IPQA Interview Question Quiz 2

Created on August 07, 2023 By

Shiv Kumar

IPQA Interview Question Quiz 2

In Process Quality Assurance, IPQA is very important in any manufacturing of pharmaceutical Industries, primary role is to ensure that the manufacturing process adheres to cGMP guidelines and follows the approved standard operating procedures. also, review batch records and documentation to ensure accuracy and completeness. The Main Objective of IPQA is to maintain product quality and ensure that all finished products meet the required specifications

1 / 10

Question 1: What type of documentation does an IPQA officer review to ensure accuracy and completeness of BMR?

Batch records and IPQA reports.

Production Planing

Good receipt Note

None

2 / 10

Question 2: What does an IPQA officer do when a manufacturing process is out of control?

Take immediate action to bring the process back under control and within predefined specifications.

Take immediate action to bring inform security

Immediate inform to engineering

None

3 / 10

Question 3: How does an IPQA officer stay updated on the latest industry regulations and guidelines?

Attending industry seminars, workshops, and subscribing to regulatory agencies' newsletters.

Reading the current regulatory Guidelines updates

Attending GMPs Training

All of the above

4 / 10

Question 4: What is the purpose of conducting risk assessments in IPQA activities?

To identify and prioritize potential risks to product quality.

To make simplify production planning

For better Inventory Control

None

5 / 10

Question 5: What is the primary goal of IPQA activities during the manufacturing process?

Ensuring product quality and compliance with regulations.

Production Planning and Target Completion

Transport Validation

None

6 / 10

Question 6: What are the consequences of non-compliance with cGMP guidelines during manufacturing?

Potential product recalls, regulatory actions, and impact on patient safety.

Production Planning and Target Achievement

Finished Product Dispatch to Market

None

7 / 10

Question 7: What is the purpose of conducting routine inspections on the manufacturing floor?

To verify that each step of the manufacturing process is executed correctly.

To identify the Gaps between the actual vs written approved Procedures.

To compliance with specification and written approved Procedures.

All of the above

8 / 10

Question 8: How does an QA officer handle deviations and non-conformances in the manufacturing process?

Investigate the root cause, initiate a deviation report, and implement corrective and preventive actions.

Review, evaluation and login

analyze the risk and evaluate impact of deviation in consultation with HOD of responsible department

All of the above

9 / 10

Question 9 : What are In process checks?

Checks carried out during an activity to monitor

To ensure that the product conforms to its specification

Both of the above

Production Target Completion

10 / 10

Question 10 : Which class of Area is Required for Tablets and Capsule Manufacturing?

Class D

Class B

Class A

Class C

Your score is

The average score is 82%

0%

IPQA Interview Question Quiz 2

IPQA Interview Question Quiz 1

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