Technical Writer - Medical domain - Contract (1 Year)

Job Requirements

• Seeking a detail-oriented and experienced Technical Writer with a strong background in the medical domain.

• The candidate will be responsible for creating, editing and managing high quality documentation that meets regulatory and end-user needs.

• Develop, write and maintain clear and accurate documentation, including user manuals, technical specifications, training materials and regulatory documents.

• Collaborate with SMEs, product managers, software/ hardware, QA and regulatory teams to gather and validate information.

• Ensure all documentation complies with applicable medical device regulations and standards (eg: FDA, EU MDR, IEC 62304, IEC 60601 etc )

• Maintain version control and documentation libraries using appropriate tools and systems

Work Experience

• 5 to 10 Years of experience in technical writing with medical domain experience.

• Medical device applicable for FDA. EU MDR regulations.

• IEC 60601, IEC 62304 applicable devices.

• Extensive knowledge and experience in creating technical documents like User manuals, Service manual, IFUs (Instructions for Use)

• Proficient in authoring tools such as MS Word

• Excellent written and verbal communication skills

• Ability to collaborate with multiple project teams and work in tight deadlines