Unison Pharmaceuticals Walk in on 21st May 2023 for B.Pharm, M.Pharm, B.Sc, MS/M.Sc for Multiple Positions

Unison Pharmaceuticals- Walk in on 21st May 2023 for B.Pharm, M.Pharm, B.Sc, MS/M.Sc for Multiple Positions

Unison Pharmaceuticals Walk in

Qualification: B.Pharm, M.Pharm, B.Sc, MS/M.Sc
Experience : 03-07+years

Department: HPLC Analyst – Quality Control
Role: Sr. Officer / Executive
Job Location: Ahmedabad( Moraiya )

Time and Venue

21st May , 10.00 AM – 4.00 PM

Unit II, B – 3,Steel Town, Opp. CIL Nova Petro, Behind HOF, Moraiya, Taluka : Sanand, Ahmedabad 38 22 13.

Contact – Manisha Rajput ( 0797575010163 )

Unison Pharmaceuticals is urgently seeking a talented HPLC Analyst for our Quality Control team. Apply now to become a part of our team.

Experience: 3-7 years

Job Role: HPLC Analyst – Quality Control

Designation: Sr. Officer / Executive

Location: Moraiya, Ahmedabad.

Roles and Responsibilities

1. HPLC Operation (Analyst) – Assay

Collect worksheet and sample for analysis as per plan
Check the instrument calibration details

Purging the interior part of the instrument
Take the columns as per worksheet and put in instrument
Initiate solution preparation for analysis as per worksheet which majorly includes; Mobile Phase, Standard and sample

Prepare HPLC sequence for analysis and get it review by reviewer
As per the sequence initiate the analysis and online verify SSC criteria as per worksheet
Post completion of the analysis perform documentation and send to reviewer

Calculate final analysis result as per the standard formula mentioned in worksheet and match the result with worksheet range

2. HPLC Operation (Analyst) – Dissolution

Collect worksheet and sample for analysis as per plan

Check the instrument calibration details
Purging the interior part of the instrument
Take the columns as per worksheet and put in instrument

Initiate dissolution solution preparation for analysis as per worksheet and also prepare dissolution medium
Perform dissolution analysis as per the criteria mentioned in worksheet
Post completion of the analysis perform documentation and send to reviewer

Calculate final analysis result as per the standard formula mentioned in worksheet and match the result with worksheet range

3. HPLC Operation (Analyst) – Others

RM- Assay, RS, IR

In process- Assay by UV and HPLC
PV Sample- Assay by UV and HPLC, Dissolution
FP- Assay, Dissolution, RS, DT, Average weight, hardness, Friability, IR

Cleaning validation

Perks & Benefits

Dynamic work environment

Career development opportunities
Work-life balance
Free transportation

Free insurance coverage for self, spouse, and kids
Range of learning opportunities to help employees grow and thrive

If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills, we encourage you to apply for this position.

Please submit your resume to [email protected] to be considered for this role. Join our team at Unison Pharmaceuticals and take the first step towards a rewarding career.

Post Views: 677

About the Author

By shivpharma2016

May 19, 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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