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ResMed is seeking a MLR Content Library Specialist to steward the claims, content, and metadata ecosystem within the MLR platform. You will ensure promotional materials are governed, reusable, and compliant, enabling scalable content operations across global markets.
The role blends content governance, data stewardship, and platform operations, requiring collaboration with Medical, Legal, Regulatory, and Marketing stakeholders.
Let’s talk about the team The MLR Content Library Specialist sits within the Marketing Operations / MarTech function and plays a critical role in enabling compliant, scalable content operations. This team is driving the transformation of content review and approval processes through platforms such as Aprimo, integrated with DAM, CRM, and project management tools. The team’s mission is to improve speed-to-market while maintaining the highest standards of regulatory compliance and content quality. The role works closely with Medical, Legal, Regulatory (MLR), Brand, Creative, Digital, MarTech, and IT teams across global and regional markets.
The MLR Content Library Specialist is the custodian of the claims, content, and metadata ecosystem within the MLR platform (e.g., Aprimo). This role is responsible for ensuring that promotional content is governed, reusable, searchable, and compliant by design through the use of structured claims, validated references, and standardized taxonomies. This is a hybrid role combining content governance, data stewardship, and platform operations.
You are detail-oriented and thrive at the intersection of content, compliance, and systems. You understand that well-structured data and governed content are key to scaling marketing operations in regulated environments. You are comfortable collaborating with Medical, Legal, Regulatory, and Marketing stakeholders while also working with platform configuration, metadata models, and process optimization. You bring a proactive mindset focused on improving workflows and reducing friction in content creation and review.
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. Comfortable supporting US-region stakeholders and working a shift aligned to US time zones (3:00 PM - 12:00 AM IST).
Joining us is more than saying “yes” to making the world a healthier place. It’s discovering a career that’s challenging, supportive and inspiring. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates.
Resmed (NYSE:RMD, ASX: RMD) creates life-changing health technologies that people love. We’re relentlessly committed to pioneering innovative technology to empower millions of people in more than 140 countries to live happier, healthier lives. Our AI-powered digital health solutions, cloud-connected devices and intelligent software make home healthcare more personalized, accessible and effective. Ultimately, Resmed envisions a world where every person can achieve their full potential through better sleep and breathing, with care delivered in their own home. Learn more about how we’re redefining sleep health at Resmed.com and follow @Resmed.