Canton Laboratories QC Analyst Interview Questions and Answers

Group discussion and HR department and Technically

Q1. Working experience and previous company salary
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Q1. Tell me about yourself
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Q1. Describe the APQR. OOS, Process Validation. And many more
Ans. 
APQR is a quality document that summarizes the results of an annual product quality review.
• APQR stands for Annual Product Quality Review.

• It is a quality document required by regulatory authorities.

• APQR summarizes the results of an annual review of product quality.

• It includes data on manufacturing processes, analytical results, complaints, deviations, and other quality-related information.

• APQR helps identify trends, pot...read more
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Q1. About your self tell me something
Ans. 
I am a dedicated and experienced professional with a strong background in law enforcement.
• I have served as a police officer for 10 years, gaining valuable experience in crime prevention and investigation.

• I have received specialized training in crisis management and conflict resolution.

• I am skilled in using various law enforcement technologies and tools, such as surveillance systems and firearms.

• I have a proven track re...read more
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Q2. Why are you leave company
Ans. 
I left the company to pursue new opportunities and challenges.
• Seeking career growth and advancement

• Looking for a more challenging role

• Exploring new industries or sectors

• Relocating to a different city or country

• Company downsizing or restructuring

• Personal reasons or family commitments
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Q1. What are all the in process carried out in oral solids
Ans. 
In the process of manufacturing oral solids, various steps are carried out to ensure quality and efficacy.
• Raw material testing and selection

• Granulation or blending of active ingredients and excipients

• Compression or encapsulation of the mixture into tablets or capsules

• Coating of tablets for protection and ease of swallowing

• Packaging and labeling of the final product

• Quality control testing at different stages

• Documentatio
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Q2. What are cleaning validation process
Ans. 
Cleaning validation process ensures that cleaning procedures effectively remove residues from equipment and surfaces.
• Cleaning validation is a documented process to demonstrate that cleaning procedures are effective in removing residues.

• It involves establishing acceptance criteria, selecting appropriate sampling methods, and performing analytical testing.

• The process includes cleaning verification, which confirms that cl...read more
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Q1. What is your positive and negative
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