Technical Writer - Medical domain - Contract (1 Year)
QuEST Global
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 WordExcellent written and verbal communication skillsAbility to collaborate with multiple project teams and work in tight deadlines
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 WordExcellent written and verbal communication skillsAbility to collaborate with multiple project teams and work in tight deadlines
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