Avani Consulting Looking for QUALITY-IT / Mysore

Roles and Responsibilities Purpose of Job: To support laboratory applications, GxP systems/software, and handling of IT issues. Key Responsibility Area: Experience in Pharmaceutical Industries (Quality-IT). Knowledge of computer system validation (CSV), PLC, and software-related qualification and validation activities. Familiarity with 21 CFR Part 11 and GMP guidelines. Preparation and support implementation of all IT procedures as per GMP requirements. Assist in software qualifications/verification of privileges. Experience in electronic data backup, archival and resolution, maintenance of respective IT-related logs. Experience in audit trail verification for electronic data generated in instruments (GC, HPLC, etc.). Knowledge of user management (creation/modification of User IDs and passwords, assigning privileges upon request) for laboratory and GMP software. Assist in investigations related to software issues like connectivity/communication failures, data missing, etc. Execution of hardware, network, and software installation, configuration, and maintenance/troubleshooting of desktops and laptops. Hands-on experience in troubleshooting systems, printers, and servers & configuring printers (Dot-matrix printer and Bar code). Coordinate with service engineers and vendors for software-related issues. Quickly identify and solve network-related problems (switches, crimping, and punching). Troubleshoot video conference equipment. Coordinate with Helpdesk, Server team, Network team, Field engineers, and vendors for proper follow-up until call closure. Personal Profiling: Follow instructions from the respective department Head/Designee. Self-motivator / Go-getter.

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