Technical Writer for Preclinical Engineering

At Techlink Systems Inc, a leader in advancing life sciences research and development, we're looking for a skilled Technical Writer for Preclinical Engineering to join our Plymouth, MN team on a contract basis. This role offers a unique opportunity to contribute to cutting-edge preclinical projects that impact healthcare innovation. You'll be part of a dynamic environment where your documentation expertise ensures regulatory compliance and clarity in complex technical processes. Join us to advance your career in a growing company that values precision, collaboration, and professional growth. This is an on-site position, ideal for candidates eager to engage directly with R&D teams and influence critical documentation standards. Key Responsibilities Create and maintain detailed technical documents such as user manuals, SOPs, and regulatory submissions that meet industry standards and FDA guidelines. Collaborate closely with R&D engineers and scientists to accurately capture project requirements and technical specifications. Review and edit documentation for clarity, accuracy, and regulatory compliance, ensuring consistent messaging across all materials. Manage document control systems to keep all files current, organized, and accessible to relevant stakeholders. Conduct thorough research to translate complex preclinical engineering concepts into clear, user-friendly content. Engage in cross-functional projects to align documentation with both technical and non-technical team needs. Evaluate existing documentation and recommend improvements to enhance usability and compliance. Ensure adherence to regulatory standards such as GLP and FDA 21 CFR Part 11 throughout documentation processes. What We're Looking For Required: Bachelor’s degree in Technical Communication, Engineering, Life Sciences, or related field. Proven experience as a technical writer with a portfolio demonstrating complex document creation in regulated environments. Proficiency in Microsoft Word and Excel for document creation and data presentation. Strong writing, editing, and communication skills with meticulous attention to detail. Experience with document management systems and knowledge of regulatory compliance in preclinical research. Ability to collaborate effectively with multidisciplinary teams. Preferred: Familiarity with preclinical engineering processes and life sciences industry standards. Experience working within FDA-regulated environments. Knowledge of additional documentation tools such as Adobe FrameMaker or MadCap Flare. Strong organizational skills and ability to manage multiple projects under tight deadlines. What We Offer Competitive pay at $40 per hour with contract flexibility. Health insurance options to support your well-being. Paid time off to maintain work-life balance. Retirement plan opportunities to secure your future. Professional development programs to advance your technical writing skills and industry knowledge. Collaborative work environment with access to cutting-edge research projects. On-site engagement fostering direct interaction with R&D teams and leadership. Frequently Asked Questions Is this position remote or on-site? This role is strictly on-site at our Plymouth, MN location to facilitate close collaboration with R&D teams. What is the expected contract duration? The contract length will be discussed during the interview process, with potential for extension based on project needs. What software tools will I be expected to use? Proficiency in Microsoft Word and Excel is required; experience with document management systems and tools like Adobe FrameMaker is a plus. Are there opportunities for career advancement? Yes, Techlink Systems values career development and offers professional growth opportunities within technical writing and related fields. What regulatory standards should I be familiar with? Knowledge of FDA regulations, GLP, and 21 CFR Part 11 is essential for ensuring compliance in documentatio