Jodas Expoim Pvt Limited- Walk-In Interview for AR&D Department on April 16th, 2023

Walk-In Interview

Department: AR&D Department
Designation: Research Associate

Qualification: B.Pharmacy, M.Pharmacy, M.Sc
Experience: 2 to 8 years only
Job Description:
- Analysis of Formulation Research Development samples. (Assay, Related Substances, Osmometer,
- UV-Visible Spectrophotometer, Water Content).
- Responsible for the analysis of the in process and Finished and Stability Samples.
- Responsible for performing the analysis of HPLC, Assay and Related Substances by HPLC, Water Content by KF.
- Responsible for online documentation of analysis done.
- Responsible for online Support for Formulation department
- Responsible for Good Laboratory Practices in Analytical Research and Development.
- Responsible for Following the Calibration Schedule of the laboratory instruments as per master plan.
  Operation & Calibration of Analytical Instruments (HPLC, Analytical micro balances & pH meter).

Candidates are requested to carry the last three months payslips, Recent increment letter. Original Certificates, Aadhar Card. Interested can send their resume to [email protected]

Sunday 16th April 2023: (9.00 AM – 12.00 PM)

INTERVIEW LOCATION: JODAS EXPOIM PVT. LTD., 3rd Floor, NSL Centrum, Plot No S-1, Sy No: 1043 & 1048, KPHB Phase-III, Kukatpally, Hyderabad-500072, India.

WORK/LOCATION: JODAS EXPOIM PVT. LTD., BiotechPark, Phase III, Karkapatla

Post Views: 538

About the Author

By shivpharma2016

April 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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