MLR Content Library Specialist
ResMed · Bengaluru
- Experience2–5 yrs
- SalaryNot disclosed
- Work modeonsite
- Levelmid
- Posted17 Sept 2026
About ResMed
ResMed is hiring in Bengaluru in healthcare. This role looks for around 2+ years of experience.
Skills
- MLR
- regulatory review
- content compliance
- claims and references management
- content lifecycle and approval workflows
- metadata and taxonomy design
- Aprimo
- Veeva
- Adobe Workfront
- MarTech
- DAM
- CRM
- Asana
The role
An MLR content library specialist at a healthcare products company manages claims and references management, metadata and taxonomy design, and content lifecycle and approval workflows. The role aligns Aprimo, Asana, and regulated content governance across medical, legal, regulatory, and marketing stakeholders.
Full job description
ResMed is hiring for the role of MLR Content Library Specialist
Responsibilities of the Candidate :
Own and manage the centralized claims and messaging library, ensuring all claims are validated, tagged, and traceable to approved references.
Maintain one-to-many relationships between claims and variations to ensure consistency across assets.
Enable reuse of pre-approved claims to reduce unnecessary re-review cycles.
Define and maintain metadata frameworks, including region, product, content type, and approval status.
Ensure assets and claims are properly tagged to support searchability, filtering, and workflow automation.
Standardize taxonomy across global and regional teams.
Manage citation libraries and reference linking to ensure every claim is supported by approved, traceable sources.
Maintain version control and auditability of references and claims.
Support regional validation and compliance requirements.
Maintain the central repository of approved content as the single source of truth.
Manage content expiration, archiving, and re-approval triggers.
Ensure proper versioning, change tracking, and audit trails.
Partner with MLR teams to ensure workflows are configured with appropriate claims, metadata, and approval logic.
Support submission quality control before content enters review.
Drive adoption of best practices for content reuse and structured submissions.
Collaborate with MarTech and IT teams to align MLR platforms with DAM (Aprimo), project management tools such as Asana, CRM platforms, and downstream activation systems.
Ensure data consistency and synchronization across systems
Track metrics including claims reuse rate, content approval cycle time, and compliance issues related to claims and references.
Identify opportunities to improve efficiency, reduce redundancy, and strengthen governance practices.
Requirements :
Experience in MLR, regulatory review, or content compliance processes, preferably within healthcare, pharmaceutical, or other regulated industries.
Hands-on experience with MLR platforms or DAM systems such as Aprimo, Veeva, or Adobe Workfront.
Strong understanding of: Claims and references management, Content lifecycle and approval workflows and Metadata and taxonomy design
Experience working with cross-functional stakeholders across Medical, Legal, Regulatory, and Marketing functions.
Familiarity with MarTech ecosystem integrations, including DAM, CRM, and project management platforms such as Asana.
Analytical mindset with the ability to track and interpret workflow and content performance metrics.