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We are looking for a Technical Writer to produce high-quality global policies and procedures to be used across all Client sites, businesses and regions. The writer will work with the Global Process Owner and development teams to define the process and then outline the process according to standardized formats and structure. Additionally, the role will support document management process.
Job Responsibility:
Develop, manage, and execute a documentation project from initiation through delivery: Analyze the request, create draft documents in active voice and revise according to feedback
Create global policies, procedures, work instructions, forms, technical standards based on input from GPO and process teams using templates and style guides
Partner with GPOs and teams to ensure that procedures accurately reflect the desired end state process
Estimated 85% original writing/15% revisions
Provide support to document control team for release of global documents
Prepare document package for routing and approval in electronic document management system
Process document package in e-DMS
Requirements:
Proven experience working in technical writing position
Experience in writing documentation for the medical device industry according to the Quality Systems Regulation and/or ISO 13485 is required
Experience working with electronic documents management system
Ability to deliver high quality documentation paying close attention to detail
Ability to quickly grasp complex technical concepts and make them easily understandable in text and pictures
Excellent written skills in English – Writing samples may be required upon request
Strong working knowledge of Microsoft Office Suite
BA/BS required with 2 years of business experience, or without BA/BS degree, 5+ years extensive experience in the applicable area