Kwality Pharmaceuticals Ltd. has announced a new recruitment drive for experienced pharmaceutical professionals in the Quality Department. The company is inviting applications from candidates with hands-on HPLC (High-Performance Liquid Chromatography) experience for multiple Quality positions. This is an excellent opportunity for professionals looking to build a career in a reputed pharmaceutical manufacturing company operating under cGMP and regulatory standards.

Interested candidates meeting the eligibility criteria can send their updated CV to the official HR email mentioned below.

Organization Details

Particular Details

Company Name

Kwality Pharmaceuticals Ltd.

Department

Quality Department

Job Type

Full-Time

Industry

Pharmaceutical Manufacturing

Job Location

1-A Industrial Area, Nurpur, Raja Ka Bagh, Himachal Pradesh – 176201

Experience Required

1–6 Years

Mandatory Skill

Hands-on experience in HPLC (High-Performance Liquid Chromatography)

Available Positions

Kwality Pharmaceuticals Ltd. is hiring for the following roles:

Officer – Quality

Senior Officer – Quality

Executive – Quality

Eligibility Criteria

Candidates should possess:

Experience in the pharmaceutical industry.

Hands-on experience in HPLC operation and analysis.

Knowledge of HPLC troubleshooting and instrument maintenance.

Strong understanding of cGMP, GLP, and regulatory guidelines.

Excellent analytical, documentation, and communication skills.

Key Responsibilities

Selected candidates may be responsible for:

Performing HPLC analysis of raw materials, finished products, and stability samples.

Operating, calibrating, and maintaining HPLC instruments.

Preparing analytical reports and maintaining laboratory documentation.

Investigating laboratory deviations and Out of Specification (OOS) results.

Ensuring compliance with cGMP, GLP, SOPs, and regulatory requirements.

Supporting method validation, method transfer, and laboratory audits.

Maintaining data integrity in laboratory records.

Required Technical Skills

Candidates should have knowledge of:

HPLC Instrument Operation

Chromatographic Data Analysis

Method Validation

Method Transfer

cGMP & GLP Compliance

Laboratory Documentation

Instrument Calibration

OOS/OOT Investigation

Regulatory Guidelines

Analytical Troubleshooting

Why Join Kwality Pharmaceuticals Ltd.?

Opportunity to work with a reputed pharmaceutical manufacturer.

Exposure to advanced analytical laboratory equipment.

Professional career growth in Quality Control.

Learning opportunities under experienced professionals.

Work environment focused on quality, innovation, and compliance.

How to Apply

Interested candidates can share their updated CV through the official email below:

Email: hrd.hp@kwalitypharma.com

Contact Number: +91 91498 05912

Job Location

Kwality Pharmaceuticals Ltd.

1-A Industrial Area, Nurpur, Raja Ka Bagh, Himachal Pradesh – 176201

Frequently Asked Questions (Technical FAQs)

1. What is HPLC and why is it important in pharmaceutical quality control?

HPLC (High-Performance Liquid Chromatography) is an analytical technique used to identify, separate, and quantify compounds in pharmaceutical products. It ensures product quality, purity, potency, and regulatory compliance.

2. Which regulatory guidelines should HPLC professionals be familiar with?

Candidates should have knowledge of cGMP, GLP, ICH guidelines, pharmacopoeias (IP, USP, BP), ALCOA+ data integrity principles, and applicable regulatory requirements.

3. What common HPLC troubleshooting skills are expected?

Professionals should be able to resolve issues such as high system pressure, peak tailing, baseline noise, retention time shifts, poor resolution, detector errors, and pump or injector problems.

4. What documentation is required in a pharmaceutical quality laboratory?

Analysts must maintain analytical worksheets, chromatograms, calibration records, logbooks, SOP compliance records, investigation reports, and electronic data in accordance with data integrity requirements.

5. What are the career opportunities after gaining HPLC experience?

Professionals with HPLC expertise can progress to Senior Executive, Assistant Manager, Quality Control Manager, Analytical Development Scientist, Laboratory Manager, Validation Specialist, or Regulatory Affairs roles.