| Job Description | The Company is a pioneer in medical robotics and world leader in image-directed, robotic products for orthopedic applications. The Company’s product allows surgeons to pre-operatively plan their surgery in a 3-D virtual space and then execute the surgery in the operating room, exactly as planned.
The scientific technical writer develops, writes, and edits material for customer manuals, release notes, submissions, clinical documentation, web content, sale collaterals and internal procedures as required. The writer must be able to effectively translate highly technical information into end-user appropriate language without sacrificing technical accuracy. The writer will utilize functional specifications, access medical equipment, and interface with engineers, surgeons and others as applicable to develop content. The technical writer ensures documents meet the company’s high standards for technical and regulatory accuracy, clarity, tone, and style while adhering to aggressive timelines. The writer must also be an experienced project manager, able to represent their area on cross functional teams while managing multiple writing projects simultaneously.
Travel Requirements:
?10% Training opportunities and/or medical sites.
Job Responsibilities:
?Compose medical reports, presentations and other comprehensive materials using correct grammar, punctuation, spelling editing, formatting, and proofreading skills to clearly and concisely provide accurate information.
?Maintain Product User Manuals.
?Assist in writing summaries for regulatory submissions, engineering and clinical reports.
?Maintain web content and sales collaterals.
Qualifications
?A life science degree is absolutely essential.
?Minimum five (5) years experience within the medical device industry writing/editing scientific/medical material.
?Adobe CS version 5 or 6 prefer.
?Excellent oral/written communication, research, and interpersonal skills required.
?Strong engineering acumen with the ability to read and decipher specs, blue prints, and other technical documents to create end-user friendly procedures.
?Excellent project management skills, including participation on cross functional teams
?Detail-oriented, including the ability to follow directions precisely.
?Excellent organizational, analytical, and problem solving skills.
?Must also be able to work independently on a multiple task work load and produce a quality product under a tight time constraint. Highly proficient with MS Office, Webworks, RoboHelp desirable.
?Knowledge of Good Manufacturing Practices (GMP) and applicable Quality System Standards.
?Attendance and Punctuality are essential function of the position. |
| | Company | | Curexo Technology Corporation | Job Code | | State or Province | | California | | |
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