Intas Pharma-Walk in for M.Pharm, B.Pharm, M.Sc in Quality, Production @Indore on 2nd July 2023

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Out of Specification & Out of Trend Investigations as per MHRA

Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world. Today, Intas is present in more than 85 countries worldwide and is growing at 20% CAGR. Around 70% of its revenues come from the international markets, particularly the highly regulated markets of EU and US. At Intas, every day and everyone works to create a world of good health, happiness and hope.

Walk-In Drive at Indore – Quality & Production (Injectable & Solid Oral) Department.

OFFICER-SENIOR OFFICER
Department : Solid Oral (Tablet Manufacturing)
Qualification : B.Pharm
Experience : 02 to 06 years • Having Experience in Granulation / Compression / Coating/Inspection.

ASSOCIATE
Department : Solid Oral (Tablet Manufacturing)
Qualification : Diploma
Experience : 02 to 06 years • Having Experience in Granulation/Compression/ Coating /Inspection

OFFICER-SENIOR OFFICER
Department : Packing (OSD & Injectable)
Qualification : B.Pharm / M.Sc. / B.Sc.
Experience : 1 to 05 years • Executing packaging activities following standard operating procedures (SOPs), ensuring compliance with regulatory guidelines and quality standards. This involves labeling, sorting, inspecting, and assembling pharmaceutical products or components.

OFFICER-SENIOR OFFICER
Department : Quality Control
Qualification : M.Sc. / B.Sc.
Experience : 2 to 05 years
• Having experience of instruments like HPLC, GC, UV, IR

SENIOR OFFICER – EXECUTIVE
Department : QA -Validation & Qualification (OSD & Injectable)
Qualification : M.Sc. / B.Pharm / M.Pharm
Experience : 3 to 07 years
• Process and Cleaning validation, protocol report and risk assessment
• Equipment qualification documents (URS, FAT, SAT, DQ, IQ, OQ, PQ) & Compliance mgt.
• SME in HVAC validation, Equipment Qualification

SENIOR OFFICER – EXECUTIVE
Department : QA – IPQA (OSD & Injectable)
Qualification : M.Sc. / B.Pharm / M.Pharm
Experience : 3 to 07 years
• Conduct in-process quality checks and monitor critical process parameters.
• Collaborate with cross-functional teams.
• Reviewand approve batch records, standard operating procedures (SOPs)

OFFICER-SENIOR OFFICER
Department : Oncology Parenteral (Manufacturing)
Qualification : B.Pharm / M.Pharm
Experience : 2 to 05 years
• Exposure to work in Bulk Manufacturing/Mfg skid with multiple vessel/NDDS area, Aseptic filling SVP, Lyophilization, Media fill, Qualification, QMS.

Job Location : Matoda Plant, Ahmedabad

Walk in Interview
Date : 2nd July, 2023, (Sunday)
Time : 10:00 am to 05:00 pm
Venue : Enrise By Sayaji Rau, Indore 27/1, 27/2, Village Pigdambar, Rau,Tehsil Mhow, Mumbai – Agra National Hwy, Indore, Madhya Pradesh 453331

HPLC Interview Questions

• Please carry your updated resume all educational, experience & salary documents
• Candidates who have appeared for an interview at Intas in the last six months are requested not to apply
• Only candidates having experience in globally regulated plants (USFDA, MHRA, etc.) should apply
• All candidates must adhere to COVID-19 guidelines during the interview process (Wearing of mask, Social Distancing, Sanitization of Hands, etc.)
• Interested candidate may share their updated resume on [email protected]

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About the Author

By shivpharma2016

June 29, 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%

Intas Pharma-Walk in for M.Pharm, B.Pharm, M.Sc in Quality, Production @Indore on 2nd July 2023

Intas Pharma-Walk in for M.Pharm, B.Pharm, M.Sc in Quality, Production @Indore on 2nd July 2023

Out of Specification & Out of Trend Investigations as per MHRA

HPLC Interview Questions

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