Kwality Pharmaceuticals Ltd, a leading EU-GMP certified pharmaceutical manufacturing company based in Amritsar, is conducting a Walk-In Interview Drive on 21 June 2026 for multiple departments. This recruitment drive offers excellent career opportunities for experienced professionals in production, quality assurance, quality control, and microbiology functions.

Candidates looking for pharmaceutical manufacturing jobs, sterile production jobs, IPQA jobs, microbiology jobs, and HPLC analyst jobs are encouraged to attend the walk-in interview.

Company Overview

Company Name: Kwality Pharmaceuticals Ltd.

Location: Amritsar, Punjab

Certification: EU-GMP Certified Manufacturing Facility

Industry: Pharmaceutical Manufacturing

Kwality Pharmaceuticals is known for its commitment to quality, regulatory compliance, and advanced pharmaceutical manufacturing technologies. The company offers growth-oriented career opportunities in sterile manufacturing, quality systems, and analytical laboratories.

Open Positions

1. Vial & Ampoule Filling and Sealing

Machine: NKP – 8 Head

Designation: Operator / Technician

2. PFS (Pre-Filled Syringe)

Machine: Radiant Industries

Designation: Operator / Technician

3. DPI Filling & Sealing

Designation: Operator / Technician

4. IPQA & QMS

Designation: Officer / Senior Officer / Executive

5. Microbiology

Designation: Officer / Senior Officer / Executive

6. HPLC & AMV

Designation: Senior Officer / Executive

Walk-In Interview Details

Particulars Details

Walk-In Date

21 June 2026

Time

09:00 AM to 05:00 PM

Venue

Hotel Royal Hillton

Address

NH-07, Shamsherpur, Paonta Sahib, District Sirmour, Himachal Pradesh

Key Highlights

EU-GMP Certified Facility

Growth-Oriented Work Environment

Quality-Driven Organization

Strong Career Development Opportunities

Professional and Collaborative Culture

Department-Wise Responsibilities

Production (Vial, Ampoule, PFS & DPI)

Operate filling and sealing equipment.

Perform line clearance and machine setup.

Monitor filling accuracy and process parameters.

Maintain production records and batch documentation.

Follow GMP and safety guidelines.

IPQA & QMS

Conduct in-process quality checks.

Monitor manufacturing compliance.

Handle deviations, CAPA, and change controls.

Review batch manufacturing records.

Support regulatory inspections and audits.

Microbiology

Environmental monitoring.

Water testing and microbial analysis.

Sterility testing.

Media preparation and validation.

Microbial limit testing.

HPLC & AMV

HPLC method execution and analysis.

Analytical method validation.

Stability sample analysis.

Data integrity compliance.

Instrument calibration and qualification.

Documents Required

Candidates should carry:

Updated Resume/CV

Passport Size Photographs

Educational Certificates

Experience Certificates

Latest Salary Slip

Government ID Proof (Aadhar/PAN)

Previous Employment Documents

Why Join Kwality Pharmaceuticals?

Kwality Pharmaceuticals provides employees with exposure to advanced pharmaceutical manufacturing technologies and international regulatory standards. Professionals can build long-term careers in sterile manufacturing, quality assurance, microbiology, and analytical sciences while working in a highly regulated environment.

Technical FAQs

1. What is the role of IPQA in pharmaceutical manufacturing?

IPQA (In-Process Quality Assurance) ensures manufacturing activities comply with GMP requirements by performing line clearance, process monitoring, batch record verification, and in-process quality checks.

2. What is HPLC and why is it important in pharma industries?

HPLC (High Performance Liquid Chromatography) is an analytical technique used for identification, quantification, purity testing, stability studies, and quality control of pharmaceutical products.

3. What are the key responsibilities of a Microbiology Officer?

A Microbiology Officer performs environmental monitoring, sterility testing, water testing, microbial limit testing, media preparation, and supports contamination control programs.

4. What is a PFS manufacturing process?

PFS (Pre-Filled Syringe) manufacturing involves filling sterile drug products into syringes under controlled aseptic conditions followed by sealing, inspection, and packaging.

5. What GMP practices should production operators follow?

Production operators must follow SOPs, maintain documentation accuracy, wear proper gowning, perform line clearance, ensure cleanliness, and comply with data integrity and regulatory requirements.

Contact Information

Kwality Pharmaceuticals Ltd.

📞 9837454653, 9056855224

📧 career@kwalitypharma.com

Interested candidates can directly attend the walk-in interview on 21 June 2026 and explore exciting career opportunities with Kwality Pharmaceuticals Ltd.