Technical Writer

Company Overview

View Ray Systems, Inc. is a private technology company seeking to provide the global radiation therapy community with advanced medical instruments incorporating the highest level of technology possible. Our belief is that only significant technological innovation can enable society to conquer disease. Our mission is to dare to change the paradigms of medicine and solve “impossible” technical problems to enable clinicians to effect a cure to save precious human lives, mitigate pain and suffering, and enhance quality of life.

Our vision is to become the world’s leader in producing highly effective innovative technology to cure cancer.

View Ray Systems designs, manufactures, and markets the MRIdian A3i® radiation therapy system to treat cancer patients with the smallest radiation therapy margins availablei with the highest patient throughput demonstrated for the most complicated casesii The system treats by aligning the sharpest radiation therapy beam on the market to diagnostic quality magnetic resonance images (MRIs) of the patient, adapts the treatment plan to the reality of the patient, and then uses the real-time MRIs to control the beam and record real-time doses delivered to the patient.

View Ray Systems, Inc. is looking for a Technical Writer that shares our passion for conquering cancer and help us support radiation therapy systems worldwide. The ideal candidate shares enthusiasm for engaging in the best business practices while improving cancer therapy. You will be assisting with radiation therapy user manuals & documentation.

• Creates and maintains manuals detailing Usage, Installation, Operation, Quality Assurance, Servicing, and other topics.
• Manages the translation/localization process of manuals and software interfaces.
• Understand validation and design change control; assist the Product Development team in completing related formal documentation.
• Work cross-functionally within the Engineering teams to acquire source material and to stay knowledgeable about products and procedures.
• Coordinate user validation with Marketing to ensure product labeling is clear and accurate.
• Work with Technical Documentation Coordinator to manage, format, and store documents.
• Work with the Regulatory Affairs/Quality Assurance team to assemble 510(k) submissions according to FDA guidelines.
• Other tasks assigned by company management.

• 5+ years in FDA-regulated, medical device, software development, and manufacturing environments required.
• Experience communicating complex information to an array of audiences, both internal and external.
• Proficiency with electronic publishing and creative applications, particularly Adobe Frame Maker, InDesign, Illustrator, and Photoshop; comfort with Microsoft Office products.
• Coursework in Technical Writing or equivalent experience preferred.
• Ability to work independently to develop content.
• Strong ability to seek information based on initial direction and on project objectives.
• Ability to read, interpret, and apply technical material.
• Ability to take constructive criticisms and guidance.
• Excellent proofreading, English grammar, spelling, and punctuation skills.
• Highly organized, able to handle multiple tasks at the same time.
• Familiarity with localization of content.

• Creative, flexible, and collaborative in approach to technical problem solving.
• Ability to communicate effectively, both orally and in writing, at a variety of technical levels.
• Ability to work effectively as part of the diverse team including physicists, scientists, and engineers in a fast-paced environment and with multiple projects.

Job Type: Full-time

Work Location:

In person in Cleveland, OH:
Relocate before starting work

Salary:
Commensurate with experience

Paid time off

View Ray Systems, Inc. is an Equal Opportunity Employer and does not discriminate on the basis of race, religion, color, creed, national origin, gender, age, sexual orientation, status as a protected disabled or Vietnam Era Veteran, disability, or any other legally protected status.

Reference:

• Mid-Senior level

• Full-time

• Marketing, Public Relations, and Writing/Editing

• Medical Equipment Manufacturing