I was an experienced candidate. So I was asked about the work in industry (manpower handling, guidelines, acceptance criteria for different validation, calculation of machine data etc). Interview was a bit tough.

Question

Accepted Answer

I will maintain cGMP and GDP in document

And maintain quality in production

Accepted Answer

Yes in manufacturing we maintain quality and quantity as per USFDA Guidelines

Validations are use in before of the batch ...it's help full in capacity of equipment and also uniformity of drug

SCADA is the very important role in the usfda review....its show process of the temperature and dp ,inlet temperature ,out let temperature

I was an experienced candidate. So I was asked about the work in industry (manpower handling, guidelines, acceptance criteria for different validation, calculation of machine data etc). Interview was a bit tough.

Popular interview questions of Junior Executive