Collaborate closely with cross-functional teams including software engineers, UX/UI designers, product managers, and regulatory experts to gather information and understand product specifications.
Create user-centric documentation for UI applications, including user guides, instruction manuals, online help systems, and release notes.
Translate complex technical information into easy-to-understand language for end-users, ensuring accuracy and compliance with industry standards and regulatory requirements.
Conduct usability testing and gather feedback to continuously improve the clarity and effectiveness of documentation.
Manage documentation projects from conception to completion, adhering to project timelines and deliverables.
Qualifications:
Bachelors degree in English, Technical Communication, Computer Science, or a related field.
2 to 5 years of experience in technical writing, with a focus on UI applications preferably in the medical device industry.
Strong writing and editing skills with impeccable attention to detail.
Proficiency in documentation tools such as Microsoft Word, Adobe FrameMaker
Experience with version control systems (eg, Git) and content management systems (eg, SharePoint).
Familiarity with Agile development methodologies and the ability to work in a fast-paced, collaborative environment.
Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams.
Nice to Have
Knowledge of regulatory requirements for medical device documentation, such as FDA regulations (21 CFR Part 820) and ISO standards (ISO 13485).
