Genpact- Mega Walk-In Drive for Freshers & Experience On 12th April 2023

Genpact (NYSE: G) is a global professional services firm focused on delivering digital transformation for our clients, putting digital and data to work to create competitive advantage. We do this by integrating lean principles, design thinking, analytics and digital technologies with our domain and industry expertise to deliver disruptive business outcomes – an approach we call Lean DigitalSM. We deliver value to our clients in two ways – through digital-led, domain-enabled solutions that drive innovation, and through intelligent operations enabled by digital that design, transform and run clients’ operations. Our approach is continually refined in one of the world’s largest digital process sandboxes, where we test and improve thousands of processes. For two decades, first as a General Electric division and since 2005 as an independent company, we have been passionately serving our clients. We generate impact for clients from the Fortune Global 500 and beyond, and employ over 77,000 people in more than 20 countries, with key offices in New York City, Palo Alto, London, and Delhi

Genpact Walk-In Drive

Department : Accounts Payable, Order to Cash, Non-Voice, Transactions, Order Management, Invoice to Cash, Record to Report

Experience: 00-05+Years
Qualification: BCom/BBA
Job Location: Jaipur

Time and Venue

12th April, 11.30 AM – 1.30 PM

Genpact : Plot No 1, Jawahar Lal Nehru Marg, Near Venkateshwara Temple, Siddharth Nagar, Sector 9, Malviya Nagar, Jaipur, Rajasthan

Job description

SubSkill Set: Accounts Payable, Order to Cash, Non-Voice, Transactions, Order Management, Invoice to Cash, Record to Report

Time: 11:30 AM to 1:30PM

Location: Plot No 1, Jawahar Lal Nehru Marg, near Venkateshwara Temple, Sector 9, Malviya Nagar, Jaipur, Rajasthan 302017

Shift– Ready to work in any shift (24*7)

Work from office only

Employee will be responsible to carry out the production at process level in an utmost efficient manner adhering to all the process level protocols

Are you the one we are looking for?

Qualifications we seek in you

Minimum qualifications
* BCom/BBA Graduate

Preferred skills

* Ready to work on stretched working hours due to volume fluctuations
* Good comprehension & e-mail writing skills
* Decision making skills required
* Ability to analyze and observe things
* Interpersonal Skills
* Excel Skills – Intermediate
* Take non scripted inbound & outbound calls
* Awareness of Microsoft office resources

Responsibilities

As part of the Mortgage services team, you will be required to:
* Ability to comprehend information/data set
* Ability to deliver work as per agreed accuracy service levels along with good efficiency
* Communication with onshore team for getting the resolutions on pending information

Post Views: 465

About the Author

By shivpharma2016

April 10, 2023

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 is

The average score is 71%

Genpact- Mega Walk-In Drive for Freshers & Experience On 12th April 2023

Genpact- Mega Walk-In Drive for Freshers & Experience On 12th April 2023

Job description

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