Reltio Developer (Associate Data Management) at Amgen · Hyderabad

Reltio Developer (Associate Data Management) Location: India - Hyderabad Career Category Engineering Job Description ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. About the Role We are seeking a skilled Reltio MDM Developer with 2–5 years of experience in Master Data Management (MDM) to join us as Associate, Data Management who will design, develop, and implement scalable MDM solutions on the Reltio platform. The ideal candidate will have strong expertise in Reltio configuration/Integration Hub, Lifecycle Actions (LCA), Java-based development, and API integrations, along with domain experience in Pharma/Life Sciences. Key Responsibilities Design and implement Reltio MDM solutions, including data models, entities, relationships, and hierarchies Configure L3 Configuration, Entity Data Modeling and develop Lifecycle Actions (LCA) for event-driven data processing and business workflows Develop Java-based custom logic/services to support Reltio integrations and extensions Implement and manage match/merge rules and survivorship strategies for golden record creation Build and maintain real-time and batch integrations using REST APIs, messaging, and file-based approaches Work with Reltio Integration Hub (RIH) or equivalent frameworks for data ingestion and distribution Configure and manage crosswalks, reference data, and group attributes Develop and enforce data quality rules, validation, and enrichment processes Collaborate with data engineering, analytics, and business teams for seamless data consumption Support data governance and stewardship workflows, including DCR lifecycle Ensure data lineage, traceability, and compliance across MDM processes Troubleshoot and optimize performance of Reltio implementations Basic Qualifications Bachelor’s degree with 2–4 years of experience in IT, Engineering, or related field (or equivalent experience) Must-Have Skills Strong hands-on experience with Reltio MDM platform Deep expertise in Lifecycle Actions (LCA) development and event handling in Reltio Strong programming skills in Java (for custom logic, APIs, and integrations) Proficiency in SQL (advanced querying, data validation, performance tuning) Good experience in Python for data processing and automation Strong experience in API integrations (REST/SOAP) and microservices architecture Expertise in: Match/Merge and survivorship rules Data modeling (entities, relationships, hierarchies) Crosswalks, reference data, and golden record concepts Experience with batch and real-time data integration patterns Hands-on experience with Unix/Linux environments Strong domain experience in Pharma/Life Sciences, including: HCP/HCO mastering Affiliations Product Master / Material Master Good-to-Have Skills (Bonus) Experience with PySpark, Databricks, and large-scale data processing Experience with AWS cloud services (S3, Lambda, Glue, etc.) Experience with PostgreSQL or similar databases Exposure to GenAI / AI-driven data use cases Experience with Reltio Integration Hub (RIH) Knowledge of data visualization tools (Tableau, Power BI) Familiarity with Agile tools (JIRA, Confluence) Professional Certifications (Preferred) Reltio MDM Certification AWS / Cloud Certifications Data Engineering / SQL Certifications Soft Skills Strong analytical and problem-solving skills Excellent communication with technical and business stakeholders Ability to work in global, cross-functional teams Strong ownership and accountability Preferred Experience Experience in at least 2 end-to-end Reltio MDM implementations Experience in regulated Pharma/Life Sciences environments Exposure to enterprise-scale MDM transformations EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Role GCF: 03 Ready to Apply for the Job? We highly recommend utilizing Workday's robust Career Profile feature to complete the application process. A link to update your profile is available when you click Apply. You can then complete your Workday profile in minutes with the “Upload My Experience” functionality to upload an updated copy of your resume or you can simply edit the individual sections of your Career Profile. Please note that you should be in your current position for at least 18 months before applying to internal positions. Staff must notify their current manager if invited for an interview. In addition, Staff are ineligible to apply for open positions if (a) their performance is currently being managed on a performance improvement plan (PIP) or other locally utilized formal coaching document or (b) their most recent performance rating was not a “Partially Meets Expectations” or higher. Please visit our Internal Transfer Guidelines for more detailed information GCF Level GCF Level 03 Position Type Full time .