Technical Writer

Duration: 12 months with possible conversion Compensation: $34-$40 hourly rate Job Description Our client is looking for a Technical Writer II to join a leading medical device manufacturing company to be responsible for developing, editing, and maintaining high-quality Instructions for Use (IFUs) and labels that support clinician use, patient safety, and regulatory compliance. The ideal candidate is detail-oriented, collaborative, and skilled at translating complex technical information into clear, user-focused content. Responsibilities Writing: Exceptional writing and communication skills. Document Authoring: Create and update clinician IFUs, patient manuals, and product labels. Cross-Functional Collaboration: Lead documentation reviews with engineering, quality, clinical, regulatory, marketing, and manufacturing teams to ensure technical accuracy and regulatory compliance. Regulatory Compliance: Ensure all materials conform to strict standards including FDA guidelines, ISO norms, and EU MDR requirements. Document Control: Create and maintain precise revision histories and supporting documentation for risk management. Project Management: Create and adhere to project plans for document completion. Manage multiple projects simultaneously as required. Required Skills & Qualifications Education: Bachelor's degree in Technical Communication, English, Biomedical Engineering, or a Life Science discipline. Experience: Minimum of 2+ years of technical writing experience within a regulated, medical, or manufacturing environment. Technical Proficiency: Mastery of tools like Microsoft Office Suite, Adobe Creative Suite, and experience using Content Management and Quality Management Systems. Core Competencies: Exceptional eye for detail, critical thinking, strong cross-functional communication skills, maintenance of effective relationships with subject matter experts, and the ability to simplify dense terminology. Preferred Skills & Qualifications Advanced degree in technical communications, English or similar Document creation using an XML-based content management system Writing for multiple audiences (clinicians and patients) Strong attention to detail Knowledge of medical terminology and anatomy Proven understanding of literature and labeling development in a heavily-regulated environment Use of critical-thinking and problem-solving skills to identify risk and develop creative solutions #J-18808-Ljbffr Insight Global