Torrent Pharmaceuticals Limited-Walk in an interview for QA/QC on 30 April 2023@ Sikkim

PHARMA
Recruitment: Torrent Pharmaceuticals Limited, Sikkim
Torrent Pharma, the flagship company of Torrent Group, is ranked amongst the top pharma companies of India. It is a dominant player in the therapeutic areas of cardiovascular (CV) and central nervous system (CNS) and has achieved significant presence in gastro-intestine, diabetology, anti-infective and pain management segments. Torrent Pharma has a strong international presence spanning over 70 countries with over 1200 product registrations.
We invite talented, experienced and enthusiastic professionals to be part of our ambitious journey to achieve new heights together.

Inviting applications for various positions for Unit-I & II at 32 number middle camp as mentioned below.
We are Hiring!

: WALK-IN INTERVIEW on 30/04/2023 (Sunday) 10AM to 12 PM Note:

Candidates not having relieving/experience letters of all previous companies need not to attend interview
Department Designation
Experience
Qualification
QUALITY CONTROL
Executive /Technical Assistant
2-8 Yrs
B Pharm/M Pharm/MSc
Analysis of finished products, stability samples and RM as per method analysis.

QUALITY ASSURANCE

Executive /Technical Assistant
2-8 Yrs
B Pharm/M Pharm
Knowledge of Documentation, QMS, Deviation, Change Control, Market Complaint, OOS, OOT, Validation Qualification, IPQA, Audit Compliance.

Interview Venue
Date & Time

Torrent Pharmaceuticals Limited, Middle Camp, NH – 10, 32 No.,
Gangtok, East Sikkim
30/04/2023 & 10 AM to 12 PM
Candidates who could not attend the interview can send their CVs to
[email protected]/[email protected]
* Please attend the interview with your latest resume, photograph & photocopies of (the last 3-month salary slips, the Last 6 months’ bank statements, all educational mark sheets & certificates, Previous organization experience, and relieving letters, current company appointment letters & increment letter, PAN Card & Aadhar Card).
* Candidates have to strictly follow Covid-19 guidelines.

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About the Author

By shivpharma2016

April 29, 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%

Torrent Pharmaceuticals Limited-Walk in an interview for QA/QC on 30 April 2023@ Sikkim