Teva Pharmaceuticals Analytical 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
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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?
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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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It's was based on vigilance

Q1. How do u manage ur work and life
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Q1. What is difference between validation and qualification
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Validation ensures that the system meets the user's needs, while qualification ensures that the system is installed and operates correctly.
• Validation confirms that the system meets the user's requirements and expectations.

• Qualification ensures that the system is installed correctly and operates within predefined specifications.

• Validation is more focused on user needs and expectations, while qualification is more focuse...read more
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Q2. What is GLP and data integrity
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GLP stands for Good Laboratory Practice, which ensures the reliability and integrity of data generated in a laboratory setting.
• GLP is a set of guidelines for conducting non-clinical safety studies on chemicals, pharmaceuticals, and other products.

• It includes requirements for the organization, personnel, facilities, equipment, and documentation of studies.

• Data integrity refers to the accuracy, completeness, and reliabil...read more
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Q1. What is HPLC and GC
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HPLC and GC are analytical techniques used in chemistry to separate and analyze compounds in a mixture.
• HPLC stands for High Performance Liquid Chromatography, which uses a liquid mobile phase to separate compounds based on their interactions with a stationary phase.

• GC stands for Gas Chromatography, which uses a gas mobile phase to separate compounds based on their volatility and interactions with a stationary phase.

• Bot...read more
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