Quiz [catlist id=451 numberposts=50 pagination=yes] 99 Created on August 07, 2023 By shivpharma2016 IPQA Interview Question Quiz 1 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 is the primary responsibility of an IPQA officer in the pharmaceutical manufacturing process? To ensuring compliance with cGMP guidelines and approved procedures during manufacturing. To ensure that the vendor's quality management system (QMS) meets business requirements and standards For building Management For new employee recruitment 2 / 10 Question 2: Which department is responsible for conducting in-process checks and inspections in a pharmaceutical manufacturing facility? In-Process Quality Assurance (IPQA) department. Warehouse Department Engineering Department None 3 / 10 Question 3: What is the purpose of conducting line clearance before starting a new batch or product? To ensure that the production area and equipment are free from any residues or materials from the previous batch. To ensure the equipment qualification For Inventory Control For finished Product testing 4 / 10 Question 4: Which approach is used to monitor critical process parameters and identify process instability? Statistical Process Control (SPC) methods Line clearances of manufacturing activity Online Sampling Online Documentation 5 / 10 Question 5: What is the role of an IPQA officer during batch release activities? Reviewing relevant documentation to ensure the production process adhered to approved procedures and that the product meets quality standards. Planning and projection of various raw materials and consumables requirement of the department Timely complete all the Civil work of facility to ensure the all building look like new and good Reviewing relevant Cleaning validation documentation to ensure the cleaning procedure is capable to effective cleaning of equipment and facility 6 / 10 Question 6: What action should an IPQA officer take when identifying a deviation in the manufacturing process? Immediately halt the affected process and initiate a deviation report. Immediately informed to respective supervisor / In-charge to officer and above of Quality assurance department Both of the above None 7 / 10 Question 7: What does "cGMP" stand for in the pharmaceutical industry? Current Good Manufacturing Practices. Clinical Good Manufacturing Practices. Current Good Management Practices. Current Good Management Procedure. 8 / 10 Question 8: How do IPQA officers verify equipment used during the manufacturing process is properly calibrated? Reviewing calibration records to ensure compliance with the schedule. Reviewing calibration tags on instruments/equipment to ensure compliance Both of the above None 9 / 10 Question 9: Why do we calibrate an instrument at a particular interval? Because it can be possible for instruments to drift out of accuracy after qualification Because it is used in manufacturing Because it is product requirement Because it is customer requirement 10 / 10 Question 10: What is the purpose of conducting changeover verification procedures in manufacturing? To prevent cross-contamination and ensure product integrity during the transition from one product to another. To and smooth dispensing and manufacturing To easy and smooth dispensing and Packing None Your score isThe average score is 70% LinkedIn Facebook VKontakte 0% Restart quiz 33 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 isThe average score is 81% LinkedIn Facebook VKontakte 0% Restart quiz
