Hologic is a global medical device company that specializes in women's healthcare. Hologic empowers people to live healthier lives everywhere, every day.

Discover a rewarding career with real meaning. One that offers the opportunity to showcase your talents, achieve measurable success, and gain immense satisfaction by enabling healthier lives everywhere, every day.

Our Breast & Skeletal Health is looking for a Technical Writer II to support BSH, Tech Pubs team, within the labeling Center of Excellence (COE). As a Technical Writer, you will be responsible for developing, designing, and controlling instructional and informational tools to ensure the safe, appropriate, and effective use of science and technology, intellectual property, and manufactured products and services. This position will either be at our expanding Innovation Center in Newark, DE, or our headquarters in Malborough. It is a hybrid position that is 2-3 days onsite.

Apply today! 

What To Expect:

 Design and implement work instructions, area guidelines, knowledge base topics, and departmental SOPs as required.

• Create new documentation and improve existing documentation. 
• Work with key personnel to expand knowledge and understanding of how to perform and troubleshoot instrumentation, assays, software, etc. to develop and improve content.
• Identify and implement document changes to maintain consistency across product lines/processes.
• Lead collaborative review sessions and cross-functional team Label Design Review.
• Manage multiple user documentation projects at a time.
• Assist core team members and project team leads in the developing documentation timelines and deliverables.
• Initiates and drives inter-departmental continuous improvement for a team of contributors.
• Works towards obtaining certification relevant to job functions.
• Information Design and Development.
• Work with the international/translation Labeling Coordinator, addressing questions from the vendor.
• Contribute to work instructions, area guidelines, knowledge base topics, style guides/templates, and department SOPs.
• Attend project/core team meetings as required as an extended core team representative and make recommendations regarding the IFU project schedule and deliverables, considering information learned at these meetings.
• Revise existing documentation by working w/ stakeholders, partners, or distributors to facilitate revision, review and approval of documentation. 
• Coordinate the collaborative review process and establish review and edit cycles based on the project timeline and resource availability. Train the cross-functional team on the review process as needed.
• Coordinate the transition of documentation through preproduction, regulatory submission, and production phases as appropriate. 
• INVs/CAPA investigations using analytical skills and judgment, conferring with other writers and SMEs when appropriate, to determine root causes and to recommend and implement changes.
• Through Technical Training, maintain and expand knowledge of assays, instrumentation, and software as they apply to documentation. 
• May, on special occasions, coordinate and manage translation projects to assist the International Labeling Coordinator.
• Initiates and drives departmental continuous improvement for a team of contributors.

What We Expect:

• Experience with PLM systems such as Agile
• Problem Solving and Analytical Skills
• Project and Time Management Skills
• Intermediate Technical Writing Theory and Practices 
• Design Theory 
• Troubleshooting Skills
• Interpersonal skills
• Technical skills: Adobe Suite InDesign, Illustrator, Adobe Pro… MS Office applications
• MadCap Flare, and Author-It a plus
• Experience with HTML and CSS a plus
• Experience with source control such as Team Foundation Server and GitHub a plus

5-8 years related experience.