Executive – QA Validations

Department: Quality Assurance Qualification: B.Pharm Experience: 3+ years Industry: Sterile / Injectable Manufacturing

Role Summary: Responsible for executing and documenting validation activities related to equipment, process, cleaning, and utilities to ensure compliance with regulatory requirements.

Key Responsibilities: Process Validation: Prepare and execute process validation protocols. Review Batch Manufacturing Records during validation batches. Compile and prepare validation summary reports. Monitor critical process parameters (CPPs) and critical quality attributes (CQAs).

Required Skills: Strong understanding of sterile manufacturing processes. Knowledge of cGMP and regulatory validation expectations. Good documentation and report-writing skills. Attention to detail and analytical thinking.