Material Review Coordinator

About This Role: As a Material Review Coordinator on the GBS Material Review Team, you will play a pivotal role in streamlining the material review process at both the regional and affiliate levels. You will partner with Material Owners across various functions and regions, as well as with external agencies, to plan future material creation and reviews. By providing operational support and expertise on metadata input, you'll ensure the efficiency and accuracy of the review process. Your collaboration with Biogen’s Material Review Librarians and Veeva Vault InSCite users will aid in the creation and localization of marketing and medical materials. This role is essential in maintaining quality standards and ensuring compliance with regional and local regulations, thus directly contributing to the business's operational excellence and strategic goals. What You’ll Do: Drive the material review process at regional and affiliate levels, ensuring efficient communication for localization. Onboard and coordinate training for new team members on the materials review and localization process. Partner with Material Owners and external agencies to optimize and plan material reviews. Track key metrics and analyze data to report on the material review process through dashboards and periodic reports. Collaborate with BPO and IT Support teams to propose system enhancements and participate in User Acceptance Testing. Maintain and monitor quality of assets in Veeva Vault InSCite. Act as a point of contact for Material Owners, guiding them through creation, updates, and localization processes. Support alignment of taxonomy and metadata across company stakeholders and establish KPIs. Ensure all training materials, guidelines, and work instructions are up to date and compliant. Facilitate interactions with regional teams, ensuring efficient material review processes.

You are an organized and detail-oriented individual who thrives in a fast-paced environment. Your excellent communication skills enable you to build strong relationships across diverse teams. You possess a proactive mindset, always seeking ways to improve processes and drive efficiency. Your adaptability allows you to learn new systems quickly, and you take pride in delivering high-quality work. Your collaborative nature makes you an asset to any team, and your passion for operational excellence is evident in your work.

Bachelor’s degree or Internationally recognized qualification related to service area. Minimum of 2 years of experience in handling material review processes for a multinational pharmaceutical company or creative agency. Proficiency in using electronic tools like Veeva Vault for content management. Demonstrated familiarity with metadata standards and classifying systems. Strong computer aptitude and ability to learn systems quickly. Strong attention to detail and capability to manage multiple projects and priorities. Proficient in English; additional languages are an advantage.

Project management experience and ability to work in cross-functional teams. Previous experience in the pharmaceutical industry. Experience in Shared Services/Global Business Services delivering relevant services to an international client base. Additional Employment Conditions This role is in hybrid model of work. Please note that the role requires a candidate to be a holder of work permit & residency in Poland. #LI-Hybrid About Biogen Poland : Our Warsaw office is a complex hub for local, regional and global roles. Regardless our role and reporting line we’re driven every day by our unique purpose, working passionately to change the lives of patients affected by rare and devastating diseases. This is what gives us pride, inspires us and gives us fuel to push the boundaries of innovation. We represent over 30 nationalities and celebrate the strength that comes from differences in backgrounds, experiences, and perspectives. This commitment