QA Validation (Manufacturing QA)_Injectables_Chennai

Job Description

Greetings!!! We are seeking for a QA Validation (Dy Manager/ Manager )_Injectables for a Pharma Company at Chennai Location. Job Responsibilities: Responsible to ensures the quality and compliance of injectable products through validation and qualification activities, reviewing documentation, and conducting audits, all while adhering to GMP and regulatory requirements. Key Responsibilities: Validation and Qualification: Executes and reviews qualification/re-qualification and validation activities for equipment, systems, facilities, and plant utilities. Prepares and reviews validation/qualification protocols and reports. Conducts sampling activities as per protocols, including process and cleaning validation. Ensures all equipment, systems, and processes are validated and qualified according to GMP and regulatory standards. Documentation and Review: Reviews and approves validation lifecycle documentation (e.g., URS, DQ, FAT, SAT, IQ, OQ, PQ, PV) protocols and reports. Maintains validation registers. Reviews and approves validation deviations. Ensures all documentation is complete and accurate. Quality Assurance: Conducts quality assurance audits and inspections. Identifies and addresses potential quality issues. Ensures adherence to GMP and regulatory requirements. Participates in investigations and CAPA activities. Interested Candidates Kindly share your updated cv to khyati@bvrpc.com