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Produce clear, concise, and understandable technical documentation that meets the needs of different user groups, from general users to healthcare professionals.

Actively participate in new product development and sustaining product meetings to provide insights on best quality outcomes for instructional material strategies and resolve related challenges.

Oversee and provide recommendations for the development of formats and guidelines for documentation.

Ensure effective planning and management of timelines for all aspects of technical documents.

Collaborate extensively with all key cross-departmental teams to finalize inputs for changes to product content.

Work effectively and efficiently in a high production environment and deftly switch between projects as priorities shift.

Develop, write, edit, and revise product documentation including Operating Instructions, Technical Manuals, Setup Guides, and Instructions for Use (IFUs) that provide instructions and information detailing user/patient safety, product features, procedures for handling, maintenance, etc.

Organize content and complete writing assignments according to established guidelines for order, content, clarity, conciseness, format, style, and terminology.

Conceptualize graphical elements (tables, charts, illustrations, etc.) that support instructional information.

Collaborate with label/marking designers to align labeling and product documentation content.

Assist with product label updates using Adobe Illustrator.

Support translation efforts to enable global product reach.

Utilize change management systems for product deliverable releases/updates.

Help establish standardized text, glossaries and nomenclature, style guides and templates, and structure of instructional information.

Initiate and/or support continuous improvement initiatives within the functional area.

Provide and support cross-training of team members through guidance, feedback, and knowledge sharing.

Qualifications:

Bachelor's degree in engineering, business, technical writing, or a related discipline with a strong emphasis on communication skills preferred.

2+ years of experience in a medical device, pharmaceutical, or similarly regulated environment preferred.

Knowledge of Adobe InDesign and Illustrator is required.

Experience with product label design and updates preferred.

Experience in translations is strongly preferred.

Author-it experience is a plus.

Proficiency in Microsoft Office tools.

Experience with Jira and Windchill is a plus.

Working knowledge of FDA and MDR labeling requirements preferred.

Knowledge of printing and graphic reproduction practices preferred.

Knowledge of XML authoring tools and XML publishing using CSS preferred.

Knowledge of a variety of writing formats including print, web, and multimedia desired.

JOBID: JN - 012026-120734#LI-CELLA#LI-AV1#PLEqual Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Cella, a randstad digital company, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [email protected] offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Cella by randstad digital offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days.