Technical Writer/Editor 3

at VIVA USA Inc. in Newark, Delaware, United States

Job Description


This is a role well suited to an ambitious professional, looking for the next step in their career.

As an InDesign Technical Writer/Editor, you will be responsible for:

Developing content for instructions for use.
Demonstrate proficiency and provide leadership through the content development process to meet company strategies and business objectives.
Oversee the correct, complete, and compliant execution of product instructions for use and resolve problems and exceptions.
Develop and maintain labeling procedures that comply with FDA, GMP, ISO and other applicable standards and regulations.
Assure all activities comply with established SOPs, best practices, and GMPs.
Identify and lead process for obtaining feedback from key stakeholders for continuous improvements to content development process.
Drive continuous improvements through observation, measurement, and root cause analysis/resolution.
Develop and maintain tools to manage label team workflow.
Performs additional duties or assignments as directed by management.

This position may suit you best if you are familiar with what is below :

Scientific background knowledge, understanding of data and reports.
A medical writer or medical technologist skills
Proven experience in use of InDesign; XML experience is a plus
Excellent verbal and written communication skills
Must have strong collaboration skills, ability to interface with cross functional teams.

Required skills to have for the success of this role:

Bachelor’s degree or equivalent experience required
Minimum 5 years’ direct work experience as a technical writer in a medical device manufacturing company.
Minimum 5 years’ experience with InDesign; additional XML-based content management system experience a plus.
Experienced technical writer with proven ability with InDesign

Note :

9:00 am to 5:00 pm
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Job Posting: 986989

Posted On: Jun 13, 2022

Updated On: Jul 13, 2022