Amgen
Reltio Developer (Associate Data Management)
India - Hyderabad
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- Role family
- Engineering
- Seniority
- Mid level
- Country
- IN
- Work mode
- On-site / unstated
- First seen by hirly
- 28 Sept 2026
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the posting
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
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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
.
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