Technical Writer Intern

Job Description

Job Title: Technical Writer Intern – Regulatory & Engineering Documentation Location: Chennai, India (Onsite – IIT Madras Research Park) Employment Type: Internship (6 months, fixed) Stipend: ₹10,000 – ₹20,000/month Requirement: Bachelor's/Masters in Mechanical, electronics, biomedical engineering 🧬 About Floaid Floaid is a MedTech startup pioneering next-generation cardiac assist technologies. We work at the intersection of innovation, precision engineering, and regulatory compliance to create life-saving medical devices. 🔍 Role Overview We are seeking a detail-oriented Technical Writer Intern to support our multi-disciplinary engineering and regulatory teams. You will be responsible for preparing technical documentation, regulatory filings, literature reviews, and professional presentations. This role is critical in ensuring high-quality, accurate, and compliant documentation across mechanical, electronics, and clinical domains. 🛠️ Key Responsibilities Draft and maintain technical documents for mechanical, electronics, software, and system-level subsystems Assist in preparing regulatory documents for CDSCO, ISO 13485, IEC 60601, and FDA submissions Conduct literature reviews and compile research summaries for product validation Create PowerPoint presentations for investor meetings, audits, and internal reviews Work closely with R&D, Regulatory Affairs, and Quality teams to ensure content accuracy and version control Organize internal documentation in line with ISO/document control standards Support in writing SOPs, user manuals, risk analysis, and design history files (DHF) ✅ Requirements Completed a degree in Biomedical Engineering, Mechanical Engineering, Electronics, Biotechnology, or related technical field Excellent written and verbal communication skills in English Familiarity with regulatory standards (preferred: ISO 13485, IEC 60601, MDR, FDA) Strong skills in MS Word, PowerPoint, and Google Docs/Sheets Ability to quickly learn technical concepts and convey them in simple language Highly organized with attention to detail Passionate about innovation in healthcare 🌱 What You’ll Gain Real-world exposure to MedTech product development and regulatory frameworks Hands-on experience in interdisciplinary technical documentation Mentorship from domain experts in biomedical engineering and regulatory affairs Opportunity to convert into a full-time role based on performance To Apply: Via Linkdin Show more Show less