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Executive, Quality Control at Amneal India
, gujarat, India -
Full Time

Start Date

Immediate

Expiry Date

19 Aug, 26

Salary

0.0

Posted On

21 May, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Quality Control, Analytical Testing, GMP Compliance, In-process Inspection, Laboratory Instrumentation, Method Validation, Data Integrity, OOS/OOT Reporting, Regulatory Adherence, Product Quality Analysis

Industry

Pharmaceutical Manufacturing

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 * Review and maintain GMP documentation and analytical records   Additional Responsibilities: * Participate in method validation, verification, and transfer activities as required. * 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.
Responsibilities
Responsible for performing in-process and final product quality analyses and inspections to ensure compliance with regulatory standards. The role involves monitoring manufacturing processes, interpreting analytical results, and reporting product defects or deviations.