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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.
- 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.
- 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.
- ID: #43677419
- State: Delaware Newark 19702 Newark USA
- City: Newark
- Salary: $35 hr
- Job type: Contract
- Showed: 2022-06-29
- Deadline: 2022-08-27
- Category: Writing/editing