Amneal Pharma is inviting applications for the role of Trainee Officer, QC Testing at Ahmedabad City, Gujarat, India. This opportunity is suitable for pharmacy candidates looking to build their career in quality control testing within a pharmaceutical manufacturing environment.

The selected candidate will be involved in in-process and final product quality analyses, inspection activities, documentation, deviation reporting, and support for quality improvement initiatives in line with GMP, GDP, regulatory and internal quality standards.

Job Details

Job Description

The Trainee Officer, QC Testing role is responsible for conducting in-process and final product quality analyses and inspections in strict compliance with established standards and regulatory requirements within a global pharmaceutical manufacturing environment.

The incumbent will interpret and evaluate analytical results for accuracy and precision against predefined specifications to ensure product integrity. The role involves using various measuring devices, testing equipment, and predetermined methods to accept or reject products based on prescribed specifications.

The position also contributes to identifying ongoing quality issues and preventing potential production problems through proactive monitoring and timely escalation. Manufacturing process deviations and defects in finished goods must be identified, documented, and reported in accordance with Good Manufacturing Practices.

The role operates within a structured quality management framework aligned with 21 CFR Part 210 and 211, ICH guidelines, and applicable Indian and international pharmaceutical regulations.

Key Responsibilities

• Perform in-process and final product quality analyses and inspections in compliance with regulatory and internal standards.
• Interpret and evaluate analytical results for accuracy and precision against established specifications.
• Operate measuring devices and testing equipment, and follow predetermined methods to accept or reject products.
• Audit and monitor manufacturing processes and outputs against defined internal and regulatory quality standards.
• Test random samples of finished goods to verify conformance with quality specifications.
• Report manufacturing process deviations and defects in finished goods to relevant stakeholders.
• Identify ongoing quality issues and recommend preventive measures to avoid potential production problems.
• Maintain accurate and complete documentation of all testing activities in accordance with GDP and GMP requirements.
• Support implementation of corrective and preventive actions arising from quality investigations.
• Support continuous improvement initiatives by suggesting enhancements to testing methods and quality processes.

Qualification

• B. Pharm – Required
• M. Pharm – Preferred

Experience

Experience required: 1 year or more in 1 – 4 Years.

How to Apply

Interested candidates can review the job details and submit their application online through the official application page.