Senior Specialist, IT Validation Services
Hyderabad, INPosted Jul 9, 2026
Career Areas Career Stories Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Careers Home Life at BMS Career Areas Student Opportunities Events How We Recruit Career Stories Search this site Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Single PositionView All JobsSenior Specialist, IT Validation ServicesHyderabad - TS - IN No longer accepting applications.Job IDR1604221Date posted07/06/2026DepartmentNot ApplicableSenior Specialist, IT Validation ServicesSr. Specialist Computer System Validation (CSV) efforts for systems and applications in the pharmaceutical GxP space.Collaborate with cross functional and multi-location IT Delivery teams, business users and IT Quality staff to ensure that CSV activities are planned and executed in accordance with internal procedures. Work with one-up manager and peers to propose effective and efficient quality strategies.Evaluate, propose, and implement technology solutions that improve digitization, compliance, and productivity. Serve as a CSV subject-matter-expert in support of internal and external regulatory inspections. Collaborate with peers across BMS on procedures relating to quality and computer system validation.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 TechnicalParticipate in CSV activities for applications across multiple GxP business areas to ensure 'fit for use' before release to production environmentParticipate in Qualification activities as it relates to infrastructure applications and hardware in a timely mannerBe part of the team that Conducts risk & impact assessments to determine the extent of validation and qualification requirementsImplementation of organizational IT controls in accordance with applicable regulations and internal proceduresAuthor CSV deliverables including but not limited to Plans & Summary ReportsSupport the SLC process as it relates to application validation and infrastructure qualificationIdentifies opportunities for simplification, automation for CSV activities and partners with IT Delivery teams and IT Quality to implementSupports inspections and audits (internal and external).Conducts periodic reviews to ensure applications remain in a state of complianceParticipates and represents IT Validation Services in problem management and audit remediation activitiesProvides regular status updates to one up manager and escalates any potential issues in a timely mannerSupport CSV staff across defined GxP business unit applications to ensure 'fit for use' before release to production environmentQualifications & ExperienceB.E./B.Tech. or equivalent in computer science, engineering, life science fieldA minimum of 7-9 years of experience in computer systems validation in the pharmaceutical industry, including at least 3 years managing CSV projectsExperience validating one or more of the following systems (desirable): CTMS,...