Specialist II IT Validation Services

Position Summary Supports the execution of Computer Systems Validation (CSV) activities for systems and applications in Pharma GxP space under the guidance of Validation Lead/ Manager. Collaborate with peers across BMS on CSV activities. At BMS, digital innovation and Information Technology are central to our vision of transforming patients lives through science. To accelerate our ability to serve patients around the world, we must unleash the power of technology.? We are committed to being at the forefront of transforming the way medicine is made and delivered by harnessing the power of computer and data science, artificial intelligence, and other technologies to promote scientific discovery, faster decision making, and enhanced patient care.? ? If you want an exciting and rewarding career that is meaningful, consider joining our diverse team! Key Responsibilities Functional and Technical Support execution of CSV activities for applications across multiple GxP business areas to ensure 'fit for use' before release to production environment Support execution of Qualification activities as it relates to infrastructure applications and hardware in a timely manner Support validation lead in conducting risk & impact assessment to determine the extent of validation and qualification Author CSV deliverables including but not limited to Plans & Summary Reports Support the SDLC process as it relates to application validation and infrastructure qualification Review and approve change tickets for applications and ensure alignment with change management process. Conducts periodic reviews of applications to ensure applications remain in a state of compliance. Provides regular status updates to one up manager and escalates any potential issues in a timely manner Qualifications & Experience Minimum Bachelors degree and 2-4 years of experience in IT Quality, Computer System Validation and/or related field. Experience supporting validation of one or more of the following systems (desirable): SAP, ServiceNow, Veeva, Regulatory Submission systems Experience in change management process General knowledge (desirable) of IT applications, IT infrastructure, architecture of computer systems including cloud as well as networks, operating systems, databases, and software tools Good knowledge (mandatory) of IT testing practices and methodologies in the Pharma GxP space-and good working knowledge of test management tools like ALM etc. Familiarity with test automation tools desirable Understanding (desirable) of Electronic Records and Electronic Signature regulations, Data Integrity principles, GAMP and Agile methodologies Works predominately within established procedures Ability to work under minimal supervision Demonstrates openness to learning and developing. Takes a responsibility for their own development and growth Good English verbal and written communication skills including the ability to write clear and precise documentation

Location: hyderabad, IN

Posted Date: 6/12/2025