Honour Lab Interview Questions, Process, and Tips

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
Answered by AI
Add your answer
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
Answered by AI
Add your answer
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
Answered by AI
Add your answer

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
Answered by AI
Add your answer
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
Answered by AI
Add your answer
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.
Answered by AI
Add your answer

Scientific question and development Novel Process.

Q1. Based on our daily work, handling chemicals reagents like that
Add your answer
Q2. Our job responsibility, subject orriented, analytical data etc
Add your answer

About safety management

Q1. Chromatography, principle, mobile phase ,stationary phase
Add your answer

A aptitude plus coding test consisting of multiple c questions and basic mathematics question

Q1. Basic questions about data, python,sql. A case study type question
Add your answer
Q2. What is the lifecycle of data
Ans. 
The lifecycle of data refers to the stages of data from its creation to its disposal.
• Data creation

• Data storage

• Data processing and analysis

• Data sharing and dissemination

• Data archiving and disposal
Answered by AI
Add your answer