Technical Writer for Preclinical Engineering - Plymouth, MN

Techlink Systems Inc is seeking a skilled Technical Writer for Preclinical Engineering on a contract basis in Plymouth, MN. Join our innovative team focused on advancing life sciences research and development. This role is essential for documenting complex preclinical engineering processes with clarity and regulatory compliance. 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 documents for accuracy, clarity, and adherence to regulatory standards, ensuring consistent messaging across all materials. Manage and organize documentation using best practices to keep materials up-to-date and easily accessible. Conduct thorough research to synthesize complex 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 technical writing experience with a strong portfolio. Expertise 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 with diverse teams. Location: Plymouth, MN, USA Job Type: Contract Pay Rate: $40 per hour Note: This position is not eligible for remote work.