Honour Lab Interview Questions and Answers

Q1. What is GMP and cGMP
Ans. 
GMP stands for Good Manufacturing Practices and cGMP stands for current Good Manufacturing Practices.
• GMP is a set of guidelines that ensure products are consistently produced and controlled according to quality standards.

• cGMP is an updated version of GMP that incorporates current best practices and technologies.

• Both GMP and cGMP are crucial in industries like pharmaceuticals, food, and cosmetics to ensure product safet...read more
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Q2. What is batch procedure
Ans. 
Batch procedure is a method of processing data or tasks in groups or batches rather than individually.
• Batch procedure involves grouping similar tasks together to be executed at the same time.

• It helps in optimizing resources and improving efficiency by reducing processing time.

• Examples include batch processing in computer systems, where multiple jobs are executed together, and batch production in manufacturing, where pr...read more
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Q3. What is validation
Ans. 
Validation is the process of ensuring that a product, service, or system meets the requirements and specifications set forth.
• Validation involves checking if the product meets the customer's requirements.

• It ensures that the product is fit for its intended use.

• Validation can include testing, inspection, and review processes.

• Examples of validation include software testing to ensure it functions correctly and validation of...read more
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Q1. Introduces you’re self
Ans. 
I am a dedicated EHS professional with 5 years of experience in implementing safety programs and ensuring compliance with regulations.
• Bachelor's degree in Environmental Health and Safety

• Certified Safety Professional (CSP) certification

• Experience conducting safety audits and inspections

• Implemented training programs on hazard communication and PPE

• Strong knowledge of OSHA regulations
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Q2. Your experience on audit handling briefly
Ans. 
Handled audits by conducting thorough inspections, documenting findings, and implementing corrective actions.
• Conducted regular audits to ensure compliance with EHS regulations

• Documented audit findings and communicated them to relevant stakeholders

• Implemented corrective actions to address any non-compliance issues

• Maintained audit records for future reference
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Q3. Have you work on iso documentation
Ans. 
Yes, I have experience working on ISO documentation.
• I have worked on developing and implementing ISO 14001 Environmental Management System documentation.

• I have experience in maintaining ISO 45001 Occupational Health and Safety Management System documentation.

• I have conducted internal audits to ensure compliance with ISO standards.

• I have updated ISO documentation based on changes in regulations or company policies.
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Scientific question and development Novel Process.

Q1. Based on our daily work, handling chemicals reagents like that
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Q2. Our job responsibility, subject orriented, analytical data etc
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About safety management

Q1. Chromatography, principle, mobile phase ,stationary phase
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