Senior Associate Scientist, Scientific Writing

Senior Associate Scientist, Scientific Writing Columbus, Ohio Forge Your Future with Us: At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is simple yet powerful: to enable access to life-changing gene therapies and help bring them fromideainto reality. We partner with scientists, physicians, biotech and pharma innovators, and patient communities — all united by one goal: improving lives. Ifyou’redriven by purpose and excited to make a tangible impact, this is where your journey begins. Our team works out of The Hearth,a state-of-the-art, 200,000-square-foot cGMP facility in Columbus, Ohio. Here, youwon’tjust watch innovation happen —you’llbe part of it. Whetheryou’rescaling AAV manufacturing, collaborating oncutting-edgetherapies, or supporting complex technical projects,you’llplay a key role in bringing hope to patients with genetic diseases. What sets Forge apart is our culture of H.O.P.E. We are hardworking , showing up each day with determination and grit. We are open , creating a space where ideas flowfreelyand every voice is valued. We are purpose-driven , with every task directly tied to changing lives. And we are engaged , energized by the challenges we face and the milestones we achieve together. At Forge, your growth matters.We’recommitted to helping you expand your skills, take on new challenges, and develop your career through mentorship, hands-on learning, and opportunities for advancement. Our people are our greatest investment, andwe’reproud to see team members grow with us. Ifyou’reready to use your talent to help deliver hope to patients around the world, join us — and be part of something bigger than yourself. About The Role: TheSeniorAssociate Scientist, ScientificWritingindependently leads documentation projects acrossoperational, analytical,microbiological,andstabilityfunctions within QC. This role requires deeper collaboration withsubject matter experts across all departments and QC team members of all levels. Responsibilities: Works with cross-functional teams with guidance from direct supervisor and senior team members to d evelop and maintain high-level technical and scientific documents, including S tandard operating procedures for the QC group P rotocols and reports using established templates Owns and manages documentation projects by participating in cross-departmental conversation s to ensure alignment with QC requirements Assists SMEs and development teams through updates driven by method qualification, continuous improvement , or change controls R eviews documentation for quality, and ensures alignment across client deliverables Collaborates with SMEs to identif y gaps in documentation and fill those gaps with clear, accurate information Organize information from multiple sources impacting documentation Demonstrates fluency in Veeva Vault and communicates with system owners to ensure process continuity Qualifications: Bachelor’s degree in a science field with 2-3 years of experience, or Master’s in a science field with writing experience Demonstrated leadership, strategic thinking Proven ability to manage ambiguity, lead complex projects, and influence cross-functional teams Experience authoring complex technical documents K nowledge of complex molecular biology, biochemistry, or cell biology techniques and analytical methods (e.g., qPCR, cell-based infectivity assays, potency assays) Exper ience in scientific communication Skilled in managing multiple document types and priorities simultaneously Excellent written, verbal, and project coordination skills High proficiency in documentation systems, formatting tools, and visualization software Preferred Skills: Previous exposure regulatory guidelines (ICH, FDA, EMA) Experience mentoring or training junior teammates Proficiency with Smartsheet, Veeva Vault, SmartDraw, Visio, Adobe Acrobat, or similar tools Expertise in software tools such as Veeva Vault, SmartDraw, Visio, and Adobe Acrobat Strategic thinking with a continuous improvement mindset related to document systems and compliance At Forge Biologics, we believe our people deserve to be taken care of — in and out of the workplace.We’vebuilt a comprehensive compensation and benefits package designed to help you thrive, grow, and feel valued every step of the way: Health from day one Health, dental, and vision insurance start your first day — with 90% of premiums covered for you and your family. Time to recharge A competitive paid time off plan — because rest fuels innovation. 12 weeksof fully paid parental leave so you can focus on family when it matters most. Rewarding your impact Annual bonus opportunities for all full-time team members. 401(k) with company match to help youplan for the future. Special employee discounts, including childcare and dependent care savings. Onsite fitness facility at The Hearth Mental health counseling and financial planning services through our Employee Assistance Program. Employer-paid short- and long-term disability coverage to protect your peace of mind. Fuel for your workday A fully stocked kitchen with free snacks and beverages — we keep you energized and ready forwhat’snext. Grow with us Ongoing professional development resources, training opportunities, and mentorship programs to help you build your career and grow within Forge. Create a Job Alert Interested in building your career at Forge Biologics? 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