Bisleri International Pvt. Ltd – Walk-In Interviews for Quality Executive on 13th

Bisleri International Pvt. Ltd – Walk-In Interviews for Quality Executive on 13th – 14th Feb’ 2023

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Bisleri is the leading brand in the bottled water industry. We are the pioneers, having a nationwide network for manufacturing, sales, and distribution.

Walk in – Quality Executive – Bangalore

Preferable Only Male Candidates
Qualification: B.Sc Chemistry / M.Sc(Science) in Organic Chemistry, Bio-Chemistry, Microbiology, Chemistry
Experience: 1-3 yrs

Job Location: Bangalore

Roles and Responsibilities :

Maintain the sanitary and hygienic condition of the Manufacturing line to achieve required results

Monitor Water quality testing (Raw and Product water) as per Bisleri and BIS requirements,
responsible for Maintaining the Outside laboratory sending the Raw and Finished product water, containers, closures testing etc. as Per Bisleri/BIS protocol.
Checking and approval of Labels, closures, preforms, Jars etc.

As and When required has to visit Co-packer manufacturing facility, Inspection and updating the quality system.
New Vendor development etc.
Customer Complaints handling, Market/Customer visit, RCA (Root cause analysis) and CAPA (Corrective and preventive action Report) preparation. Etc.

Analysis of Chemical parameters as per BIS / Bisleri requirements (IS 14543:2016)
Maintain the GMP/GHK of the processing line
Maintaining and reviewing of the all related records on day to day basis.

Maintain Product Shelf Life Samples availability as per BIS/Bisleri norms.
Incoming RM/PM Analysis.
Online Quality Checks, Online Process control, Package appearance of the Product, etc..

Daily Calibration of the Instrument like pH meter, TDS meter, Turbidity meter, Thermometer etc and reporting accordingly
Preparation of the solution, reagents and standardization of the solution etc..
Market survey collection of samples and analyzing and reporting

Maintaining the Date coding of both primary and secondary packages.
Maintain product hold and release system
Customer complaint handling

Prepare the syrup as per schedule within the time frame
Follow up the syrup testing schedule and maintain the specification as per norms.
Do the calibration of online measuring devices and instruments

LOCAL LANGUAGUE IS MANDATORY: Kannada, English, Hindi

Benefits: PF, ESI, Insurance, ONROLL Job

Walk-In Date: 13th February – 14th February, 2023

Time: 10.30 AM – 4.00 PM

Venue: Sy. No-51, shanumangala village, ramanagara taluk and district Bidadi-562109

Post Views: 562

About the Author

By shivpharma2016

February 13, 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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