Specialist Technical Writing

Role & responsibilities:

Review and peer-edit the work of other writers to ensure high quality standards within the technical writing group

Interface cross-functionally within the projects team - and throughout the company - to acquire source material/information for medical device deliverables

Experience creating content within the confines of a department style guide

Preferred candidate profile:

Strong writing, editing and communication and presentation skills to communicate routinely electronically or via phone with cross functional team members.

Applies continuous improvement principles in development of the quality system.

Driven, energetic, self-assured professional with high personal integrity.

Certification as an Internal Quality Auditor will be preferred.

Experience with Windchill Product Data Management systems and Cognition Cockpit

Demonstrated knowledge of the global regulations governing medical device labeling.

Experience working with document translations.

Document and Record Control experience.

Proficiency with Microsoft Office suite.

Experienced in process-based work culture.

Tools:

Windchill Product Data Management systems

Certification as an Internal Quality Auditor

Frame maker, Arbortext editor adobe in Design

Key Skills:

Global regulations governing medical device labeling.

high quality standards within the technical writing group

document translations, Record Control activities