Alembic Pharmaceuticals – Walk-In Interviews for Production / Packing on 18th June 2023 @Haridwar

Walk-In Drive at Haridwar
for our injectable Formulation site at Karakhadi – Vadodara, GUJARAT
We are inviting you to join a Great Place to Work!

Sr. Executive/Executive/Jr. Executive/Technical Officer-Production (Injectable)
Criteria:
M. Pharm/B. Pharm/Diploma/ITI
• 1 to 10 years of experience
Exposure to aseptic practices and good documentation practices are must
Job Role:
• Handle manufacturing skids, Fedegari autoclaves, Isolator, lyophilizers, vial washing and tunnel, vial/ ophthalmic /PFS filling and aseptic filtration, FFS, CIP/SIP, filters, microsphere refiner, active freeze drying System.
• Execute manufacturing activities as per SOP.
Operation, cleaning, sterilization, qualification and maintenance of solution preparation systems.

Sr. Executive/Executive/Jr. Executive/Technical Officer-Packing (Injectable)
Criteria:
• M. Pharm/B. Pharm/Diploma/ITI
• 1 to 10 years of experience
•
Exposure to aseptic practices and good documentation practices are must
Job Role:
• Handle labelling machine: Brothers & Ambica Pharma, autocartoning machine- IMA PG, Blister Packing Machine- IMA PG, Track & Trace – Utopia, Automatic Leak testing Machine- Bonfiglioli, Wilco.
• Ensure operation, cleaning, qualifications and maintenance of manual visual inspection.
• Prepare and update documents like SOPs, BMRS, Protocols and master documents of production
CITY-HARIDWAR

Sunday, 18 June 2023
9:30 AM to 3:30PM

Venue
Hotel Hyphen Pentagon Mall, Plot No. C1, Sector -12, SIDCUL, Haridwar, UTTARAKHAND

Freshers may not attend this Walk-In-Interview, please send your CV to [email protected]
Those who are unable to attend the Walk-In may send their updated resume with the details of total experience, current CTC, expected CTC & notice period on [email protected]
Please note that Alembic Pharmaceuticals Limited does not hire consultants/agents who promise interviews/jobs for monetary consideration/registration fees. Beware of such fraudulent calls.
www.alembicpharmaceuticals.com

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About the Author

By shivpharma2016

June 17, 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 72%

Alembic Pharmaceuticals – Walk-In Interviews for Production / Packing on 18th June 2023 @Haridwar