Viatris
10+ Avendus Interview Questions and Answers
Q1. Tell me about Forced degradation study
Forced degradation study is a process used to determine the stability of a drug substance or product under various stress conditions.
Forced degradation studies involve subjecting the drug to conditions such as heat, light, humidity, and acid/base hydrolysis to simulate potential degradation pathways.
The purpose of these studies is to identify degradation products, determine degradation pathways, and establish the stability of the drug.
Forced degradation studies help in develo...read more
Q2. Explain the problems faced in validations
Validations in executive roles can face challenges due to lack of data accuracy, timeliness, and stakeholder alignment.
Data accuracy issues can lead to incorrect decisions being made.
Timeliness of data can impact the speed at which decisions can be made.
Lack of stakeholder alignment can result in conflicting priorities and goals.
Inconsistent validation processes across departments can lead to discrepancies in data interpretation.
Q3. What are the stability conditions
Stability conditions refer to the factors that contribute to the overall stability of a system or organization.
Stability conditions can include financial stability, political stability, and social stability.
In a business context, stability conditions may involve having a strong leadership team, a solid customer base, and a diversified product line.
For a government, stability conditions could include a stable economy, effective governance, and social cohesion.
Stability conditi...read more
Q4. Tell about Data integrity
Data integrity refers to the accuracy, consistency, and reliability of data throughout its lifecycle.
Ensures data is accurate and reliable
Prevents unauthorized access or changes
Maintained through data validation and verification processes
Q5. What is APQR conclusion
APQR conclusion is the final assessment and summary of the Annual Product Quality Review.
APQR conclusion is a comprehensive evaluation of the quality of a product over the course of a year.
It includes analysis of data, trends, deviations, and any corrective actions taken.
The conclusion may recommend changes to processes, formulations, or quality control measures.
Examples of APQR conclusions could be recommendations for process improvements, changes in specifications, or conti...read more
Q6. Explain about Validation parameters
Validation parameters are criteria used to ensure data input meets specified requirements.
Validation parameters can include data type, length, format, range, and presence.
For example, a validation parameter for a phone number field may require 10 digits and no special characters.
Validation parameters help prevent errors and ensure data integrity.
They are commonly used in form fields and database entries.
Q7. How to give line clearence
Line clearance is the process of ensuring that a production line is free from any previous product or material before starting a new production run.
Ensure all equipment is clean and sanitized before starting a new production run
Verify that all materials and ingredients are correct and properly labeled
Check that all previous product residue is removed from the production line
Confirm that all necessary quality checks have been completed before starting production
Q8. AAS principle and it’s application
AAS principle refers to the three key elements of authentication, authorization, and accounting in information security.
Authentication: verifying the identity of a user or system
Authorization: granting access to specific resources based on the user's identity and permissions
Accounting: tracking and logging user activity for auditing and compliance purposes
Example: A user logging into a system with a username and password (authentication), being granted access to certain files...read more
Q9. Tell me oos flow
OOS flow refers to the out of stock flow in retail operations.
OOS flow occurs when a product is not available for purchase due to being out of stock.
It is important for retailers to manage OOS flow effectively to avoid losing sales and customer dissatisfaction.
Strategies to address OOS flow include improving inventory management, implementing automated restocking systems, and setting up alerts for low stock levels.
Q10. Explain about validation plan
A validation plan outlines the process for ensuring that a product or system meets specified requirements and standards.
Defines the objectives and scope of validation activities
Identifies the resources, responsibilities, and timelines for validation
Specifies the methods and procedures for testing and evaluating the product or system
Includes criteria for acceptance and rejection of validation results
Q11. Area of interest
My area of interest is technology and innovation.
I am always curious about the latest advancements in technology.
I enjoy exploring new gadgets and software.
I am interested in how technology can be used to solve real-world problems.
I follow tech news and attend conferences to stay up-to-date.
Examples: AI, blockchain, IoT, AR/VR, cybersecurity, etc.
Q12. Calibration of HPLC
Calibration of HPLC is a process of adjusting the settings of the High Performance Liquid Chromatography system to ensure accurate and reliable results.
Calibration involves checking and adjusting the flow rate, detector sensitivity, and column efficiency.
Regular calibration helps maintain the accuracy and precision of the HPLC system.
Calibration standards are used to verify the performance of the system.
Documentation of calibration procedures and results is essential for comp...read more
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