Medley Pharmaceuticals Research Associate Interview Questions and Answers

Q1. What is gmp and ngmp
Ans. 
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. Introduction About different Development studies Information on projects handle
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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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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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It's was based on vigilance

Q1. How do u manage ur work and life
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