Validation Lead Sgo

Job Title SGO Validation Lead Job Grade G9B A Function Global Information Technology Sub-function Manufacturing Quality IT Manager s Job Title Head SGO IT India Skip Level Manager s Title Global Head Manufacturing Quality IT Function Head Title Global Chief Information Officer Location Halol Areas Of Responsibility At Sun Pharma we commit to helping you Create your own sunshine - by fostering an environment where you grow at every step take charge of your journey and thrive in a supportive community Are You Ready to Create Your Own Sunshine As you enter the Sun Pharma world you ll find yourself becoming Better every day through continuous progress Exhibit self-drive as you Take charge and lead with confidence Additionally demonstrate a collaborative spirit knowing that we Thrive together and support each other s journeys Job Summary The job holder will be responsible for managing the Plant GxP Application Inventory and serving as the Technical Owner for Computer System Validation CSV documentation related to GxP applications They will oversee periodic CSV and QMS activities throughout the system lifecycle from implementation to retirement Additionally they will support the business during internal and external audits by explaining processes and documentation related to CSV and remediation Responsibilities To manage Inventory of GxP Applications for Manufacturing Quality IT Planning and review of validation deliverables for CSV Projects Preparation reviews and Approval of CSV documents as Technical Owner Ensuring the compliance of GSOP s SOP s related to Computer System Validation documentation and regulatory requirements during execution of CSV Project Understanding the working and usage of Systems such as Trackwise Validator and EDMS Compliances to IT policies and procedures regulatory requirements and support for the internal and external audits and remediation Vendor coordination and support during Installation qualification IQ Operational qualification Performance qualification PQ Identify the continuous improvement opportunities for CSV projects Documentation and control for management of CSV documents w r t IT Timely completion of validation activities with zero timeline extensions Full audit readiness with complete and compliant documentation Effective and timely closure of all related QMS records deviations CAPA change controls etc Travel Estimate Based on the need job holder can travel to other sites Job Scope Internal Interactions within the organization System Owners from site Quality Manufacturing and CQIT Corporate IT External Interactions outside the organization Business Users External Vendors Geographical Scope Provide onsite support to the site other site whenever needed Remotely Financial Accountability cost revenue with exclusive authority NA Job Requirements Educational Qualification BE B Tech MCA BCA MSc IT BSc IT Graduation PGDCA Specific Certification NA Skills Computer System Validation Understanding of IT regulatory requirements Execution of Validation Qualification activities Experience 8-10 Years in IT activities preferably in Pharma Manufacturing Your Success Matters to Us At Sun Pharma your success and well-being are our top priorities We provide robust benefits and opportunities to foster personal and professional growth Join us at Sun Pharma where every day is an opportunity to grow collaborate and make a lasting impact Let s create a brighter future together Disclaimer The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification It is not designed to contain or be interpreted as a comprehensive inventory of all duties responsibilities and qualifications required of employees as assigned to this job Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent s