• Lead complex documentation projects and create high-quality user guides and related publications for RUO and IVD/CE-IVD instruments, assays, reagents, and software systems • Work closely with scientists, engineers, quality, regulatory, and product teams to translate complex sequencing technologies and clinical studies into high-quality documentation for internal and external stakeholders • Collect, analyze, and synthesize information from a wide variety of technical and scientific sources and translate it into clear, concise, and user-focused documentation • Author, edit, and maintain documentation supporting clinical sequencing products and workflows, including user guides, technical manuals, SOPs, and internal process documentation • Serve as a strong advocate for clarity, consistency, and usability of technical content in cross-functional program team meetings • Lead documentation-related decision-making for product commercialization, including coordination with legal, regulatory, quality, graphics, style standards, translations, and document control functions • Collaborate with subject matter experts across R&D, bioinformatics, software, quality, regulatory affairs, manufacturing, and product management to ensure technical accuracy and compliance • Manage multiple documentation projects or workstreams, including schedules, priorities, dependencies, and deliverables • Ensure documentation aligns with applicable regulatory and quality requirements and supports audits, submissions and inspections • Train, mentor, and coach other writers within the Technical Communications team; contribute to documentation standards, templates and best practices • Stay current with life sciences industry standards, regulatory expectations, and competitor documentation practices to continuously improve content quality and effectiveness