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Resmed

Cloud-connected medical devices and software platforms

MLR Content Library Specialist

Data ManagementConfirmed live in the last 24 hours
Full-timeBengaluru, Karnataka, IndiaNo salary listed

About the Job

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 digital asset management 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 digital asset management, customer relationship management, and project management platforms such as Asana.
  • Ability to track and interpret workflow and content performance metrics.
  • Ability to support US-region stakeholders and work a shift aligned to US time zones (3:00 PM–12:00 AM IST).
  • Deep understanding of how claims, references, and compliance requirements translate into structured, reusable content systems.
  • Ability to design and manage scalable metadata frameworks that enable automation, searchability, and workflow efficiency.
  • Hands-on experience with MLR/digital asset management platforms and a strong understanding of workflows, approvals, and integrations within regulated environments.

Responsibilities

  • 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 digital asset management, project management tools such as Asana, customer relationship management 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.

About the Company

Resmed

Cloud-connected medical devices and software platforms

ResMed creates cloud-connected medical devices and software platforms to treat and manage sleep apnea, COPD, and other chronic diseases. Its devices (like sleep therapy gear) collect patient data and deliver therapy, while connected software platforms enable remote monitoring, coaching, and caregiver support. The company sells medical devices and offers software subscriptions, generating revenue from product sales and ongoing service fees. Unlike some competitors, ResMed combines hardware with cloud-based analytics and a broad ecosystem that supports patients, healthcare professionals, and caregivers across more than 120 countries. Its goal is to improve patient care and quality of life while reducing hospital visits and overall healthcare costs.

Company size
5,001-10,000
Company stage
IPO
Headquarters
San Diego, CA
Founded
1989

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