IPQA Interview Question Quiz 1 Posted on August 7, 2023August 7, 2023 By Shiv Kumar 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 Uncategorized