Technical Writer Iv

Job Description

• Research, write, edit technical documentation to support new and sustaining product development projects.
• Collaborate with development engineering, marketing, regulatory affairs, and clinical, among others, to gather inputs for IFUs.
• Follow internal processes and procedures.
• Understand and comply to medical device regulatory requirements related to labeling.
• Technical aptitude for learning new tools and systems.
• Ability to work in a fast-paced and changing environment.
• Experience / familiarity releasing documentation in Document Control system.
• Very high-level attention to detail.
• Requires a Bachelor's Degree in a relevant technical discipline, Communications, Science, English or equivalent.
• Must have a minimum of two to six plus years of progressively more responsible experience as a technical writer in a medical or high-technology (preferably biotechnology) environment.
• Experience working in a content management system required.
• Must have current or recent medical device or pharma industry experience.
• Must have 2-6 years of experience in the medical device industry.
• Must have end-user technical writing experience; that is, direct experience writing clinician and/or patient manuals.

Top qualities:

• Attention to detail
• Self-starter, manage own projects, no handholding
• Learns tools quickly; content management a plus
• Able to juggle multiple projects at once
• Working with project teams