Description:
Technical Writer/Editor is be responsible for producing high quality documentation appropriate to its intended audience. Candidates preferably reside within a 2 3hour drive of our Tarrytown NY or Newark DE sites to attend onsite meetings when needed.
Your role:
1. analyze existing standard and potential content focusing on reuse and singlesource opportunities.
2. responsible for product labeling for immuno and chemistry assays.
3. will join a team of talented tech writers who work collaboratively with crossfunctional teams to make our products easier to use.
4. will work with internal teams to obtain an indepth understanding of the product(s).
Competencies and Key Skills:
Excellent oral and written communication skills including the ability to articulate clear messages from complex data/information.
Desktop Publishing and Content Management System experience.
Must have strong collaboration skills ability to interface with crossfunctional teams.
Knowledge of the structure and content of the English language including the meaning and spelling of words rules of composition and grammar.
Understanding of clinical data and reports a scientific background knowledge is a plus.
Ability to learn and utilize computer in standard business applications including electronic document control word processing spreadsheets and databases.
High ethical standards.
Highly organized with ability to prioritize own tasks as well as those of others.
Strong interpersonal skills.
Ability to work effectively virtually in conducting internal and external business.
Your expertise:
Technical Writing Certification (preferred)
Science degree or experience in academic settings or as a Medical Technologist a plus
Minimum 5 years direct work experience technical writing in a medical device manufacturing company
Minimum 5 years experience with XMLbased content management system (or equivalent) Abode Frame Maker and In Design intermediate level
Experience working in the InVitro Diagonostic industry highly preferred.