas of improvement and develop action plans
Implement changes and monitor the impact
Continuously review and update the process to ensure ongoing quality assurance
posted on 9 Oct 2023
I applied via Naukri.com and was interviewed before Oct 2022. There were 2 interview rounds.
posted on 29 Jun 2022
I applied via Approached by Company and was interviewed before Aug 2021. There were 3 interview rounds.
I applied via Walk-in and was interviewed in Sep 2023. There were 2 interview rounds.
based on 2 reviews
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Executive
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Junior Officer
80
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| ₹1.5 L/yr - ₹3.5 L/yr |
Officer
75
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| ₹2 L/yr - ₹5 L/yr |
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