Kwality Pharmaceuticals Ltd has announced an excellent career opportunity for experienced pharmaceutical professionals in its Research & Development (R&D) division. The company is inviting applications for the position of Officer/Executive – Analytical Method Development & Validation (ADL) at its EU-GMP Certified manufacturing site in Amritsar, Punjab.

Candidates with 1–4 years of experience and qualifications such as B.Pharm or M.Pharm are encouraged to apply. If you are looking for a career in pharmaceutical analytical research and method validation, this opportunity offers professional growth in a regulated manufacturing environment.

Job Overview

Particular Details

Company Name

Kwality Pharmaceuticals Ltd

Industry

Pharmaceutical Manufacturing

Department

Research & Development (R&D)

Role

Analytical Method Development & Validation (ADL)

Position

Officer / Executive

Experience Required

1–4 Years

Qualification

B.Pharm / M.Pharm

Job Location

Amritsar, Punjab

Facility

EU-GMP Certified Manufacturing Site

Employment Type

Full-Time

About Kwality Pharmaceuticals Ltd

Kwality Pharmaceuticals Ltd is a well-established pharmaceutical manufacturing company with EU-GMP certified facilities. The organization focuses on quality-driven manufacturing, research, regulatory compliance, and innovation. It offers employees opportunities to work with advanced analytical instruments and global quality standards while promoting career growth and employee well-being.

Job Responsibilities

The selected candidates will be responsible for:

Analytical Method Development (AMD) for pharmaceutical products.

Method Validation as per ICH Q2(R2)/regulatory guidelines.

Method transfer and analytical troubleshooting.

Stability sample analysis and documentation.

Operation and calibration of analytical instruments.

Preparation of SOPs, protocols, validation reports, and analytical documents.

Investigation of OOS, OOT, and laboratory deviations.

Ensuring compliance with GMP, GLP, and Data Integrity requirements.

Eligibility Criteria

Applicants should possess:

Qualification: B.Pharm or M.Pharm

Experience: 1–4 years in Analytical R&D/ADL

Strong understanding of analytical chemistry and pharmaceutical testing

Knowledge of regulatory documentation and laboratory practices

Required Technical Skills

Candidates with experience in the following areas will have an advantage:

HPLC Method Development

UPLC Analysis

GC Operation

UV-Visible Spectrophotometer

Dissolution Testing

FTIR

Method Validation

Stability Studies

Data Integrity (ALCOA+)

ICH Guidelines

GMP & GLP Documentation

Analytical Troubleshooting

Why Join Kwality Pharmaceuticals?

EU-GMP certified manufacturing facility

Innovative research environment

Career growth opportunities

Employee-focused work culture

Exposure to global regulatory standards

Professional development and learning opportunities

How to Apply

Interested candidates can send their updated CV to:

Email: career@kwalitypharma.com

WhatsApp: 9639893691

Note: Verify the latest recruitment status with the company before applying.

Company Address

Kwality Pharmaceuticals Ltd

Village Nag Kalan, Majitha Road,

Amritsar – 143601, Punjab, India

Technical FAQs

1. What is Analytical Method Development (AMD) in the pharmaceutical industry?

Analytical Method Development is the process of creating reliable analytical procedures to identify, quantify, and evaluate pharmaceutical drug substances and finished products using instruments such as HPLC, UPLC, GC, and UV spectroscopy.

2. Which ICH guideline is mainly followed for analytical method validation?

Analytical method validation is performed according to ICH Q2(R2) guidelines, covering parameters such as accuracy, precision, specificity, linearity, robustness, range, and detection limits.

3. Which analytical instruments should an ADL professional be familiar with?

Candidates should have working knowledge of HPLC, UPLC, GC, UV-Visible Spectrophotometer, FTIR, Dissolution Apparatus, pH Meter, Karl Fischer Titrator, and analytical balances.

4. What documentation is important in an Analytical R&D laboratory?

Important documentation includes analytical worksheets, method development reports, validation protocols, validation reports, SOPs, stability reports, investigation reports, and compliance with ALCOA+ Data Integrity principles.

5. What are the key responsibilities during analytical method validation?

Method validation includes evaluating specificity, precision, accuracy, linearity, range, robustness, ruggedness, LOD, LOQ, and system suitability, ensuring that the analytical method consistently produces reliable and reproducible results.