Axa Parenterals QA Executive Interview Questions and Answers

Q1. What is gmp in pharma
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Q2. What is ALCOA principle
Ans. 
ALCOA principle is a guideline for ensuring data integrity in regulated industries, emphasizing data should be attributable, legible, contemporaneous, original, and accurate.
• Attributable - Data should be traceable to its source.

• Legible - Data should be clear and easy to read.

• Contemporaneous - Data should be recorded at the time of observation.

• Original - Data should be the first recording of the information.

• Accurate - D...read more
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Q1. Previous KRA and job role
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Q1. Previous experience
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Related job roles and work culture

Q1. What is Tablet inprocess
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Q2. Need of line clearance
Ans. 
Line clearance is necessary to prevent cross-contamination and ensure product quality by verifying that the production area is clean and ready for the next batch.
• Prevents cross-contamination between different products or batches

• Verifies that the production area is clean and free of any residues

• Ensures that equipment is properly sanitized before starting a new batch

• Confirms that all materials and components are in the c
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Q3. Purpose of stability study
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Stability studies are conducted to evaluate the shelf life and storage conditions of a product.
• Stability studies help determine how long a product can be stored without significant changes in quality or efficacy.

• They are important for establishing expiration dates and storage instructions.

• Factors such as temperature, humidity, light exposure, and packaging materials are considered in stability studies.

• Results of stabil...read more
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Q4. What is validation
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Validation is the process of ensuring that a product or system meets the requirements and specifications set for it.
• Validation confirms that the product meets the customer's needs and expectations

• It involves testing the product under real-world conditions

• Validation is often done at the end of the development process to ensure the product is ready for release
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