DataOps Engineer job opportunity at AstraZeneca.

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DateMore Than 30 Days Ago bot
AstraZeneca DataOps Engineer
Experience: 5-years
Pattern: full-time
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degreeAssociate
loacation Mexico - Guadalajara, Mexico
loacation Mexico - Guada..........Mexico

AstraZeneca is currently looking for an IT DataOps Engineer to join our R&D IT Solution Delivery Team to manage and maintain our SaaMa product, which is GxP compliant, part of Clinical Development Platforms, and used across late-stage science teams in all therapeutic areas. You will be part of our BizDevOps team and will be responsible for working cross-functionally with other team members such as the Product Lead, DevOps Lead, and technical engineers. Key Responsibilities The role of our ideal candidate will include, but is not limited to: Build, Test, Deploy, and Release : Follow standard SDLC and ITIL processes using Agile methodology to deliver fixes and enhancements Application Management : Work on application enhancements and upgrades when necessary, and be open to tackling challenging tasks/requirements Ticket Ownership : Take ownership of assigned L2/L3 level tickets/tasks and drive them to closure Troubleshooting : Troubleshoot application issues by reviewing application logs and performing dry runs of application code. Identify issues and provide fixes through application code changes if necessary Issue Resolution : Provide resolutions for user-reported issues within defined timelines (as per internal SLA/OLA standards) Proactive Monitoring : Monitor ticketing queues and other support channels proactively to quickly acknowledge and respond to user-reported issues while meeting defined response SLAs Collaboration : Liaise with other internal teams/vendors (third-party suppliers) as applicable for addressing application issues and project needs Communication : Send detailed and timely communications to users in case of planned/unplanned outages. Lead outage calls and drive them to resolution Documentation : Follow good documentation practices, including creating Knowledge Base Articles (KBAs) and publishing them for quicker and easier access Backlog Management : Create backlogs/stories/epics in JIRA (as appropriate) and work on them based on business priority Stakeholder Engagement : Excel at collaborator engagement Continuous Learning : Constantly strive to learn and upskill according to the organization's goals and demands Essential Requirements 3-5 years   of working experience with analytical and reporting tools (Crystal Reports, MicroStrategy/Business Objects (BO), or equivalent) Experience in   data engineering   and   data pipelines   is an advantage Experience working with   inbound and outbound integration   and   data Extract, Transform, and Load (ETL) Ability to work effectively as a member of multi-functional teams across programming, biostatistics, data management, and clinical sciences Knowledge of   relational databases   and experience using multiple clinical data management systems Excellent   written and verbal communication   and   relationship management   skills Experience working with   JIRA, Confluence, BitBucket Experience with   Cloud Platforms   such as   AWS   or   Azure Ability to work independently with minimum supervision Self-motivation and ability to contribute to rapidly evolving programs Nice to Have Experience with   change management processes   in GxP-validated SaaS environments Knowledge of   Agile/Scrum methodology Engineering mindset to help design and implement Clinical Data Solutions adhering to a Products on Platform delivery model Ability to manage diverse stakeholders and ensure delivery to a high degree of satisfaction Ability to work independently in a dynamic, fast-moving environment Confident communication and interpersonal skills to lead customers, from technical personnel to senior stakeholders, in urgent or critical situations Knowledge of using/creating   build tools   and   CI/CD   (Maven, Ant, SonarQube, or similar tools) Experience programming in   Java   or other   object-oriented programming languages Experience delivering or developing workshop material, training, gap analyses, or requirements gathering sessions with business and system stakeholders Big Plus if You Know EDC build (Rave)/Inform   and   global library maintenance   support experience Experience with   SaaMa/Life Science Data Hub/e-Clinical   platforms Experience working in a global organization where stakeholders and project team members are geographically dispersed Experience assisting in specialized analysis and reporting standards development activities (e.g., clinical coding, clinical dictionaries, and data analysis & reporting standards such as SDTM, ADaM, TLFs) or expertise in Biometrics functions (e.g., Programming or Statistics) Accredited certifications   from SCDM/ACDM or any vendor-offered data management training End-to-end knowledge of   clinical trial development processes   and associated system landscapes Experience implementing   IT Solutions Industry Standards   (e.g., SDTM CDISC) in either collection (CDASH) or tabulation (SDTM) Good understanding of   FDA/ICH guidelines   for clinical study data Experience working with   external vendors and CROs   to support Standards or EDC integrations with third-party platforms (Central Lab, ePRO, IRT, Data Review/Monitoring, etc.) Educational Requirements Bachelor's or Master's degree in a relevant field such as Health Sciences, Life Sciences, Data Management, Information Technology, Biostatistics, or equivalent experience. Why Join Us? Join us at a crucial stage of our journey in becoming a digital and data-led enterprise. Make the impossible possible by building partnerships and ecosystems, creating new ways of working, and driving scale and speed to deliver exponential growth. Focused and committed, and backed with the investment to succeed, we're driving cross-company change to disrupt the entire industry. So, What's Next? Are you up for an exciting challenge and ready to make a difference? If so, hit   Apply   today—we can't wait to hear from you! Date Posted 21-ene-2026 Closing Date 05-feb-2026 AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

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