SRF Gujarat -Walk-In Interview For Production/ QC/ Safety Department on 28th April 2023

Walk-In Interview

SRF
Walk-In-Interview on Dt.28th April 2023 SRF Limited, Dahej
TIME 9.00 AM TO 3.00 PM
We are, with a turnover of 12,313 crore (US$ 1.6 billion) Multi-business entity with a legacy of more than 100 years, SRF Limited is a diversified chemicals conglomerate engaged in the manufacturing of industrial and specialty intermediates. To meet our continuous growth needs, we require deserving candidates for following positions in our Chemicals Business at Dahej.
Age Limit
Junior Engineer / Technician – Production
Diploma in Chemical Engineering / M. Sc / B. Sc / ITI AOCP
4-8 Years of experience in Batch Chemical Plant
Candidate must have hands on experience of Distillation Column, Multiple Reactors handling, Trouble shooting, knowledge of various pumps & valves and other field activity, work permit system etc.
(Minimum 2 Years DCS exposure is must for Junior Engineer)
Below 32 Year.
Junior Officer – Quality Control (Polymer Lab)
Qualification CIPET Diploma (DPT+industrial experience/BSC+PPT+ industrial exp./MSc.Polymer science) Diploma in Polymer Characterisation / B.Sc.+ Polymer Testing or Exp. In PTFE testing. 3-8 years of experience in Fluoropolymers, Polymers, Resins, Masterbatch, Polymer compounding, Plastic Industry, Plastic processing etc.
Experience
Age Limit
Operation of Polymer lab Instruments. Hands on experience on Plastic Testing instruments & PTFE testing’s will be added advantage.
Testing of Mechanical/Thermal/ property of polymer Below 32 Year
Junior Officer – Safety
Qualification Diploma in Chemical Engineering / M. Sc / B. Sc with ADIS / PDIS 3-8 Years of experience in Hazardous chemical Plant only
Experience
Age Limit
Candidate should have experience in green/brown field Project in of Chemical/
petrochemical industry, should experience in daily Finding Unsafe act/ Condition and Near miss reporting, should have knowledge of Form 9,10,11. Candidate should have knowledge of all types of work Permits,
Below 32 Year.
Interested candidates can walk for interview on below venue and also send their resume mentioning Job Title to mail id. SENDCV.DAHEJ@srf.com.
Venue: Hotel Shalimar, Station Road, Bharuch

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About the Author

By shivpharma2016

April 27, 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%

SRF Gujarat -Walk-In Interview For Production/ QC/ Safety Department on 28th April 2023

SRF Gujarat -Walk-In Interview For Production/ QC/ Safety Department on 28th April 2023

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