Officer, Quality Control Lab
Amneal Pharmaceuticals India · Remote
Source and collection record
Last observed by our collector: . This is not a manual review or a confirmation from the employer.
Employer requisition: 8331
Job type and experience labels are automated discovery categories. The employer determines eligibility. Original experience wording was not retained separately; check the current employer page.
Your application evidence checklist
Mark the statements you can support after reading the employer source. This checklist stays on this page; it does not score your eligibility or submit an application.
0 of 3 checks marked. Keep unresolved requirements as questions for the employer.
Collected role description
The candidate should have minimum 2-3 year's experience in same funciton 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.
Collected minimum qualification
Education: B. Pharm - Required M. Pharm - Preferred 2 year or more in 2-6 years Specialized Knowledge: Licenses:
Collected experience requirement
2-6 years