Teva Pharmaceuticals Adl Research Associate Interview Questions and Answers

Q1. Mainly around the projects implemented and overall experience
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Q1. More about each project. Done by panel from US
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Q1. More centered around learning about the role.
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Q1. Analytical method development , Analytical method validation
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Q2. ICH Guidelines and Anvisa guidelines
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Basics of chemistry and reactions of chemistry method reeactions basic chemical structures and many things realted to the chemistry

Q1. What is oos ?and example of it
Ans. 
OOS stands for Out of Specification. It refers to test results that fall outside the specified limits.
• OOS results can indicate a potential issue with the testing process or the quality of the product.

• Examples of OOS include a drug potency test result that is lower than the specified limit or a food sample that exceeds the allowed microbial count.

• OOS results require investigation to determine the cause and may lead to p
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Q2. What is oot what is QMS
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Oot stands for out of tolerance and QMS stands for Quality Management System.
• Oot refers to a situation where a measurement or result falls outside the acceptable range of values.

• QMS is a set of policies, processes, and procedures implemented by an organization to ensure quality in its products or services.

• Examples of QMS include ISO 9001 certification and Six Sigma methodologies.
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Q1. Tell more about ur subjects u studies in semister
Ans. 
I studied subjects related to biology, chemistry, and data analysis in the semester.
• Biology: focused on genetics, cell biology, and ecology

• Chemistry: covered organic and inorganic chemistry principles

• Data analysis: learned statistical methods and data interpretation
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Q2. Tell about ur family
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I come from a close-knit family of five, including my parents, older sister, and younger brother.
• My parents have always been supportive of my education and career choices.

• My older sister is a doctor, and she inspired me to pursue a career in research.

• My younger brother is currently studying engineering and we enjoy discussing science and technology together.
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Q1. How you will start the method development?
Ans. 
To start method development, I would first review the literature, define the objectives, gather necessary materials and equipment, and plan the experimental design.
• Review the existing literature to understand the current knowledge and methods used in the field.

• Define clear objectives and research questions to guide the method development process.

• Gather all the necessary materials, reagents, and equipment required for t...read more
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Q2. What is Data integrity
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Data integrity refers to the accuracy, consistency, and reliability of data throughout its lifecycle.
• Data integrity ensures that data remains unchanged and reliable over time.

• It involves maintaining the accuracy and consistency of data during storage, processing, and transmission.

• Data integrity can be achieved through various methods such as checksums, encryption, and error detection and correction.

• Examples of data int...read more
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Q1. Technical people will ask basics and if some one unable to answer they will not go for complex questions and reject candidate. Also for panel it is important to be transparent, if you don't know any answer...read more
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Q1. Please flexible on your expectations, HR will offer according to Salary range fixed for the designation.
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