Senior Technical Writer - Quality Control Support

Role: Technical Writer specializing in QC documentation at Novo Nordisk's Clayton site, supporting aseptic production processes. Responsibilities: design, improve, and maintain processes for API, IFP, and OFP QC document creation, revision, and change control; ensure document compliance, clarity, and user-friendliness; collaborate cross-functionally with stakeholders; coach and mentor other writers; support standardization projects and document governance groups; manage project timelines and metrics. Requirements: Bachelor's degree or equivalent; minimum five years' experience in technical writing within engineering, life sciences, or related fields; strong understanding of GMP and process documentation; proficient in language, document control, and tools; experience in process improvement methodologies (LEAN preferred); strong planning, organization, and change management skills; effective communicator. High-Value: expertise in operational QC documentation, GMP compliance, cross-functional collaboration, process improvement, and project management within biopharma manufacturing. WorkSetup: primarily on-site at Clayton with up to 10% travel; office environment.