Torque Pharmaceuticals Pvt. Ltd., one of India’s well-established pharmaceutical manufacturing companies, has announced exciting career opportunities for fresh graduates in its Quality Control (QC) Department. This recruitment drive is aimed at enthusiastic and dedicated candidates who are looking to build a strong foundation in the pharmaceutical industry.

The company is inviting applications from B.Pharm and B.Sc. (Chemistry) graduates who are eager to begin their professional journey in a regulated pharmaceutical environment. The selected candidates will have the opportunity to gain hands-on experience in quality testing, analytical techniques, laboratory operations, and GMP-compliant processes.

Job Overview

Company: Torque Pharmaceuticals Pvt. Ltd.

Department: Quality Control (QC)

Qualification: B.Pharm / B.Sc. (Chemistry)

Experience: Freshers Eligible

Location: Derabassi, Punjab

Key Responsibilities

Perform routine quality control analysis of raw materials, intermediates, and finished products.

Follow Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).

Maintain laboratory records and documentation accurately.

Assist in analytical method execution and validation activities.

Support investigations related to out-of-specification (OOS) results.

Ensure compliance with regulatory and company quality standards.

Employee Benefits

Torque Pharmaceuticals offers a supportive work environment with several employee-friendly facilities, including:

Canteen Facilities

Transportation Facilities

Company Uniform

Professional Growth Opportunities

Positive Work Environment

Industry Exposure and Learning Opportunities

Why Join Torque Pharmaceuticals?

Starting a career in Quality Control provides valuable exposure to pharmaceutical manufacturing and analytical operations. Freshers joining Torque Pharmaceuticals can gain practical experience with laboratory instruments, quality systems, documentation practices, and regulatory requirements, helping them build a successful long-term career in the pharmaceutical sector.

Interested candidates can apply by sending their updated resumes to:

Email: desh.raj@torquepharma.com

Technical FAQs

1. What is the primary role of a Quality Control (QC) department in pharmaceutical manufacturing?

The QC department ensures that raw materials, in-process samples, and finished products meet predefined quality specifications before release. It helps maintain product safety, efficacy, and regulatory compliance.

2. Which analytical instruments are commonly used in pharmaceutical QC laboratories?

Common instruments include:

HPLC (High-Performance Liquid Chromatography)

UV-Visible Spectrophotometer

Gas Chromatography (GC)

Dissolution Test Apparatus

FTIR Spectrometer

Analytical Balances

3. What is the difference between Quality Assurance (QA) and Quality Control (QC)?

Quality Assurance (QA) focuses on systems, procedures, and compliance, while Quality Control (QC) focuses on testing and verifying product quality through laboratory analysis.

4. What does OOS (Out of Specification) mean in pharmaceutical QC?

An OOS result occurs when a test result falls outside the approved specification limits. Such results require a detailed investigation to determine the root cause and ensure product quality.

5. Why are GMP and GLP important in a QC laboratory?

Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) ensure consistency, reliability, traceability, and regulatory compliance in pharmaceutical testing and manufacturing activities, ultimately protecting patient safety.