We are seeking a skilled Technical Writer for Preclinical Engineering to join our team on a contract basis in Plymouth, MN. The ideal candidate will work in a dynamic environment within a reputable company focused on advancing research and development in the life sciences industry. This role plays a crucial part in documenting complex preclinical engineering processes, ensuring clarity and compliance within the regulatory landscape.Key ResponsibilitiesCreate, edit, and maintain high-quality technical documents, including user manuals, standard operating procedures (SOPs), and regulatory submissions.Collaborate closely with R&D teams to gather and understand project requirements and technical specifications.Review documents for accuracy, clarity, and adherence to regulatory standards while ensuring consistency in messaging across all documentation.Manage and organize documentation using best practices for document management, ensuring that all materials are up-to-date and easily accessible.Conduct thorough research to support the creation of content, synthesizing complex information into an easily digestible format.Engage in cross-departmental projects to ensure alignment between technical and non-technical teams.Evaluate and provide feedback on existing documentation, recommending improvements where necessary.Required and Preferred QualificationsBachelor’s degree in a relevant field (e.g., Technical Communication, Engineering, Life Sciences).Proven experience in technical writing with a strong portfolio of work.Expertise in Microsoft Word and Microsoft Excel for document creation and data presentation.Strong writing, editing, and communication skills with meticulous attention to detail.Experience with document management systems and regulatory compliance related to preclinical research.Excellent collaborative skills to work effectively in team settings.This position supports a structured team environment where open communication and collaboration thrive. The Technical Writer will report to the Preclinical Engineering Manager while frequently working with cross-functional teams including research and compliance.Our company fosters a culture of continuous learning and professional growth. You will have the opportunity to engage in various projects that develop your skills and navigate the evolving landscape of preclinical engineering documentation. We offer a modern workplace with flexibility, and promote a healthy work-life balance, allowing professionals to thrive both personally and professionally.