Technical Writer for Preclinical Engineering – Plymouth, MN

Techlink Systems Inc is seeking a skilled Technical Writer for Preclinical Engineering to join our team on a contract basis in Plymouth, MN. This role is vital in documenting complex preclinical engineering processes, ensuring clarity, accuracy, and regulatory compliance within the life sciences industry. Key Responsibilities Create, edit, and maintain high-quality technical documents such as 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 documentation for accuracy, clarity, and adherence to regulatory standards, ensuring consistent messaging. Manage and organize documentation using best practices to keep materials up-to-date and easily accessible. Conduct thorough research to synthesize complex technical information into clear, digestible content. Engage in cross-departmental projects to align technical and non-technical teams. Evaluate existing documentation and recommend improvements to enhance quality and compliance. Required and Preferred Qualifications Bachelor’s degree in Technical Communication, Engineering, Life Sciences, or a related field. Proven experience in technical writing with a strong portfolio demonstrating expertise. Proficiency in Microsoft Word and Excel for document creation and data presentation. Exceptional writing, editing, and communication skills with meticulous attention to detail. Experience with document management systems and regulatory compliance in preclinical research. Excellent collaboration skills to work effectively across departments. Location: Plymouth, MN, USA Job Type: Contract Pay Rate: $40 per hour Remote Eligible: No