Torrent Pharmaceuticals Limited-Walk in Interview for multiple position on 26 mar'2023

Torrent Pharmaceuticals Limited-Walk in Interview for multiple position on 26 mar’2023

Walk in Interview

Torrent Pharmaceuticals Limited
PHARMA
Baddi, Himachal Pradesh
Walk in Interview
Date: 26 March 2023 (Sunday) Time: 9:00 am to 4:00 pm
Interview Venue:

Torrent Pharmaceuticals Limited,
Nr. Baddi University, Village Bhud- Makhnu Majra, Tehsil Baddi, Dist Solan, Himachal Pradesh -173205.

> Department: Quality Control (Formulation)
> Designation: Executive/Technical Assistant
> Criteria: B.Pharma/ M.Sc with 2 To 7 Years of relevant experience
Skills:. Exposure of analysis for Finished Product, Stability Samples & Raw Materials
⚫ Having sound knowledge of Operation, Troubleshooting of QC Instruments & Investigation of OOS/OOT/Deviation. (e.g
HPLC, GC, UV, GCMS, LCMS, FTIR, Polarimeter, UV Spectrophotometer KF, Apparatus)
Having Knowledge of Analytical Method Validation, Verification & Method Transfer Having skill for data interpretation & troubleshooting
• Exposure of QC compliance and GLP activities.
> Department: Quality Assurance (Formulation)
> Designation: Executive/Technical Assistant
> Criteria: B.Pharma / M.Sc with 2 To 7 Years of relevant experience
Skills:
Having Knowledge of Quality Management System
⚫
(Deviations, Market Compaints, 005, OOT Risk Assessment, Product Recall, PQR and Investigations).
⚫
Having Sound Knowledge of Validation. Qualification, Documents, Self Inspection, Training, BMR BPR review, Documents Issurance, Nitrosoamine Risk Assessment and Elemental Impurities Risk Assessment.
> Department: Health Safety Environment
> Designation: Executive
> Criteria: M.Sc. Environment with 2 to 7 Years of relevant experience
Skills: ETP & STP Operation and maintenance Management of Hazards, waste Bio Medical and other waste as per legal requirements. ETP lab analysis and documentation as per GMP requirements.
• Exposure in filling various Env. Returns.
> Department: Procurement
> Designation: Executive
> Criteria: B Tech (Electrical/Mechanical/Chemical) with 2 to 7 Years of relevant experience
> Skills:
Techno-commercial negotiation and finalization of orders
• Evaluation of development of new resources form competitive advantage
Preparation of MIS reports Evaluation & finalization of AMC & Service contract
Follow up with vendors & contractors for timely delivery
Good Knowledge of SAP
> Department: Information Technology
> Designation: Executive
> Criteria: B Tech (Computer Science /IT/Electronics & Tele.) MCA 2 to 5 Years of relevant experience in the manufacturing industry Experience in Hardware & Networking Designing, Implementation, Documentation and Maintenance work.
> Skills:
Others:
• Prepare & Maintain necessary GMP-related Documents and sops. IT troubleshooting skills.
Pharma knowledge of Solid orals & Quality processes. USFDA, MHRA, ANVISA & Other regulatory exposure is preferred including ICH guidelines.
Contact Person:
Shikha Sharma & Sandeep Kapil 9805508451
[email protected]
[email protected]
Please attend an interview with your latest resume, one passport-size photograph & Latest salary slip,

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About the Author

By shivpharma2016

March 20, 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 Interview for multiple position on 26 mar’2023