Reltio Developer

Cloudxtreme; Kolkata District, Chennai District, Bengaluru; On-site; INR 800,000 - 1,200,000; Full time

Job summary

Cloudxtreme is seeking a qualified MDM specialist to develop and maintain Reltio-based master data management solutions for clean, unified pharmaceutical data across systems.

You will configure match/merge rules, survivorship, and data models, and integrate Reltio with ERP, CRM, and Clinical platforms while enforcing data quality and regulatory compliance.

The role requires hands-on experience with Reltio MDM and pharma data domains, with collaboration alongside analysts and data stewards.

Qualifications

• 2+ years of hands-on experience with Reltio MDM platform.
• Experience with pharmaceutical data domains (e.g., Product, HCP, HCO, Clinical Trial data).
• Strong knowledge of REST APIs, JSON, Reltio Console, and Reltio Integration Hub.

Responsibilities

• Develop and configure Reltio MDM components including match/merge rules, survivorship, workflows, and data models.
• Integrate Reltio with upstream/downstream systems (e.g., ERP, CRM, Clinical platforms).
• Implement data quality rules and cleansing logic specific to pharmaceutical data (e.g., product codes, regulatory identifiers).
• Support data migration and onboarding activities from legacy systems.
• Collaborate with business analysts and data stewards to refine requirements.

Skills

Reltio MDM

REST APIs

JSON

Reltio Console

Reltio Integration Hub

Data governance

Regulatory compliance

GxP

21 CFR Part 11

Job description

Role Summary:

Responsible for developing, and maintaining Reltio-based MDM solutions to support clean, unified person and product data across pharmaceutical systems.

Key Responsibilities:

• Develop and configure Reltio MDM components including match/merge rules, survivorship, workflows, and data models.


• Integrate Reltio with upstream/downstream systems (e.g., ERP, CRM, Clinical platforms).


• Implement data quality rules and cleansing logic specific to pharmaceutical data (e.g., product codes, regulatory identifiers).


• Support data migration and onboarding activities from legacy systems.


• Collaborate with business analysts and data stewards to refine requirements.

Required Experience:

• 2+ years of hands-on experience with Reltio MDM platform.


• Experience with pharmaceutical data domains (e.g., Product, HCP, HCO, Clinical Trial data).

Required Skills:

• Strong knowledge of REST APIs, JSON, Reltio Console, and Reltio Integration Hub.


• Familiarity with data governance and compliance standards (e.g., GxP, 21 CFR Part 11).