Technical Writer

About the Role

We are seeking a Technical Writer to support documentation creation and management within a regulated environment. This role is ideal for someone detail-oriented with a strong understanding of medical terminology and technical documentation processes.

Key Responsibilities

• Create, edit, and maintain CAPA documentation
• Ensure all documentation complies with FDA regulations
• Collaborate with cross-functional teams to gather and validate information
• Review, standardize, and proofread documents to ensure clarity, accuracy, and consistency
• Manage document version control, archives, and support translation projects

Required Qualifications & Skills

• Bachelor’s degree in Communications, Biomedical Engineering, or a related scientific field
• 1–3+ years of experience in technical writing, preferably in medical device, pharmaceutical, or clinical environments
• At least 1 year of experience working with CAPA documentation
• Strong understanding of medical terminology, including orthopedics, anatomy, and physiology
• Excellent written communication skills with the ability to simplify complex concepts
• High attention to detail and commitment to accuracy