Officer, Quality Control Lab at Amneal India

, , India -

Full Time

Start Date

Immediate

Expiry Date

14 Oct, 26

Salary

0.0

Posted On

16 Jul, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Control, Analytical Testing, GMP, GDP, ALCOA, Dissolution Testing, UV-Vis Spectroscopy, IR Spectroscopy, Stability Testing, Regulatory Compliance, EHS Compliance, Laboratory Monitoring

Industry

Pharmaceutical Manufacturing

Description

Description: This role is responsible for conducting in-process and final product quality analyses and inspections within a quality control laboratory 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 laboratory 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 laboratory 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 sand stability quality analyses and inspections within the QC laboratory in compliance with regulatory and internal standards. * To operate Instrument like Dissolution, UV and IR-Instruments. * To perform the testing as per ALCOA * Identify ongoing quality issues and recommend preventive measures to avoid potential production problems * Maintain accurate and complete documentation of all laboratory testing activities in accordance with GDP and GMP requirements Additional Responsibilities: * Comply with all applicable EHS policies, SOPs, statutory requirements, and use the prescribed PPE while performing assigned duties. * Identify and promptly report unsafe acts, unsafe conditions, near misses, incidents, and environmental hazards, and support corrective and preventive actions. * Actively participate in EHS training, emergency preparedness, risk assessment, and continuous improvement initiatives to promote a safe, healthy, and environmentally responsible workplace.

Responsibilities

Responsible for conducting in-process and final product quality analyses and inspections within a pharmaceutical QC laboratory. The role involves operating analytical instruments and ensuring all testing complies with GMP and regulatory standards.