Sanofi Analytical Intern Interview Questions and Answers

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
Ans. 
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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Q1. About your self location environment
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Q1. Type of Equipment Equipment cleaning contamination batch changing tipys of document data integrity ICH Q7 safety
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Q2. Type of equipment cleaning
Ans. 
Equipment cleaning involves thorough disinfection and sterilization to prevent contamination.
• Use appropriate cleaning agents and disinfectants recommended for the specific equipment

• Follow manufacturer's instructions for cleaning and maintenance

• Regularly inspect equipment for any signs of wear or damage

• Implement proper storage practices to prevent contamination

• Train staff on proper cleaning procedures and protocols
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Q3. Batch charging process
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Q4. Tipe of contamination
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Contamination can be classified into three main types: chemical, biological, and physical.
• Chemical contamination involves the presence of harmful chemicals in a substance or environment.

• Biological contamination refers to the presence of harmful microorganisms such as bacteria, viruses, or fungi.

• Physical contamination occurs when foreign objects like glass, metal, or plastic are present in a substance.
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Q1. What is gmp and ngmp
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GMP stands for Good Manufacturing Practice, which ensures products are consistently produced and controlled according to quality standards. NGMP is not a recognized term in this context.
• GMP is a set of guidelines for ensuring the quality and safety of products during manufacturing.

• GMP covers aspects such as personnel, premises, equipment, documentation, production, quality control, and more.

• Examples of industries that ...read more
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Q2. Solvent boiling point
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Q1. Safety related , cleaning process , batch processing , as per sop and master control record some these are work in sap system
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Q2. Please introduce in yourself
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Q3. What are you known that sparkler aperation
Ans. 
I am known for my ability to inspire and motivate others to achieve their goals.
• I have a natural talent for identifying people's strengths and helping them to develop those strengths.

• I am a skilled communicator and can effectively convey my ideas and vision to others.

• I have a positive attitude and am able to maintain a sense of optimism even in challenging situations.

• I lead by example and am always willing to roll up m...read more
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Q4. What are batch charging processing
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Batch charging processing refers to the process of charging multiple items at once.
• Batch charging processing is commonly used in industries such as manufacturing and logistics.

• It involves charging multiple items simultaneously, which can save time and increase efficiency.

• Examples of batch charging processing include charging multiple electric vehicles at a charging station or charging multiple batteries in a warehouse.

• ...read more
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Q5. Do you know capa process , validation deviation process
Ans. 
Yes, I am familiar with CAPA process and validation deviation process.
• CAPA (Corrective and Preventive Action) process is a quality management system used to identify, investigate, and resolve quality issues.

• Validation deviation process is used to document and investigate any deviations from the validated process or procedure.

• Both processes are important in ensuring quality and compliance in various industries, includin...read more
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