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Labeling Content Strategist

Job in Hudson, St. Croix County, Wisconsin, 54016, USA
Listing for: Acolad group
Full Time position
Listed on 2026-02-01
Job specializations:
  • Healthcare
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

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Acolad is the global leader in content and language solutions. Its mission is to support companies in every industry to scale across markets and enable growth through cutting-edge technology and localization expertise. Established in 1995, the group is present in 22 countries across Europe, North America and Asia, with over 1.600 employees supported by a network of +10.000 linguists around the world.
At Acolad, every position is key to our global growth: we know that we will only succeed if our people succeed.
Joining Acolad means a unique opportunity for professional development through a collaborative global environment that promotes talent and creativity. We are continuously looking for new talent (like you!) to support our mission to drive growth and innovation across some of the world’s leading brands.
Check out Our brand video to learn more about us!

About

The Role

Seeking a Labeling Content Strategist to join our Life Science US Team. This role will be responsible for overseeing the technical back-end strategy of medical device digital and print labeling content.
Help drive innovative solutions in the healthcare industry through planning and implementation of structured technical authoring system for digital and print medical device labeling deliverables, including Instructions for Use (IFU), technical manuals, help files, and GUI software strings for patients, technicians, and healthcare professionals.

Key Responsibilities
  • Lead the exploration of technical solutions development to meet client growing needs.
  • Conduct a comprehensive assessment of client labeling content ecosystems across products and platforms.
  • Collaborate with Labeling Manager and technical writer team to develop and implement complex content strategies to ensure consistent, harmonized, and compliant quality of content, considering version control and complex implementation strategies.
  • Gain cross‑functional alignment on content strategy through team collaboration and presentation of ROI data.
  • Collaborate and align with stakeholders to define labeling content and design requirements and develop a scalable Labeling Content Strategy roadmap with clear milestones and timelines.
  • Evaluate various Component‑based Content Management Systems (CCMS) and advise client on selection of a tool that supports the developed labeling content strategy, ensuring the selected solution supports governance, scalability, and long‑term business objectives.
  • Lead the technical writing team in execution of pilot implementations for New Product Development (NPD) labeling within the CCMS to validate workflows, structure, and system capabilities prior to full‑scale rollout.
  • Promote best practices for harmonization and optimization of legacy labeling content for migration into the CCMS, partnering closely with CCMS vendors and client labeling SMEs to ensure quality.
  • Create and maintain labeling content strategy documentation, including information architecture, content models, style guides, taxonomies, and glossaries to ensure structured authoring is harmonized for tone and terminology throughout digital and print deliverables.
  • Collaborate with professionalism to build consensus among stakeholders and teams.
  • Provide editorial insight into content creation process, including structured authoring optimization to support content reuse.
  • Advise Labeling Manager of best practices and importance of content governance.
  • Work closely with CCMS vendor to support schema validation and publication testing as needed to ensure compliant and high‑quality publication pipelines.
Requirements Educational background
  • Bachelor's degree with an emphasis on English, Journalism, Technical Writing, Communications, Library Science, or equivalent experience required.
Professional background
  • Experience in labeling management in the regulated medical device industry required.
  • Experience managing and implementing structured authoring, especially Mad Cap Flare, XML‑based, DITA, and Component Content Management Systems (CCMS).
  • Technical writing and labeling development experience required,…
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