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Tata Consultancy Services(TCS) Walk In For Freshers On 30th May & 01st June 2023

Tata Consultancy Services Released Job Openings On 29/05/2023.Tata Consultancy Services is an Indian multinational information technology services and consulting company with its headquarters in Mumbai. It is a part of the Tata Group and operates in 150 locations across 46 countries..Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Tata Consultancy Services Recruitment 2023 are provided below. Interested and eligible candidates can submit application along with resume.

Vacancy Details:

Tata Consultancy Services Recruiting BA, BBA, BBM, B.Com, B.Sc, BCA and MBA Graduates with 00 years experience for Citizen Service Executive position.

Important Details :

Location : Varanasi/Benaras, Bareilly, Gorakhpur
Details of Salary: 50,000-2.5 Lacs P.A.

Time And Venue: 30 May – 1st June , 11:00 AM – 04:00 PM

Bareilly: Radha Krishna Tower, CC – 146/A, Plot No.317/1 kha, Jagatpur Lala Begum, Pilibhit Bypass Road , Bareilly , Uttar Pradesh

Job Description/Skills Required

We are looking for young and smart non-technical graduates and Post graduates for a mega e-governance project.

Please note that this job is not related to Finance/HR domain.
This is not a technical requirement hence candidates from technical background need not to apply (ex: BE, B. Tech, MCA, M. Tech & M. Sc candidates need not to apply).
Please check the below requirement & eligibility criteria

1. Required Qualification – BA, BBA, BBM, B.Com, B.Sc, BCA and MBA
2. Decent communication and interpersonal skills
3. Good personality and customer handling skills

4. Proficient in English and Local language
5. Computer savvy and good keyboard skills with accuracy
6. Full time courses only can be considered.

7. Freshers preferred
8. Operational role
9. Age – 21 – 25 Yrs

10. Not more than 2 years gap during education or employment in total
Candidates who have attended TCS interview in the last 6 months need not apply.

Post Views: 694

About the Author

By shivpharma2016

May 30, 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%

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