Technical Writer for Preclinical Engineering - Plymouth, MN

Techlink Systems Inc is seeking a skilled Technical Writer for Preclinical Engineering to join our Plymouth, MN team on a contract basis. This role is integral to documenting complex preclinical engineering processes within the life sciences industry, ensuring clarity, accuracy, 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 project requirements and technical specifications.
• Review documentation for accuracy, clarity, and adherence to regulatory standards while maintaining consistent messaging.
• Manage and organize documentation using best practices to ensure materials are current and accessible.
• Conduct thorough research to translate 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 related field.
• Proven technical writing experience with a strong portfolio.
• Proficiency in Microsoft Word and Excel for document creation and data presentation.
• Excellent writing, editing, and communication skills with meticulous attention to detail.
• Experience with document management systems and regulatory compliance in preclinical research.
• Strong collaboration skills to work effectively across departments.

Location: Plymouth, MN, USA
Employment Type: Contract
Pay Rate: $40 per hour