Officer Quality Control Testing

Amneal Pharmaceuticals; India; On-site; INR 500,000 - 700,000; Full time

Job summary

Amneal Pharmaceuticals in India is seeking a quality analyst responsible for in-process and final product quality analyses and inspections in a GMP/GDP framework. You will interpret results, operate testing devices, and maintain documentation to ensure product integrity.

The role supports CAPA activities and continuous improvement within 21 CFR/ICH-aligned regulatory standards, contributing to product quality across manufacturing operations in India.

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 specifications
• Operate measuring devices and testing equipment according to predefined methods to accept or reject products
• Test random samples of finished goods to verify conformance with quality standards
• Report manufacturing process deviations and defects in finished goods to stakeholders
• Identify ongoing quality issues and recommend preventive measures
• Maintain accurate documentation of testing activities per GDP/GMP requirements
• Support corrective and preventive actions arising from quality investigations

Job description

Job Description:

Description:

This 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 interprets and evaluates analytical results in terms of accuracy and precision against predefined specifications to ensure product integrity. Various measuring devices, testing equipment, and predetermined methods are employed to accept or reject products based on prescribed specifications. The role 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 are identified, documented, and reported in accordance with Good Manufacturing Practices. Random samples of finished goods are tested to verify conformance with internal and regulatory quality standards. The position supports continuous improvement initiatives by suggesting enhancements to testing methods and quality processes. It operates within a structured quality management framework aligned with 21 CFR Part 210 and 211, ICH guidelines, and applicable Indian and international pharmaceutical regulations.

Essential Functions:

• 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, testing equipment, and follow predetermined methods to accept or reject products
• 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