Neuland Laboratories AGM Interview Questions and Answers

Q1. Tablets scoreline test guideline
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Q1. Experience on previous work, company
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Q1. Related to work profile and experience eqipment handling, documentation, leadership
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Q1. Salary nigotiation and other formalities
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Q1. Process Validation related.
Ans. Description of process validation and impact
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Q2. CPP parameters description and impact on which CQA
Ans. 
CPP parameters refer to Critical Process Parameters which have a significant impact on Critical Quality Attributes (CQA) in manufacturing processes.
• CPP parameters are specific process variables that must be controlled within a certain range to ensure product quality.

• Examples of CPP parameters include temperature, pressure, flow rate, and mixing speed.

• The impact of CPP parameters on CQA can be seen in the final product ...read more
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Q3. Stability studies for pharmaceutical products.
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Q4. Annual report submission procedure for usfda approved products.
Ans. 
The annual report submission procedure for USFDA approved products involves compiling data on product performance, safety, and compliance with regulations.
• Compile data on product performance, safety, and compliance with USFDA regulations

• Submit the annual report to the USFDA within the specified deadline

• Include information on any changes in manufacturing processes or product labeling

• Ensure all data submitted is accurate
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Q1. Reason for leaving the job
Ans. For better opportunity and diversity in my career.
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Q1. Regarding my PhD work and industrial work
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Q1. Sallery and relocation
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Q1. How to recovered amount calculated in accuracy parameter validations
Ans. 
Recovered amount in accuracy parameter validations is calculated by comparing the actual amount with the expected amount.
• Calculate the difference between the actual amount and the expected amount

• Verify if the recovered amount falls within an acceptable range of error

• Adjust the recovered amount based on any discrepancies found

• Document the process and findings for future reference
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Q1. What is qualification of m/c in packing. Tell me flow process, which way u did qualification in your previous company.
Ans. 
Qualification of machine in packing and flow process
• Qualification of machine in packing involves testing and validating the machine's performance and capabilities

• Flow process includes steps like installation, operational testing, performance testing, and documentation

• In my previous company, we followed a qualification protocol that included IQ, OQ, and PQ stages

• We also conducted periodic requalification to ensure the m
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Q2. What is OEE, SHIFT WISE SHOW ME OEE CALCULATIONS.
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Q1. How r u doing the change part validation & its process. What is action plan if leak test failed in blisters.
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Q1. Why u want to leave the company. What is your CTC & etc.
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Aptitude written test containing 30 questions.

Q1. About the previous work experience
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Q2. About scale up and technology transfer
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