Integrated Resources
Technical Writer - Assay Development
Integrated Resources, Tucson, Arizona, United States, 85718
This is an onsite position supporting Product Development.
The primary responsibility of this position is to act as the Technical Writer on project teams, attend meetings, and update the supervisor. Involved in the creation, review, revision and approval of documentation and labeling for Tissue Diagnostics products.
SKILLS, EXPERIENCE & EDUCATION --3-5 years of direct documentation experience in medical device, software, pharmaceutical, or biotechnology industry --Knowledge of current US and International regulations as they pertain to documentation (e.g., FDA, ISO, IVDD and 21 CFR 11), and control of electronic records --Demonstrable record of working on project teams while working on multiple projects --Experience with international regulatory requirements (preferred) --Bachelor's degree in a scientific discipline or other related technical field
SKILLS, EXPERIENCE & EDUCATION --3-5 years of direct documentation experience in medical device, software, pharmaceutical, or biotechnology industry --Knowledge of current US and International regulations as they pertain to documentation (e.g., FDA, ISO, IVDD and 21 CFR 11), and control of electronic records --Demonstrable record of working on project teams while working on multiple projects --Experience with international regulatory requirements (preferred) --Bachelor's degree in a scientific discipline or other related technical field