IT Compliance Officer (Permanent)

IT Validation & Compliance Analyst II Department - ClinOps and Regulatory GBS Organization Novo Nordisk Global Business Services (GBS) India Ensure the systems behind life-changing therapies meet the highest standards of quality and compliance from release to retirement. As an IT Validation & Compliance Analyst II in Clinical Data Solutions GBS, you will be responsible for end-to-end validation of GxP-critical systems, ensuring sustained compliance with regulatory and company requirements throughout their lifecycle. You will play a central role in driving release activities, coordinating validation efforts, and strengthening the team's quality culture. Preparing and owning the release plan for system releases, developing implementation plans, and driving all release-related activities end-to-end Collaborating with the Line of Business, vendors, and other relevant stakeholders to ensure successful delivery of projects and compliant execution of validation activities Leading and coordinating validation activities required to support each release, ensuring appropriate documentation, traceability, and quality oversight Drafting, executing, reviewing, and approving test cases (manual and/or automated using tools such as Leapwork, TOSCA), ensuring results meet defined acceptance criteria and compliance requirements Managing incidents and deviations using platforms such as ServiceNow and Vault Quality, ensuring timely investigation support and appropriate follow-up actions Maintaining IT risk assessment documentation, O&M SOPs, and compliance documents to support ongoing audit and inspection readiness Mentoring and coaching colleagues in the validation specialty area, sharing quality-related knowledge and best practices to build capability and consistent execution standards In Research & Development, you'll be part of a unit that explores bold scientific ideas and advances them into clinical testing. We combine curiosity, AI tools, and human data to develop transformative therapies. Within Research & Development, Clinical Data Solutions GBS plays a critical role in ensuring the systems that support clinical data remain validated, compliant, and fit for purpose. You will join a team that values precision, collaboration, and continuous improvement working closely with cross-functional partners to uphold the quality standards that ultimately protect patients and enable innovation. We are looking for a detail-oriented professional who thrives in a regulated environment and takes ownership of quality outcomes. Total 6 years of industry experience, of which at least 4 years must be in software testing and at least 5 years must be hands-on experience working with pharmaceutical/GxP requirements for regulated systems and applications Strong knowledge of GxP validation principles, regulatory requirements, and lifecycle management of computerised systems Experience with test automation tools (e.g., Leapwork, TOSCA) and incident/deviation management platforms (e.g., ServiceNow, Vault Quality) A relevant degree in IT, Life Sciences, Engineering, or a related discipline For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. To submit your application, please upload your CV online (click on Apply and follow the instructions). For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. .