Job Requirements
Project purpose:
Maintenance of manuals and labeling for the Maternal Infant Care group.
CTQ business requirements:
Ensuring all the product manuals and labeling are up to date. Also work with external agencies for translations.
Qualifications/Requirements:
Technical graduation degree with strong technical publication work experience
Must to have skill sets:
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Associates degree (or local equivalent), mechanical, aviation, industrial production, electrical, electronics, bio-medical engineering, science writing, or other related technical discipline or at least 4+ years of experience as a technical writer
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Minimum of 4+ years of technical writing experience
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Familiarity with conventions in form, structure, and notation of technical writing
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Exceptional written, organizational, inter-personal, project management, and communication skills
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Proficiency in Oxygen, or other XML authoring tools, Frame maker, content management systems, Excel, Word, Outlook, Photoshop, Illustration, InDesign, and PowerPoint
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Writing in DITA framework
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Working knowledge of Agile methodologies
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Wide degree of creativity
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Highly motivated with the ability to work well both independently and in a team environment
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Ability to communicate using English (or local language)
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Good to have skill sets:
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Bachelors degree in journalism, technical communication, English, science writing, or other related discipline.
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Writing experience in the medical device industry
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Experience writing user and service documents, and using content management systems and xml authoring tools
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Understanding of the software development cycle
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Functional knowledge in a wide range of technologies such as HTML and VB Script.
Work Experience
Must Have Skills:
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CMS (Content Management System)
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DITA
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Adobe Illustrator
Good to have skills:
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Adobe Framemaker
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Mechanical Engineering Background: helpful to understand device components, workflows and technical terminology
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Fast learner & adaptability: ability to quickly understand new tools, processes and domain knowledge
Essential Responsibilities:
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Research, collect source data, and interview appropriate personnel to compose text for technical literature, which meets GEHC standards and procedures.
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Create, edit, and maintain technical user and service publications that accurately and effectively support the product release requirements in various output formats (pdf, online help, cd, etc.)
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Develop content using a content managements system and xml authoring tool
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Track and fix content defects
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Create documentation methodologies, frameworks, and workflow diagrams
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Coordinate review of all assigned writing projects to ensure thorough documentation
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Provide input on other technical writing projects by critiquing, editing, and proofreading manuscripts prepared by others
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Complete writing assignments on-time and within budget according to departmental and industry standards
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Assist and/or analyze project requirements to determine types or publications needed and develop project plans and timelines
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Contribute to the development and expansion of the department and it’s offerings
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Successfully work with and communicate with global teams
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Assists and develops graphic and illustrations used in user and service documentation
Desired Characteristics:
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Complete all planned Quality & Compliance training within the defined deadlines.
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Identify and report any quality or compliance concerns and take immediate corrective action as required.
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Participate in continuous improvement activities by identifying and appropriately escalating process and product quality gaps, providing solutions when possible.
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Should be able to work late hours as there would be a need to connect with Global counterparts on a regular basis.
Acceptance Criteria:
Provide design output with on time schedule & GE HealthCare quality standards.
Deliverables:
Error-free and on-time completion of the given tasks.