Description The position is responsible for in-process and final product quality analyses and inspection in compliance with established specifications, standards, and regulatory requirements. The role involves interpreting and evaluating analytical results for accuracy and precision using approved methods, calibrated instruments, and defined procedures. The role tests random samples of finished goods, audits and monitors manufacturing processes and outputs against internal and regulatory standards, and identifies ongoing quality issues to prevent potential production risks.

The position supports accept/reject decisions, reports manufacturing process deviations and defects, maintains robust documentation, and contributes to continuous improvement in product quality and compliance.

Essential Functions - Perform In-Process Testing (IPT) and Finished Product (FP) Testing as per approved specifications
Interpret and evaluate analytical results for accuracy, precision, and compliance
Execute Sampling and Testing Procedures for RM/PM (Raw Material / Packaging Material)
Review and approve Certificate of Analysis (COA) Documentation
Conduct Review of Analytical Data (RM/PM/FG/IP/IV) and ensure data integrity




Identify quality issues and support Change Control & Deviation Management
Review and investigate Out-of-Specification (OOS) and OOT (Out of Trend) results
Ensure compliance with 21 CFR Part 210 & 211 (Code of Federal Regulations – Current Positive Manufacturing Practice for Drugs)
Maintain Positive Documentation Practices (GDP) and laboratory records
Support Internal and External Audits and regulatory inspections
Use analytical instruments and measuring devices for accept/reject decisions
Report manufacturing deviations, defects, and improvement recommendations Additional Responsibilities - To be responsible for Investigation related to LIR, deviations, OOS and OOT.
To be responsible for Initiation of Deviations, OOS, OOAL, CRN and CAPA's.
To be responsible for Handling of Caliber e-LIMS
Activities other than defined in the Job responsibility are to be done as per the requirement of HOD, by following HOD's instruction and guidance.

Education QUALIFICATIONS - Bachelors Degree (BA/BS) B. Sc.
Required
Master Degree (MS/MA) M. Sc.
Preferred Experience:
3 years or more in 3 - 6 Years Specialized Knowledge: Licenses:

📌 Senior Officer, Quality Control Ahmedabad
🏢 Amneal Pharmaceuticals
📍 Ahmedabad