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Viatris

4.2
based on 3k Reviews
Proud winner of ABECA 2024 - AmbitionBox Employee Choice Awards
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10+ Avendus Interview Questions and Answers

Updated 13 Dec 2024
Popular Designations

Q1. Tell me about Forced degradation study

Ans.

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

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Q2. Explain the problems faced in validations

Ans.

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.

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Q3. What are the stability conditions

Ans.

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

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Q4. Tell about Data integrity

Ans.

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

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Q5. What is APQR conclusion

Ans.

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

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Q6. Explain about Validation parameters

Ans.

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.

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Q7. How to give line clearence

Ans.

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

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Q8. AAS principle and it’s application

Ans.

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

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Q9. Tell me oos flow

Ans.

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.

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Q10. Explain about validation plan

Ans.

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

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Q11. Area of interest

Ans.

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.

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Q12. Calibration of HPLC

Ans.

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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More about working at Viatris

Top Rated Large Company - 2024
Top Rated Pharma Company - 2024
HQ - Canonsburg, Pennsylvania, United States (USA)
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