Officer Executive Quality Control

Amneal Pharmaceuticals; Ahmedabad District; On-site; INR 400,000 - 700,000; Full time

Job summary

Amneal Pharmaceuticals LLC in India is seeking a QC Analyst to perform in-process and final product quality analyses and inspections, ensuring compliance with GMP and approved specifications. The role involves interpreting results and supporting acceptance decisions.

You will operate laboratory instruments, apply validated methods, and participate in method validation, SOP updates, and continuous improvement within the QC department. 3–6 years of pharma QC experience and a BSc are preferred.

Qualifications

• 3–6 years of QC experience in pharmaceutical/biotech settings.
• Bachelor's degree in science required; Master's preferred.
• Knowledge of GMP/GLP, quality systems and documentation.

Responsibilities

• Perform in-process and final product quality analyses and inspection.
• Execute FP testing and IP/FP analytical testing.
• Interpret analytical results for accuracy, precision and compliance.
• Operate laboratory instruments and testing equipment per methods.
• Support acceptance or rejection decisions for materials and products.
• Audit and monitor manufacturing processes and quality outputs.
• Contribute to SOP updates and method validation activities.
• Report deviations and anomalies promptly to supervisor.

Skills

In-process QC

Final product testing

Analytical result interpretation

Instrument operation

GMP documentation

Quality improvement

Process auditing

Education

BSc in Science

MSc preferred

Tools

Laboratory instruments

Job description

Job Description:

Description

The position is responsible for in-process and final product quality analyses and inspection in compliance with approved standards and regulatory requirements. The role involves interpreting and evaluating analytical results for accuracy and precision against established specifications. The role uses measuring devices, testing equipment, predefined methods, operations, setups, and specifications to support acceptance or rejection of materials and products. The position identifies ongoing quality issues, prevents potential production problems, and recommends improvements. The role audits, monitors, and determines the quality of manufacturing processes and outputs, performs random testing of finished goods, and reports manufacturing process deviations and product defects, ensuring data integrity, GMP compliance, and regulatory adherence.

Essential Functions

• Perform in-process and final product quality analyses and inspection
• Execute Finished Product (FP) Testing and IP/FP Analytical Testing
• Interpret analytical results for accuracy, precision, and compliance
• Operate measuring devices, laboratory instruments, and testing equipment
• Apply approved analytical methods, operations, and specifications
• Support acceptance or rejection decisions for materials and products
• Identify ongoing quality issues and prevent production risks
• Audit and monitor manufacturing processes and quality outputs
• Conduct random sampling and testing of finished goods
• Review and maintain GMP documentation and analytical records
• Report manufacturing process deviations and product defects

Additional Responsibilities

• Participate in method validation, verification, and transfer activities as required.
• Assist in updating and reviewing SOPs, specifications, and analytical procedures.
• Contribute to continuous improvement initiatives in the QC department.
• Report any out-of-specification (OOS) or out-of-trend (OOT) results promptly to the supervisor.
• Support cross-functional departments such as QA, Production, and Regulatory Affairs as needed.

Qualifications

Education: Bachelors Degree B. Sc. - Required / Master Degree M. Sc. - Preferred

Experience: 3 - 6 Years