Technical Writer

This is 100% remote but candidates need to reside within a 2 3-hour drive of our Tarrytown, NY or Newark, DE sites to attend on-site meetings when needed.

Successful candidate must have technical writing certificate and possess Associate Degree at minimum. Minimum 5 years of field experience in a medical device company is required.

Description :

Technical Writer / Editor is being responsible for producing high quality documentation appropriate to its intended audience.

Expertise Require :

• Minimum of technical writing certificate and Associate’s degree. Bachelor's degree not required.
• Minimum 5 years'' direct work experience technical writing in a medical device manufacturing company
• Minimum 5 years'' experience with XML-based content management system (or equivalent) Abode Frame Maker and in Design, intermediate level
• Experience working in the in Vitro Diagonostic industry highly preferred.
• Science degree or experience in academic settings or as a Medical Technologist a plus
• Desktop Publishing and Content Management System experience.
• Understanding of clinical data and reports, a scientific background knowledge is a plus.

Your role :

• Analyze existing standard and potential content, focusing on reuse and single-source opportunities.
• Responsible for product labeling for immuno and chemistry assays.
• Will join a team of talented tech writers who work collaboratively with cross-functional teams to make our products easier to use.
• Will work with internal teams to obtain an in-depth understanding of the product(s).

Competencies and Key Skills :

• Excellent oral and written communication skills, including the ability to articulate clear messages from complex data / information.
• Must have strong collaboration skills, ability to interface with cross-functional teams.
• Knowledge of the structure and content of the English language including the meaning and spelling of words, rules of composition, and grammar.
• Ability to learn and utilize computer in standard business applications including electronic document control, word processing, spreadsheets and databases.
• High ethical standards.
• Highly organized, with ability to prioritize own tasks as well as those of others.
• Strong interpersonal skills.
• Ability to work effectively virtually in conducting internal and external business.
• Only those lawfully authorized to work in the designated country associated with the position will be considered.
• Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.

Benefits :

For information and details on employment benefits offered with this position, please visit

here

Should you have any questions / concerns, please contact our HR Department via our secure

website

California Pay Equity :

For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website

here

Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law.

Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise,

please contact our HR Department

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.

S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13 / 10-91.).