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V S International (VSI) – Walk-Ins for QC / QA / Production / Packing / Formulation Development / Analytical Development on 9th April’ 2023

Walk-In Interviews @ V S International

Production Officer / Sr. Officer

Roles and Responsibilities

Responsible for all Production activities at Tablet Compression, Granulation, and Coating with respect to cGMP.
Maintain Weekly and Monthly Production Planning by Checking RM/PM availability and Production Equipment feasibility
Should have knowledge of documentation exposure of cGMP.

Completion of BMR (Batch Manufacturing Record), Equipment Log Book/ Shift & all cGMP Records.
Co-Ordinating with warehouse, QA, QC & Engg. Department, to run the shift activity Smoothly.
Maintaining documentation of the BMR requisitions in process.

Maintaining good housekeeping on the shop floor.
Manpower work allocation and Training.
Exposure in Regulatory Markets like EUGMP, USFDA, MHRA, TGA etc.

Desired Candidate Profile

Minimum B. Pharma
Ready to relocate Daman location

Experience: min. 2 – 5 Years
Industries: OSD (Tablet & Capsule), Pharma

Packing Officer / Sr. Officer / Executive

Roles and Responsibilities

Responsible for handling all primary and secondary packaging activities.
To coordinate with other departments like warehouse, Engineering, QC, QA

Planning for day-to-day activity in the packing department
Able to handle regulatory audits.

Desired Candidate Profile

Education: B.Sc / M.Sc. /B. Pharm / M. Pharm
Experience: 01 to 06 Years

QA Officer / Sr. Officer / Executive

Roles and Responsibilities

Vendor Management,
APQR Activity,

QMS (Change control, Handling Market Complaints, Audit Compliance)
IPQA

Desired Candidate Profile:

Education: M.Sc. /B. Pharm / M. Pharm
Experience: 01 to 06 Years

QC Officer / Sr. Officer / Executive

Roles and Responsibilities:

FP / Stability / RM / GLP section
Should have handled independently HPLC / GC

Calibration of QC Instruments

Education: B.Sc / M.Sc. /B. Pharm / M. Pharm

Experience: 01 to 06 Years

Formulation Development Research Scientist / Associate

Roles and Responsibilities:

Project development

QBD concept,
Scale-up, Technology Transfer

Desired Candidate Profile:

Education: M. Pharm
Experience: 01 to 06 Years

Analytical Development and Research Associate

Roles and Responsibilities:

Knowledge of AMV / AMT / MMD / Analysis & Calibration
Required knowledge of HPLC / GC / UV / Auto titrator / Disso.

Knowledge of GLP activity like SPC / STP / Calibration / Reference Std / Working Std. / Training

Desired Candidate Profile:

Qualification: M.Sc. / M.Pharm

Job Location: Daman

Interested candidates, please share your Updated CV, Notice period, and Expected CTC on [email protected] or WhatsApp at 9712914477.

Walk-In Date: 9th April, 2023

Time: 9.30 AM – 5.30 PM

Venue: V S International Pvt. Ltd, Plot No 11, 17&18 Golden Industrial Estate, Dabhel Road, DAMAN DIU, Daman & Diu, India

Post Views: 689

About the Author

By shivpharma2016

April 3, 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%

V S International (VSI) – Walk-Ins for QC / QA / Production / Packing / Formulation Development / Analytical Development on 9th April’ 2023

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