i
Bal Pharma
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Process validation as per FDA approach involves establishing documented evidence that a process consistently produces a result meeting predetermined specifications.
Understand the process and its critical parameters
Develop a validation plan
Perform process qualification
Conduct process performance qualification
Document and analyze the validation data
Implement ongoing process monitoring and control
Cleaning validation is the process of ensuring that equipment used in manufacturing is properly cleaned to prevent cross-contamination.
Identify critical equipment and surfaces that require cleaning validation
Establish acceptance criteria for cleanliness
Develop a cleaning validation protocol
Perform cleaning verification tests
Analyze test results and compare against acceptance criteria
Document the cleaning validation pro
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I applied via Company Website
Pharmaceutical products in manufacturing of the product granulations packaging of the product
Raw material used in carefull
Human body system endocrine system reproductive system are all the body system related
I applied via Naukri.com and was interviewed in Mar 2022. There were 5 interview rounds.
The previous company has a rich history of over 50 years in the software industry.
The company was founded in 1969 and has been a leader in the software development market since then.
It has successfully delivered numerous high-profile projects for clients across various industries.
The company has a strong focus on quality assurance and has implemented robust QA processes.
It has a track record of consistently meeting or ...
I received positive feedback from my previous company.
Received commendations for consistently meeting quality targets
Recognized for implementing efficient QA processes
Received positive performance reviews from supervisors
Process validation is the documented evidence that a process is consistently producing a product that meets predetermined specifications and quality attributes.
Process validation is a critical component of quality assurance in manufacturing.
It involves establishing documented evidence that a process is capable of consistently producing a product that meets predetermined specifications and quality attributes.
Process val...
Guidelines for process validation include establishing process parameters, conducting process performance qualification, and ongoing monitoring.
Establish process parameters
Conduct process performance qualification
Ongoing monitoring
Document all validation activities
Ensure compliance with regulatory requirements
Consider risk management principles
Involve relevant stakeholders
Area qualifications refer to the specific skills and knowledge required for a particular job or industry.
Area qualifications are often listed in job postings and include both technical and soft skills.
Examples of area qualifications for a software developer may include proficiency in programming languages, knowledge of software development methodologies, and strong problem-solving skills.
Area qualifications may also in...
I applied via Company Website and was interviewed in Jul 2021. There were 4 interview rounds.
I applied via Recruitment Consultant and was interviewed in Jun 2020. There was 1 interview round.
I applied via Recruitment Consultant and was interviewed before Nov 2019. There were 3 interview rounds.
I applied via Walk-in and was interviewed in Jul 2019. There were 6 interview rounds.
based on 1 interview
Interview experience
Executive
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QA Executive
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